Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25929 |
| ensemblid | ENSG00000082516.9 |
| hgncid | 20043 |
| symbol | GEMIN5 |
| name | gem nuclear organelle associated protein 5 |
| refseq_nuc | NM_015465.5 |
| refseq_prot | NP_056280.2 |
| ensembl_nuc | ENST00000285873.8 |
| ensembl_prot | ENSP00000285873.6 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 154887411 |
| end | 154938211 |
| strand | - |
| ver | v1.2 |
| region | chr5:154887411-154938211 |
| region5000 | chr5:154882411-154943211 |
| regionname0 | GEMIN5_chr5_154887411_154938211 |
| regionname5000 | GEMIN5_chr5_154882411_154943211 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1508 | 245 | 49 | 50 | 101 | 13 | 31 | 70 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0002 | 0/0 | 1508 | 39 | 9 | 13 | 10 | 3 | 4 | 8 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0003 | 1/0 | 1508 | 33 | 15 | 2 | 14 | 0 | 1 | 10 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0004 | 0/0 | 1508 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0005 | 0/0 | 1508 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0006 | 0/0 | 1508 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0007 | 0/0 | 1508 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0008 | 0/0 | 1508 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0009 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0010 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0011 | 0/0 | 1508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0012 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0013 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0014 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| a0015 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | MGQEP others(1503): Show |
chr5 | 154882411 | 154943211 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4524 | 232 | 40 | 49 | 99 | 13 | 30 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0001c0004 | 0/0 | 4524 | 9 | 9 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0001c0014 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0001c0025 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0001c0029 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0001c0030 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0002c0002 | 0/0 | 4524 | 32 | 6 | 11 | 9 | 3 | 3 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0002c0008 | 0/0 | 4524 | 3 | 2 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0002c0011 | 0/0 | 4524 | 2 | 0 | 0 | 1 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0002c0018 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0002c0021 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0003c0003 | 1/0 | 4524 | 17 | 3 | 2 | 10 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0003c0005 | 0/0 | 4524 | 7 | 7 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0003c0007 | 0/0 | 4524 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0003c0009 | 0/0 | 4524 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0003c0015 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0003c0023 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0004c0006 | 0/0 | 4524 | 6 | 6 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0005c0026 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0005c0027 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0006c0012 | 0/0 | 4524 | 2 | 1 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0007c0020 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0007c0022 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0008c0010 | 0/0 | 4524 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0009c0031 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0010c0028 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0011c0019 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0012c0017 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0013c0013 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0014c0024 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 | ||
| a0015c0016 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | ATGGG others(4519): Show |
chr5 | 154882411 | 154943211 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5404 | 193 | 25 | 37 | 99 | 8 | 23 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0001c0001t0002 | 0/0 | 5404 | 36 | 15 | 10 | 0 | 5 | 6 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0001c0001t0003 | 0/0 | 5404 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0001c0001t0006 | 0/0 | 5404 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0001c0004t0001 | 0/0 | 5404 | 8 | 8 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0001c0004t0005 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0001c0014t0001 | 0/0 | 5404 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0001c0025t0001 | 0/0 | 5404 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0001c0029t0002 | 0/0 | 5404 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0001c0030t0001 | 0/0 | 5404 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0002c0002t0001 | 0/0 | 5404 | 32 | 6 | 11 | 9 | 3 | 3 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0002c0008t0001 | 0/0 | 5404 | 3 | 2 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0002c0011t0001 | 0/0 | 5404 | 2 | 0 | 0 | 1 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0002c0018t0001 | 0/0 | 5404 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0002c0021t0001 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0003c0003t0001 | 1/0 | 5404 | 16 | 3 | 2 | 10 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0003c0003t0007 | 0/0 | 5404 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0003c0005t0001 | 0/0 | 5404 | 7 | 7 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0003c0007t0001 | 0/0 | 5404 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0003c0009t0001 | 0/0 | 5404 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0003c0015t0008 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0003c0023t0001 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0004c0006t0001 | 0/0 | 5404 | 6 | 6 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0005c0026t0001 | 0/0 | 5404 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0005c0027t0001 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0006c0012t0002 | 0/0 | 5404 | 2 | 1 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0007c0020t0001 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0007c0022t0001 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0008c0010t0001 | 0/0 | 5404 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0009c0031t0001 | 0/0 | 5404 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0010c0028t0002 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0011c0019t0001 | 0/0 | 5404 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0012c0017t0004 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0013c0013t0001 | 0/0 | 5404 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0014c0024t0001 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| a0015c0016t0001 | 0/0 | 5404 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | GCCCC others(5399): Show |
chr5 | 154882411 | 154943211 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0009 | 0/1 | 3 | 0 | 1 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0003 | 0/0 | 5 | 2 | 0 | 0 | 0 | 3 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0004t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0004t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0004t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0014t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0025t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0029t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0001c0030t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0008t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0008t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0008t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0011t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0011t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0018t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0002c0021t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0003t0001g0004 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0003t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0003t0007g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0005t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0005t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0005t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0005t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0005t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0005t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0005t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0007t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0007t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0007t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0009t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0009t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0009t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0015t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0003c0023t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0004c0006t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0004c0006t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0004c0006t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0004c0006t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0004c0006t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0005c0026t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0005c0027t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0006c0012t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0006c0012t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0007c0020t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0007c0022t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0008c0010t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0008c0010t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0009c0031t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0010c0028t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0011c0019t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0012c0017t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0013c0013t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0014c0024t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| a0015c0016t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0242 | EUR | GBR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0238 | EUR | FIN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0281 | EUR | FIN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00558 | hp2 | a0003 | c0007 | t0001 | g0073 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00621 | hp2 | a0001 | c0014 | t0001 | g0209 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01069 | hp2 | a0005 | c0026 | t0001 | g0103 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01109 | hp1 | a0002 | c0018 | t0001 | g0046 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01243 | hp1 | a0002 | c0008 | t0001 | g0062 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0075 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0060 | EUR | IBS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01891 | hp1 | a0003 | c0005 | t0001 | g0083 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01934 | hp1 | a0001 | c0029 | t0002 | g0277 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0081 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0082 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0074 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02055 | hp1 | a0003 | c0005 | t0001 | g0077 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02055 | hp2 | a0002 | c0008 | t0001 | g0064 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02080 | hp1 | a0009 | c0031 | t0001 | g0069 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02080 | hp2 | a0003 | c0007 | t0001 | g0044 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02129 | hp1 | a0003 | c0007 | t0001 | g0045 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0056 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CDX | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CDX | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0124 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0125 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02280 | hp2 | a0006 | c0012 | t0002 | g0221 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02451 | hp2 | a0003 | c0005 | t0001 | g0087 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02615 | hp1 | a0004 | c0006 | t0001 | g0032 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02630 | hp1 | a0010 | c0028 | t0002 | g0229 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02630 | hp2 | a0001 | c0004 | t0005 | g0039 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02647 | hp2 | a0007 | c0022 | t0001 | g0049 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02698 | hp2 | a0006 | c0012 | t0002 | g0220 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02723 | hp2 | a0003 | c0005 | t0001 | g0078 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02735 | hp2 | a0011 | c0019 | t0001 | g0070 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0090 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02886 | hp1 | a0002 | c0021 | t0001 | g0092 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0089 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02965 | hp1 | a0003 | c0005 | t0001 | g0079 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0119 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02976 | hp1 | a0003 | c0003 | t0001 | g0035 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0088 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03098 | hp1 | a0004 | c0006 | t0001 | g0273 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0122 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03139 | hp2 | a0003 | c0009 | t0001 | g0042 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0126 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03225 | hp1 | a0004 | c0006 | t0001 | g0276 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03225 | hp2 | a0003 | c0009 | t0001 | g0040 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03453 | hp2 | a0012 | c0017 | t0004 | g0279 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0121 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0123 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03516 | hp2 | a0002 | c0008 | t0001 | g0063 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03704 | hp2 | a0001 | c0025 | t0001 | g0178 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03831 | hp1 | a0002 | c0011 | t0001 | g0048 | SAS | BEB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0068 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0214 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18522 | hp1 | a0003 | c0005 | t0001 | g0084 | AFR | YRI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18522 | hp2 | a0004 | c0006 | t0001 | g0274 | AFR | YRI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0086 | EAS | CHB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | YRI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18906 | hp2 | a0007 | c0020 | t0001 | g0065 | AFR | YRI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18939 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18940 | hp2 | a0003 | c0007 | t0001 | g0072 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18949 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18954 | hp2 | a0008 | c0010 | t0001 | g0033 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18956 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18959 | hp2 | a0001 | c0030 | t0001 | g0213 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18964 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18982 | hp1 | a0003 | c0003 | t0001 | g0269 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19000 | hp1 | a0013 | c0013 | t0001 | g0118 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19001 | hp2 | a0008 | c0010 | t0001 | g0034 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0270 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0120 | AFR | LWK | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | LWK | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19043 | hp2 | a0014 | c0024 | t0001 | g0223 | AFR | LWK | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19085 | hp2 | a0015 | c0016 | t0001 | g0050 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19087 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19090 | hp2 | a0002 | c0011 | t0001 | g0057 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19240 | hp1 | a0003 | c0005 | t0001 | g0085 | AFR | YRI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | YRI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ASW | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ASW | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0226 | EUR | TSI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0058 | EUR | TSI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0053 | EUR | TSI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0248 | EUR | TSI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA20905 | hp1 | a0003 | c0003 | t0007 | g0286 | SAS | GIH | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | GIH | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02109 | hp1 | a0003 | c0009 | t0001 | g0041 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02486 | hp1 | a0005 | c0027 | t0001 | g0246 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02486 | hp2 | a0003 | c0015 | t0008 | g0287 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG02559 | hp2 | a0004 | c0006 | t0001 | g0275 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03471 | hp1 | a0003 | c0023 | t0001 | g0043 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG03471 | hp2 | a0004 | c0006 | t0001 | g0032 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | USA | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | USA | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | USA | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0009 | REF | REF | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0004 | REF | REF | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:154889392 | A | C | 1 | a0012 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.4288T>G | p.Ser1430Ala | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/28 | 4366/5404 | 4288/4527 | 1430/1508 | chr5 | 154889392 | |||
| chr5:154891455 | C | T | 1 | a0012 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.4048G>A | p.Glu1350Lys | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/28 | 4126/5404 | 4048/4527 | 1350/1508 | chr5 | 154891455 | |||
| chr5:154891677 | A | C | 1 | a0007 | 2 | HG02647.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.3826T>G | p.Leu1276Val | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/28 | 3904/5404 | 3826/4527 | 1276/1508 | chr5 | 154891677 | |||
| chr5:154896226 | G | A | 6 | a0002 a0005 a0007 others(3): Show |
45 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(42): Show |
missense_variant | MODERATE | c.3463C>T | p.Pro1155Ser | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/28 | 3541/5404 | 3463/4527 | 1155/1508 | chr5 | 154896226 | |||
| chr5:154896226 | G | C | 1 | a0005 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.3463C>G | p.Pro1155Ala | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/28 | 3541/5404 | 3463/4527 | 1155/1508 | chr5 | 154896226 | |||
| chr5:154896231 | T | G | 1 | a0010 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.3458A>C | p.Glu1153Ala | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/28 | 3536/5404 | 3458/4527 | 1153/1508 | chr5 | 154896231 | |||
| chr5:154896280 | A | G | 1 | a0011 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.3409T>C | p.Ser1137Pro | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/28 | 3487/5404 | 3409/4527 | 1137/1508 | chr5 | 154896280 | |||
| chr5:154898553 | C | T | 1 | a0014 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.3232G>A | p.Val1078Ile | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/28 | 3310/5404 | 3232/4527 | 1078/1508 | chr5 | 154898553 | |||
| chr5:154911849 | C | T | 8 | a0001 a0004 a0005 others(5): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
missense_variant | MODERATE | c.2045G>A | p.Arg682Gln | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/28 | 2123/5404 | 2045/4527 | 682/1508 | chr5 | 154911849 | |||
| chr5:154917961 | C | T | 1 | a0015 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1643G>A | p.Gly548Asp | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/28 | 1721/5404 | 1643/4527 | 548/1508 | chr5 | 154917961 | |||
| chr5:154921417 | T | G | 1 | a0004 | 6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
missense_variant | MODERATE | c.1388A>C | p.Gln463Pro | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/28 | 1466/5404 | 1388/4527 | 463/1508 | chr5 | 154921417 | |||
| chr5:154927510 | G | C | 1 | a0006 | 2 | HG02280.hp2 HG02698.hp2 |
missense_variant | MODERATE | c.955C>G | p.Arg319Gly | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/28 | 1033/5404 | 955/4527 | 319/1508 | chr5 | 154927510 | |||
| chr5:154931520 | C | G | 1 | a0013 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.719G>C | p.Cys240Ser | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/28 | 797/5404 | 719/4527 | 240/1508 | chr5 | 154931520 | |||
| chr5:154931560 | T | C | 1 | a0009 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.679A>G | p.Asn227Asp | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/28 | 757/5404 | 679/4527 | 227/1508 | chr5 | 154931560 | |||
| chr5:154937111 | G | A | 1 | a0004 | 6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
missense_variant | MODERATE | c.241C>T | p.Leu81Phe | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/28 | 319/5404 | 241/4527 | 81/1508 | chr5 | 154937111 | |||
| chr5:154937976 | G | T | 1 | a0008 | 2 | NA18954.hp2 NA19001.hp2 |
missense_variant | MODERATE | c.158C>A | p.Pro53Gln | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/28 | 236/5404 | 158/4527 | 53/1508 | chr5 | 154937976 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:154888336 | C | G | 1 | a0001c0025 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.4401G>C | p.Leu1467Leu | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 4479/5404 | 4401/4527 | 1467/1508 | chr5 | 154888336 | |||
| chr5:154889342 | C | T | 27 | a0001c0001 a0001c0004 a0001c0014 others(24): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
synonymous_variant | LOW | c.4338G>A | p.Ala1446Ala | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/28 | 4416/5404 | 4338/4527 | 1446/1508 | chr5 | 154889342 | |||
| chr5:154891327 | T | C | 1 | a0003c0005 | 7 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(4): Show |
synonymous_variant | LOW | c.4176A>G | p.Gln1392Gln | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/28 | 4254/5404 | 4176/4527 | 1392/1508 | chr5 | 154891327 | |||
| chr5:154892388 | G | A | 27 | a0001c0001 a0001c0004 a0001c0014 others(24): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
splice_region_variant&synonymous_variant | LOW | c.3759C>T | p.Asp1253Asp | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/28 | 3837/5404 | 3759/4527 | 1253/1508 | chr5 | 154892388 | |||
| chr5:154892457 | C | A | 1 | a0002c0011 | 2 | HG03831.hp1 NA19090.hp2 |
synonymous_variant | LOW | c.3690G>T | p.Ala1230Ala | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/28 | 3768/5404 | 3690/4527 | 1230/1508 | chr5 | 154892457 | |||
| chr5:154896122 | T | C | 1 | a0002c0021 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.3567A>G | p.Pro1189Pro | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/28 | 3645/5404 | 3567/4527 | 1189/1508 | chr5 | 154896122 | |||
| chr5:154899193 | T | C | 1 | a0001c0029 | 1 | HG01934.hp1 | splice_region_variant&synonymous_variant | LOW | c.3132A>G | p.Lys1044Lys | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 22/28 | 3210/5404 | 3132/4527 | 1044/1508 | chr5 | 154899193 | |||
| chr5:154899274 | C | T | 1 | a0002c0018 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.3051G>A | p.Pro1017Pro | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 22/28 | 3129/5404 | 3051/4527 | 1017/1508 | chr5 | 154899274 | |||
| chr5:154902567 | T | C | 1 | a0007c0022 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.2838A>G | p.Thr946Thr | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/28 | 2916/5404 | 2838/4527 | 946/1508 | chr5 | 154902567 | |||
| chr5:154902603 | A | G | 1 | a0002c0008 | 3 | HG01243.hp1 HG02055.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.2802T>C | p.Gly934Gly | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/28 | 2880/5404 | 2802/4527 | 934/1508 | chr5 | 154902603 | |||
| chr5:154902675 | T | C | 12 | a0002c0002 a0002c0008 a0002c0011 others(9): Show |
48 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(45): Show |
splice_region_variant&synonymous_variant | LOW | c.2730A>G | p.Gly910Gly | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/28 | 2808/5404 | 2730/4527 | 910/1508 | chr5 | 154902675 | |||
| chr5:154904511 | G | A | 1 | a0003c0023 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2628C>T | p.Ser876Ser | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/28 | 2706/5404 | 2628/4527 | 876/1508 | chr5 | 154904511 | |||
| chr5:154911854 | T | C | 1 | a0001c0030 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.2040A>G | p.Gly680Gly | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/28 | 2118/5404 | 2040/4527 | 680/1508 | chr5 | 154911854 | |||
| chr5:154921353 | G | T | 1 | a0003c0015 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1452C>A | p.Pro484Pro | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/28 | 1530/5404 | 1452/4527 | 484/1508 | chr5 | 154921353 | |||
| chr5:154921380 | A | C | 12 | a0001c0001 a0001c0014 a0001c0025 others(9): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
synonymous_variant | LOW | c.1425T>G | p.Thr475Thr | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/28 | 1503/5404 | 1425/4527 | 475/1508 | chr5 | 154921380 | |||
| chr5:154927412 | T | C | 13 | a0001c0001 a0001c0004 a0001c0025 others(10): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
synonymous_variant | LOW | c.1053A>G | p.Leu351Leu | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/28 | 1131/5404 | 1053/4527 | 351/1508 | chr5 | 154927412 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:154887481 | G | A | 1 | a0001c0004t0005 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*729C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 729 | chr5 | 154887481 | ||||||
| chr5:154887487 | T | C | 1 | a0001c0001t0003 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*723A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 723 | chr5 | 154887487 | ||||||
| chr5:154887540 | T | A | 1 | a0012c0017t0004 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*670A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 670 | chr5 | 154887540 | ||||||
| chr5:154887577 | T | A | 1 | a0001c0004t0005 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*633A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 633 | chr5 | 154887577 | ||||||
| chr5:154887718 | T | C | 1 | a0001c0001t0006 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*492A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 492 | chr5 | 154887718 | ||||||
| chr5:154887728 | A | G | 5 | a0001c0001t0002 a0001c0001t0003 a0001c0029t0002 others(2): Show |
42 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*482T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 482 | chr5 | 154887728 | ||||||
| chr5:154938191 | G | C | 1 | a0003c0003t0007 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/28 | 58 | chr5 | 154938191 | ||||||
| chr5:154938194 | T | G | 1 | a0003c0015t0008 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/28 | 61 | chr5 | 154938194 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:154888648 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4360-271G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154888648 | |||||||
| chr5:154888855 | T | TTTTTG | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(274): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.4359+461_4359+465d others(7): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154888855 | |||||||
| chr5:154888900 | C | T | 5 | a0004c0006t0001g0032 a0004c0006t0001g0273 a0004c0006t0001g0274 others(2): Show |
6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.4359+421G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154888900 | |||||||
| chr5:154888919 | G | A | 8 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0137 others(5): Show |
8 | HG00558.hp1 HG00621.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.4359+402C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154888919 | |||||||
| chr5:154888985 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4359+336A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154888985 | |||||||
| chr5:154889066 | C | T | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4359+255G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154889066 | |||||||
| chr5:154889106 | G | A | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4359+215C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154889106 | |||||||
| chr5:154889143 | T | A | 44 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(41): Show |
49 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.4359+178A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154889143 | |||||||
| chr5:154889505 | T | C | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4263-88A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154889505 | |||||||
| chr5:154889545 | T | C | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4263-128A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154889545 | |||||||
| chr5:154889706 | G | T | 1 | a0001c0001t0001g0258 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4263-289C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154889706 | |||||||
| chr5:154889784 | T | C | 1 | a0001c0001t0002g0228 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4263-367A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154889784 | |||||||
| chr5:154889809 | C | T | 1 | a0002c0002t0001g0067 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.4263-392G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154889809 | |||||||
| chr5:154890054 | C | T | 8 | a0001c0004t0001g0119 a0001c0004t0001g0120 a0001c0004t0001g0121 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.4263-637G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890054 | |||||||
| chr5:154890087 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.4263-670A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890087 | |||||||
| chr5:154890254 | T | G | 1 | a0003c0007t0001g0072 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4263-837A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890254 | |||||||
| chr5:154890269 | T | A | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4263-852A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890269 | |||||||
| chr5:154890459 | A | G | 36 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(33): Show |
41 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.4262+782T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890459 | |||||||
| chr5:154890467 | A | AT | 14 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0001t0001g0153 others(11): Show |
14 | HG00140.hp2 HG02148.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.4262+773dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890467 | |||||||
| chr5:154890467 | AT | A | 11 | a0001c0001t0001g0096 a0001c0001t0001g0135 a0001c0001t0001g0170 others(8): Show |
11 | HG00735.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.4262+773delA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890467 | |||||||
| chr5:154890614 | C | T | 2 | a0007c0020t0001g0065 a0007c0022t0001g0049 |
2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4262+627G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890614 | |||||||
| chr5:154890936 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(263): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.4262+305T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890936 | |||||||
| chr5:154891004 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4262+237G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154891004 | |||||||
| chr5:154891035 | C | T | 2 | a0003c0005t0001g0077 a0003c0005t0001g0079 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.4262+206G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154891035 | |||||||
| chr5:154891051 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0160 a0001c0001t0001g0176 |
6 | HG01106.hp1 HG01123.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.4262+190G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154891051 | |||||||
| chr5:154891055 | C | CT | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(174): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.4262+185dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154891055 | |||||||
| chr5:154891055 | C | CTT | 78 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0098 others(75): Show |
85 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.4262+184_4262+185d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154891055 | |||||||
| chr5:154891055 | C | CTTT | 12 | a0001c0004t0001g0125 a0002c0002t0001g0037 a0002c0002t0001g0047 others(9): Show |
12 | HG01109.hp1 HG01346.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.4262+183_4262+185d others(5): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154891055 | |||||||
| chr5:154891786 | T | C | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3761-44A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/27 | chr5 | 154891786 | |||||||
| chr5:154891831 | A | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.3761-89T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/27 | chr5 | 154891831 | |||||||
| chr5:154891977 | T | C | 36 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(33): Show |
41 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.3761-235A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/27 | chr5 | 154891977 | |||||||
| chr5:154892035 | C | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0130 a0001c0001t0001g0134 others(4): Show |
9 | HG00609.hp1 HG02129.hp2 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.3761-293G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/27 | chr5 | 154892035 | |||||||
| chr5:154892072 | A | C | 1 | a0003c0003t0001g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3760+315T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/27 | chr5 | 154892072 | |||||||
| chr5:154892240 | C | T | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3760+147G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/27 | chr5 | 154892240 | |||||||
| chr5:154892631 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3598-82C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892631 | |||||||
| chr5:154892706 | A | G | 1 | a0009c0031t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3598-157T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892706 | |||||||
| chr5:154892776 | G | A | 2 | a0003c0007t0001g0044 a0003c0007t0001g0045 |
2 | HG02080.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.3598-227C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892776 | |||||||
| chr5:154892902 | G | T | 2 | a0003c0009t0001g0040 a0003c0009t0001g0041 |
2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3598-353C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892902 | |||||||
| chr5:154892925 | C | T | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3598-376G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892925 | |||||||
| chr5:154892926 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3598-377C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892926 | |||||||
| chr5:154892927 | C | T | 3 | a0001c0001t0001g0130 a0001c0004t0005g0039 a0012c0017t0004g0279 |
3 | HG02630.hp2 HG03453.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3598-378G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892927 | |||||||
| chr5:154893037 | T | C | 51 | a0001c0004t0005g0039 a0002c0002t0001g0007 a0002c0002t0001g0011 others(48): Show |
56 | HG00558.hp2 HG00597.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.3598-488A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893037 | |||||||
| chr5:154893054 | G | A | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3598-505C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893054 | |||||||
| chr5:154893097 | A | AAAAC | 43 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(40): Show |
48 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.3598-552_3598-549d others(6): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893097 | |||||||
| chr5:154893105 | C | A | 2 | a0003c0003t0001g0088 a0003c0003t0001g0089 |
2 | HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3598-556G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893105 | |||||||
| chr5:154893224 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3598-675C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893224 | |||||||
| chr5:154893249 | C | T | 8 | a0003c0003t0001g0035 a0003c0015t0008g0287 a0004c0006t0001g0032 others(5): Show |
9 | HG02486.hp2 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3598-700G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893249 | |||||||
| chr5:154893255 | T | TA | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(161): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.3598-707dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893255 | |||||||
| chr5:154893255 | T | TAA | 51 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0023 others(48): Show |
54 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.3598-708_3598-707d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893255 | |||||||
| chr5:154893255 | TAAAAAAA others(10): Show |
T | 5 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | NA19006.hp1 NA19011.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.3598-723_3598-707d others(19): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893255 | |||||||
| chr5:154893329 | C | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(59): Show |
75 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.3598-780G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893329 | |||||||
| chr5:154893335 | C | T | 1 | a0002c0002t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3598-786G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893335 | |||||||
| chr5:154893343 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0152 a0001c0001t0001g0167 |
3 | HG00423.hp1 NA18968.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.3598-794A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893343 | |||||||
| chr5:154893387 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(143): Show |
174 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.3598-838G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893387 | |||||||
| chr5:154893388 | G | A | 3 | a0001c0001t0002g0225 a0001c0001t0002g0234 a0001c0001t0002g0235 |
3 | HG01168.hp1 HG01175.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3598-839C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893388 | |||||||
| chr5:154893410 | C | T | 1 | a0002c0002t0001g0074 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3598-861G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893410 | |||||||
| chr5:154893418 | C | CA | 8 | a0001c0001t0001g0200 a0001c0001t0001g0204 a0001c0001t0001g0259 others(5): Show |
8 | HG00438.hp1 HG01109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3598-870dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893418 | |||||||
| chr5:154893517 | CAT | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG01070.hp1 HG01934.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3598-970_3598-969d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893517 | |||||||
| chr5:154893600 | C | T | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3598-1051G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893600 | |||||||
| chr5:154893813 | G | A | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3598-1264C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893813 | |||||||
| chr5:154893893 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3598-1344C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893893 | |||||||
| chr5:154893903 | G | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(263): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.3598-1354C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893903 | |||||||
| chr5:154894141 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.3598-1592A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894141 | |||||||
| chr5:154894210 | G | A | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3598-1661C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894210 | |||||||
| chr5:154894421 | G | A | 3 | a0002c0008t0001g0062 a0002c0008t0001g0063 a0002c0008t0001g0064 |
3 | HG01243.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3597+1671C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894421 | |||||||
| chr5:154894519 | A | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.3597+1573T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894519 | |||||||
| chr5:154894797 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3597+1295G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894797 | |||||||
| chr5:154894881 | C | T | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3597+1211G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894881 | |||||||
| chr5:154894905 | T | TA | 12 | a0001c0004t0001g0120 a0001c0004t0001g0121 a0001c0004t0001g0122 others(9): Show |
13 | HG02257.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.3597+1186dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894905 | |||||||
| chr5:154894939 | C | T | 1 | a0002c0018t0001g0046 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3597+1153G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894939 | |||||||
| chr5:154895003 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3597+1089A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895003 | |||||||
| chr5:154895004 | G | A | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3597+1088C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895004 | |||||||
| chr5:154895045 | C | CCTTGTTG others(9): Show |
37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.3597+1046_3597+104 others(20): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895045 | |||||||
| chr5:154895047 | C | G | 37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.3597+1045G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895047 | |||||||
| chr5:154895048 | C | T | 37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.3597+1044G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895048 | |||||||
| chr5:154895049 | A | T | 37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.3597+1043T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895049 | |||||||
| chr5:154895098 | A | C | 1 | a0001c0001t0002g0242 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3597+994T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895098 | |||||||
| chr5:154895132 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.3597+960A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895132 | |||||||
| chr5:154895188 | G | C | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3597+904C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895188 | |||||||
| chr5:154895335 | G | GGA | 42 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(39): Show |
47 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.3597+755_3597+756d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895335 | |||||||
| chr5:154895336 | GAAAA | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0097 others(8): Show |
15 | HG00140.hp2 HG00642.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3597+752_3597+755d others(6): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895336 | |||||||
| chr5:154895360 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3597+732C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895360 | |||||||
| chr5:154895521 | T | G | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3597+571A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895521 | |||||||
| chr5:154895570 | T | G | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3597+522A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895570 | |||||||
| chr5:154895674 | TATTAC | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3597+413_3597+417d others(7): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895674 | |||||||
| chr5:154895757 | C | T | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3597+335G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895757 | |||||||
| chr5:154895762 | G | A | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3597+330C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895762 | |||||||
| chr5:154895785 | G | A | 13 | a0001c0004t0001g0119 a0001c0004t0001g0120 a0001c0004t0001g0121 others(10): Show |
14 | HG02257.hp2 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.3597+307C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895785 | |||||||
| chr5:154895937 | T | C | 13 | a0001c0004t0001g0119 a0001c0004t0001g0120 a0001c0004t0001g0121 others(10): Show |
14 | HG02257.hp2 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.3597+155A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895937 | |||||||
| chr5:154896019 | G | A | 4 | a0001c0001t0002g0029 a0001c0001t0002g0241 a0001c0001t0003g0244 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3597+73C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154896019 | |||||||
| chr5:154896402 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(144): Show |
175 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.3346-59C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154896402 | |||||||
| chr5:154896451 | C | A | 32 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(29): Show |
37 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.3346-108G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154896451 | |||||||
| chr5:154896470 | T | C | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3346-127A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154896470 | |||||||
| chr5:154896501 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(265): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.3346-158T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154896501 | |||||||
| chr5:154896868 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3346-525G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154896868 | |||||||
| chr5:154897113 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.3346-770A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897113 | |||||||
| chr5:154897177 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.3346-834T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897177 | |||||||
| chr5:154897403 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3345+1037C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897403 | |||||||
| chr5:154897440 | C | G | 3 | a0002c0008t0001g0062 a0002c0008t0001g0063 a0002c0008t0001g0064 |
3 | HG01243.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3345+1000G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897440 | |||||||
| chr5:154897465 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.3345+975T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897465 | |||||||
| chr5:154897724 | C | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(275): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.3345+716G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897724 | |||||||
| chr5:154897745 | G | GT | 7 | a0001c0001t0001g0147 a0001c0001t0001g0251 a0004c0006t0001g0032 others(4): Show |
8 | HG01981.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.3345+694dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897745 | |||||||
| chr5:154897902 | GT | G | 8 | a0001c0004t0001g0119 a0001c0004t0001g0120 a0001c0004t0001g0121 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.3345+537delA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897902 | |||||||
| chr5:154897903 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3345+537A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897903 | |||||||
| chr5:154897913 | T | TG | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3345+526dupC | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897913 | |||||||
| chr5:154897914 | G | GT | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(135): Show |
169 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.3345+525dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897914 | |||||||
| chr5:154897914 | G | GTT | 69 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0106 others(66): Show |
77 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.3345+524_3345+525d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897914 | |||||||
| chr5:154897979 | A | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.3345+461T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897979 | |||||||
| chr5:154897985 | C | T | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3345+455G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897985 | |||||||
| chr5:154898076 | T | G | 3 | a0001c0001t0001g0190 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG00609.hp2 HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.3345+364A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154898076 | |||||||
| chr5:154898127 | C | T | 9 | a0003c0003t0001g0088 a0003c0003t0001g0089 a0003c0005t0001g0077 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3345+313G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154898127 | |||||||
| chr5:154898386 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0169 a0001c0001t0001g0171 |
4 | HG01167.hp1 HG01169.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+54T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154898386 | |||||||
| chr5:154898786 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3135-136A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 22/27 | chr5 | 154898786 | |||||||
| chr5:154898934 | A | G | 2 | a0001c0001t0002g0247 a0001c0001t0002g0248 |
2 | HG01099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3134+257T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 22/27 | chr5 | 154898934 | |||||||
| chr5:154899328 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.3015-18G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899328 | |||||||
| chr5:154899572 | A | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3015-262T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899572 | |||||||
| chr5:154899619 | TA | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(257): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.3015-310delT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899619 | |||||||
| chr5:154899621 | A | T | 1 | a0002c0002t0001g0007 | 3 | HG02280.hp1 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3015-311T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899621 | |||||||
| chr5:154899829 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3015-519A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899829 | |||||||
| chr5:154899931 | T | TA | 9 | a0001c0001t0001g0171 a0001c0004t0005g0039 a0002c0002t0001g0052 others(6): Show |
9 | HG00558.hp2 HG01109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.3015-622dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899931 | |||||||
| chr5:154899983 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3015-673A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899983 | |||||||
| chr5:154900138 | A | G | 32 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(29): Show |
37 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.3015-828T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900138 | |||||||
| chr5:154900217 | T | C | 1 | a0003c0005t0001g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3015-907A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900217 | |||||||
| chr5:154900252 | A | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3015-942T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900252 | |||||||
| chr5:154900436 | A | T | 1 | a0001c0001t0001g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3014+903T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900436 | |||||||
| chr5:154900454 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3014+885C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900454 | |||||||
| chr5:154900839 | T | G | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3014+500A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900839 | |||||||
| chr5:154900844 | G | T | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3014+495C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900844 | |||||||
| chr5:154900885 | G | GTCCAAAC | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.3014+453_3014+454i others(9): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900885 | |||||||
| chr5:154900949 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3014+390G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900949 | |||||||
| chr5:154901162 | C | T | 6 | a0001c0004t0001g0119 a0001c0004t0001g0120 a0001c0004t0001g0121 others(3): Show |
6 | HG02257.hp2 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014+177G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154901162 | |||||||
| chr5:154901163 | A | G | 5 | a0002c0002t0001g0055 a0002c0002t0001g0058 a0002c0002t0001g0059 others(2): Show |
5 | HG01081.hp1 HG01123.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3014+176T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154901163 | |||||||
| chr5:154901508 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0189 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2867-22C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901508 | |||||||
| chr5:154901656 | G | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(269): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.2867-170C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901656 | |||||||
| chr5:154901676 | T | G | 1 | a0001c0001t0001g0030 | 2 | NA18612.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.2867-190A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901676 | |||||||
| chr5:154901744 | A | G | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2867-258T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901744 | |||||||
| chr5:154901795 | T | TTC | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(246): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.2867-310_2867-309i others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901795 | |||||||
| chr5:154901795 | T | TTTC | 18 | a0001c0001t0001g0020 a0001c0001t0001g0096 a0001c0001t0001g0169 others(15): Show |
20 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.2867-310_2867-309i others(5): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901795 | |||||||
| chr5:154901853 | G | A | 42 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(39): Show |
47 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.2867-367C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901853 | |||||||
| chr5:154901856 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0022 others(40): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.2867-370C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901856 | |||||||
| chr5:154901894 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2867-408C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901894 | |||||||
| chr5:154901948 | A | G | 1 | a0003c0023t0001g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2867-462T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901948 | |||||||
| chr5:154902274 | A | G | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2866+265T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154902274 | |||||||
| chr5:154902378 | G | T | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2866+161C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154902378 | |||||||
| chr5:154902384 | G | A | 1 | a0001c0025t0001g0178 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2866+155C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154902384 | |||||||
| chr5:154902683 | G | C | 37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
splice_region_variant&intron_variant | LOW | c.2729-7C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 19/27 | chr5 | 154902683 | |||||||
| chr5:154902847 | C | A | 37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.2729-171G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 19/27 | chr5 | 154902847 | |||||||
| chr5:154902991 | T | C | 53 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0097 others(50): Show |
63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2728+89A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 19/27 | chr5 | 154902991 | |||||||
| chr5:154903279 | A | C | 8 | a0001c0004t0001g0119 a0001c0004t0001g0120 a0001c0004t0001g0121 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2633-104T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903279 | |||||||
| chr5:154903515 | G | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0111 others(8): Show |
13 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2633-340C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903515 | |||||||
| chr5:154903540 | T | G | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2633-365A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903540 | |||||||
| chr5:154903636 | A | G | 3 | a0002c0008t0001g0062 a0002c0008t0001g0063 a0002c0008t0001g0064 |
3 | HG01243.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2633-461T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903636 | |||||||
| chr5:154903637 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2633-462A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903637 | |||||||
| chr5:154903671 | T | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2633-496A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903671 | |||||||
| chr5:154903810 | C | T | 1 | a0003c0009t0001g0042 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2633-635G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903810 | |||||||
| chr5:154903826 | A | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0153 |
2 | NA18971.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2633-651T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903826 | |||||||
| chr5:154903834 | A | T | 2 | a0001c0001t0001g0170 a0001c0001t0002g0227 |
2 | HG00735.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2633-659T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903834 | |||||||
| chr5:154903835 | T | A | 32 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(29): Show |
37 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.2633-660A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903835 | |||||||
| chr5:154903846 | A | T | 1 | a0001c0001t0002g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2632+661T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903846 | |||||||
| chr5:154904092 | A | T | 3 | a0003c0009t0001g0040 a0003c0009t0001g0041 a0003c0009t0001g0042 |
3 | HG02109.hp1 HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2632+415T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154904092 | |||||||
| chr5:154904100 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.2632+407G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154904100 | |||||||
| chr5:154904104 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.2632+403T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154904104 | |||||||
| chr5:154904146 | AT | A | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2632+360delA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154904146 | |||||||
| chr5:154904756 | A | G | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2510-127T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154904756 | |||||||
| chr5:154904822 | T | C | 1 | a0001c0004t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2510-193A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154904822 | |||||||
| chr5:154904964 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2510-335C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154904964 | |||||||
| chr5:154905086 | C | T | 1 | a0011c0019t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2509+277G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154905086 | |||||||
| chr5:154905143 | A | C | 1 | a0001c0001t0001g0262 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2509+220T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154905143 | |||||||
| chr5:154905143 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2509+220T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154905143 | |||||||
| chr5:154905259 | A | C | 1 | a0003c0023t0001g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2509+104T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154905259 | |||||||
| chr5:154905557 | C | A | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2396-81G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905557 | |||||||
| chr5:154905609 | A | G | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2396-133T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905609 | |||||||
| chr5:154905634 | G | A | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2396-158C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905634 | |||||||
| chr5:154905700 | G | GT | 57 | a0001c0001t0001g0024 a0001c0001t0001g0098 a0001c0001t0001g0112 others(54): Show |
63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.2396-225dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905700 | |||||||
| chr5:154905700 | G | GTT | 8 | a0002c0002t0001g0047 a0002c0002t0001g0055 a0002c0002t0001g0068 others(5): Show |
8 | HG01123.hp1 HG01975.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2396-226_2396-225d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905700 | |||||||
| chr5:154905700 | G | T | 10 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0137 others(7): Show |
10 | HG00558.hp1 HG00621.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2396-224C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905700 | |||||||
| chr5:154905760 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2396-284G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905760 | |||||||
| chr5:154905959 | G | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0102 a0001c0001t0001g0104 others(15): Show |
20 | HG00323.hp2 HG00609.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.2396-483C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905959 | |||||||
| chr5:154906196 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0265 |
3 | HG03017.hp1 HG03491.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2396-720T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154906196 | |||||||
| chr5:154906208 | C | T | 41 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(38): Show |
47 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.2396-732G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154906208 | |||||||
| chr5:154906246 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.2396-770A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154906246 | |||||||
| chr5:154906271 | C | T | 2 | a0003c0005t0001g0085 a0003c0005t0001g0087 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2396-795G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154906271 | |||||||
| chr5:154906425 | C | T | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2396-949G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154906425 | |||||||
| chr5:154907078 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.2395+513G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907078 | |||||||
| chr5:154907194 | G | C | 1 | a0001c0001t0002g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2395+397C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907194 | |||||||
| chr5:154907243 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2395+348G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907243 | |||||||
| chr5:154907309 | A | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.2395+282T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907309 | |||||||
| chr5:154907330 | C | T | 17 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0106 others(14): Show |
19 | HG00423.hp1 HG02071.hp2 NA18747.hp2 others(16): Show |
intron_variant | MODIFIER | c.2395+261G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907330 | |||||||
| chr5:154907424 | A | G | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2395+167T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907424 | |||||||
| chr5:154907456 | T | TGAAAAAA others(1): Show |
13 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(10): Show |
15 | HG00609.hp1 HG02056.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.2395+134_2395+135i others(10): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907456 | |||||||
| chr5:154907456 | T | TGAAAAAA others(2): Show |
250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.2395+134_2395+135i others(11): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907456 | |||||||
| chr5:154907456 | T | TGAAAAAA others(3): Show |
4 | a0001c0001t0001g0146 a0001c0001t0002g0226 a0003c0007t0001g0072 others(1): Show |
4 | HG02486.hp2 NA18940.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.2395+134_2395+135i others(12): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907456 | |||||||
| chr5:154907555 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.2395+36A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907555 | |||||||
| chr5:154907835 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2168-17T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154907835 | |||||||
| chr5:154907880 | T | C | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2168-62A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154907880 | |||||||
| chr5:154907900 | T | C | 1 | a0002c0018t0001g0046 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2168-82A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154907900 | |||||||
| chr5:154908038 | G | C | 1 | a0001c0001t0001g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2168-220C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908038 | |||||||
| chr5:154908170 | TC | T | 5 | a0002c0008t0001g0064 a0002c0018t0001g0046 a0007c0020t0001g0065 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2168-353delG | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908170 | |||||||
| chr5:154908171 | C | CT | 5 | a0002c0002t0001g0011 a0002c0002t0001g0047 a0003c0009t0001g0040 others(2): Show |
5 | HG01255.hp2 HG02109.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2168-354_2168-353i others(3): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908171 | |||||||
| chr5:154908172 | C | CT | 40 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0021 others(37): Show |
48 | HG00140.hp2 HG00323.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.2168-355dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908172 | |||||||
| chr5:154908172 | C | CTT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(104): Show |
132 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.2168-356_2168-355d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908172 | |||||||
| chr5:154908172 | C | CTTT | 29 | a0001c0001t0001g0026 a0001c0001t0001g0094 a0001c0001t0001g0106 others(26): Show |
30 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.2168-357_2168-355d others(5): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908172 | |||||||
| chr5:154908172 | C | T | 38 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(35): Show |
43 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.2168-354G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908172 | |||||||
| chr5:154908212 | C | T | 2 | a0001c0014t0001g0209 a0002c0002t0001g0066 |
2 | HG00621.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2168-394G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908212 | |||||||
| chr5:154908328 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2168-510C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908328 | |||||||
| chr5:154908337 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2168-519G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908337 | |||||||
| chr5:154908369 | C | T | 1 | a0011c0019t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2168-551G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908369 | |||||||
| chr5:154908418 | T | A | 1 | a0001c0014t0001g0209 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2168-600A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908418 | |||||||
| chr5:154908472 | C | T | 1 | a0003c0009t0001g0041 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2168-654G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908472 | |||||||
| chr5:154908608 | C | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(275): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.2168-790G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908608 | |||||||
| chr5:154908654 | T | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0096 a0001c0001t0001g0169 others(4): Show |
8 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.2168-836A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908654 | |||||||
| chr5:154908866 | G | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2168-1048C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908866 | |||||||
| chr5:154908888 | G | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0174 |
3 | HG01981.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2168-1070C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908888 | |||||||
| chr5:154909019 | A | G | 8 | a0001c0004t0001g0119 a0001c0004t0001g0120 a0001c0004t0001g0121 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2168-1201T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909019 | |||||||
| chr5:154909055 | C | T | 5 | a0004c0006t0001g0032 a0004c0006t0001g0273 a0004c0006t0001g0274 others(2): Show |
6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2168-1237G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909055 | |||||||
| chr5:154909107 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2168-1289G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909107 | |||||||
| chr5:154909133 | A | AT | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(136): Show |
165 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.2168-1316dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909133 | |||||||
| chr5:154909133 | A | ATT | 63 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(60): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.2168-1317_2168-131 others(6): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909133 | |||||||
| chr5:154909133 | A | ATTT | 10 | a0001c0001t0001g0169 a0001c0001t0002g0224 a0001c0001t0002g0227 others(7): Show |
10 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.2168-1318_2168-131 others(7): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909133 | |||||||
| chr5:154909533 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(220): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2168-1715T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909533 | |||||||
| chr5:154909553 | TACC | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2168-1738_2168-173 others(7): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909553 | |||||||
| chr5:154909620 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0111 others(8): Show |
13 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2168-1802G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909620 | |||||||
| chr5:154909701 | G | A | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2168-1883C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909701 | |||||||
| chr5:154909723 | A | G | 8 | a0001c0004t0001g0119 a0001c0004t0001g0120 a0001c0004t0001g0121 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2168-1905T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909723 | |||||||
| chr5:154909750 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2168-1932C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909750 | |||||||
| chr5:154909800 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2167+1927C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909800 | |||||||
| chr5:154909827 | A | G | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2167+1900T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909827 | |||||||
| chr5:154909849 | C | T | 5 | a0004c0006t0001g0032 a0004c0006t0001g0273 a0004c0006t0001g0274 others(2): Show |
6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2167+1878G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909849 | |||||||
| chr5:154909980 | AG | A | 4 | a0003c0009t0001g0040 a0003c0009t0001g0041 a0003c0009t0001g0042 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+1746delC | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909980 | |||||||
| chr5:154909981 | G | GA | 74 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(71): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.2167+1745dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909981 | |||||||
| chr5:154910005 | A | C | 1 | a0001c0025t0001g0178 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2167+1722T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910005 | |||||||
| chr5:154910193 | T | G | 37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.2167+1534A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910193 | |||||||
| chr5:154910290 | T | G | 1 | a0001c0029t0002g0277 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2167+1437A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910290 | |||||||
| chr5:154910303 | T | C | 8 | a0001c0004t0001g0119 a0001c0004t0001g0120 a0001c0004t0001g0121 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2167+1424A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910303 | |||||||
| chr5:154910313 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2167+1414A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910313 | |||||||
| chr5:154910323 | A | C | 32 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(29): Show |
37 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.2167+1404T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910323 | |||||||
| chr5:154910356 | G | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2167+1371C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910356 | |||||||
| chr5:154910402 | C | T | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2167+1325G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910402 | |||||||
| chr5:154910479 | G | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.2167+1248C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910479 | |||||||
| chr5:154910531 | T | C | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2167+1196A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910531 | |||||||
| chr5:154910624 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2167+1103A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910624 | |||||||
| chr5:154910763 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2167+964T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910763 | |||||||
| chr5:154910794 | C | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2167+933G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910794 | |||||||
| chr5:154910878 | T | G | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2167+849A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910878 | |||||||
| chr5:154910912 | T | G | 4 | a0003c0009t0001g0040 a0003c0009t0001g0041 a0003c0009t0001g0042 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+815A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910912 | |||||||
| chr5:154910997 | C | T | 5 | a0002c0018t0001g0046 a0003c0009t0001g0040 a0003c0009t0001g0041 others(2): Show |
5 | HG01109.hp1 HG02109.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2167+730G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910997 | |||||||
| chr5:154911032 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2167+695A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911032 | |||||||
| chr5:154911101 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2167+626A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911101 | |||||||
| chr5:154911117 | A | G | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2167+610T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911117 | |||||||
| chr5:154911144 | C | T | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2167+583G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911144 | |||||||
| chr5:154911191 | G | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(143): Show |
174 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.2167+536C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911191 | |||||||
| chr5:154911232 | G | A | 1 | a0001c0001t0002g0248 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2167+495C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911232 | |||||||
| chr5:154911241 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2167+486G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911241 | |||||||
| chr5:154911242 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2167+485C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911242 | |||||||
| chr5:154911375 | T | C | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2167+352A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911375 | |||||||
| chr5:154911418 | T | C | 2 | a0003c0005t0001g0085 a0003c0005t0001g0087 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2167+309A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911418 | |||||||
| chr5:154911421 | G | A | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2167+306C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911421 | |||||||
| chr5:154911456 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.2167+271G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911456 | |||||||
| chr5:154911460 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2167+267G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911460 | |||||||
| chr5:154911659 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2167+68T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911659 | |||||||
| chr5:154911936 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1996-38C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154911936 | |||||||
| chr5:154912167 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1996-269G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912167 | |||||||
| chr5:154912410 | C | T | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1995+489G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912410 | |||||||
| chr5:154912490 | T | G | 1 | a0003c0023t0001g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1995+409A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912490 | |||||||
| chr5:154912530 | C | T | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1995+369G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912530 | |||||||
| chr5:154912533 | T | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1995+366A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912533 | |||||||
| chr5:154912706 | CA | C | 49 | a0001c0004t0005g0039 a0002c0002t0001g0007 a0002c0002t0001g0011 others(46): Show |
54 | HG00558.hp2 HG00597.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.1995+192delT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912706 | |||||||
| chr5:154912727 | A | G | 1 | a0001c0001t0002g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1995+172T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912727 | |||||||
| chr5:154912812 | G | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1995+87C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912812 | |||||||
| chr5:154913082 | C | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0166 |
3 | NA18939.hp1 NA18946.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1856-44G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913082 | |||||||
| chr5:154913171 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1856-133T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913171 | |||||||
| chr5:154913190 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1856-152A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913190 | |||||||
| chr5:154913437 | T | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(275): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1856-399A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913437 | |||||||
| chr5:154913627 | C | G | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1856-589G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913627 | |||||||
| chr5:154913682 | T | C | 1 | a0003c0003t0001g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1856-644A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913682 | |||||||
| chr5:154913873 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.1856-835A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913873 | |||||||
| chr5:154914014 | AATAC | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0186 others(5): Show |
9 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1856-980_1856-977d others(6): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914014 | |||||||
| chr5:154914202 | G | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(91): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1856-1164C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914202 | |||||||
| chr5:154914303 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1856-1265C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914303 | |||||||
| chr5:154914509 | CT | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(210): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1856-1472delA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914509 | |||||||
| chr5:154914509 | CTT | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0093 a0001c0001t0001g0168 others(7): Show |
11 | HG00408.hp2 HG01081.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1856-1473_1856-147 others(6): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914509 | |||||||
| chr5:154914598 | C | A | 1 | a0003c0007t0001g0073 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1856-1560G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914598 | |||||||
| chr5:154914904 | T | C | 1 | a0001c0001t0002g0249 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1856-1866A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914904 | |||||||
| chr5:154914946 | G | C | 1 | a0001c0001t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1856-1908C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914946 | |||||||
| chr5:154915103 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1855+1895G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915103 | |||||||
| chr5:154915256 | G | C | 2 | a0001c0001t0001g0215 a0001c0001t0006g0214 |
2 | HG04199.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1855+1742C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915256 | |||||||
| chr5:154915262 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1855+1736A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915262 | |||||||
| chr5:154915493 | T | C | 1 | a0002c0002t0001g0066 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1855+1505A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915493 | |||||||
| chr5:154915687 | G | A | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1855+1311C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915687 | |||||||
| chr5:154915735 | C | A | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1855+1263G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915735 | |||||||
| chr5:154915817 | A | C | 1 | a0002c0002t0001g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1855+1181T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915817 | |||||||
| chr5:154915861 | A | G | 1 | a0001c0001t0001g0022 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1855+1137T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915861 | |||||||
| chr5:154915894 | ATTAT | A | 37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1855+1100_1855+110 others(8): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915894 | |||||||
| chr5:154915912 | C | T | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1855+1086G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915912 | |||||||
| chr5:154916052 | T | A | 38 | a0001c0001t0002g0243 a0002c0002t0001g0007 a0002c0002t0001g0011 others(35): Show |
43 | HG00597.hp2 HG00741.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.1855+946A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916052 | |||||||
| chr5:154916230 | T | C | 5 | a0004c0006t0001g0032 a0004c0006t0001g0273 a0004c0006t0001g0274 others(2): Show |
6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1855+768A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916230 | |||||||
| chr5:154916271 | G | GA | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0105 others(9): Show |
14 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1855+726dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916271 | |||||||
| chr5:154916403 | T | C | 4 | a0001c0004t0001g0119 a0001c0004t0001g0122 a0001c0004t0001g0123 others(1): Show |
4 | HG02257.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1855+595A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916403 | |||||||
| chr5:154916666 | T | C | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1855+332A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916666 | |||||||
| chr5:154916688 | A | T | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1855+310T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916688 | |||||||
| chr5:154916777 | G | C | 1 | a0003c0003t0007g0286 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1855+221C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916777 | |||||||
| chr5:154916976 | G | C | 1 | a0002c0002t0001g0091 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1855+22C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916976 | |||||||
| chr5:154917228 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1674-49T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917228 | |||||||
| chr5:154917235 | A | C | 58 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(55): Show |
69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1674-56T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917235 | |||||||
| chr5:154917562 | G | A | 2 | a0006c0012t0002g0220 a0006c0012t0002g0221 |
2 | HG02280.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1673+369C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917562 | |||||||
| chr5:154917571 | T | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.1673+360A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917571 | |||||||
| chr5:154917697 | A | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | NA18978.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1673+234T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917697 | |||||||
| chr5:154917739 | G | A | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1673+192C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917739 | |||||||
| chr5:154917767 | C | T | 5 | a0004c0006t0001g0032 a0004c0006t0001g0273 a0004c0006t0001g0274 others(2): Show |
6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1673+164G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917767 | |||||||
| chr5:154917892 | C | T | 1 | a0003c0003t0001g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1673+39G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917892 | |||||||
| chr5:154918150 | G | A | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-146C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918150 | |||||||
| chr5:154918248 | G | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1600-244C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918248 | |||||||
| chr5:154918422 | C | G | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1600-418G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918422 | |||||||
| chr5:154918549 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.1600-545G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918549 | |||||||
| chr5:154918607 | G | T | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1600-603C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918607 | |||||||
| chr5:154918666 | G | C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1600-662C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918666 | |||||||
| chr5:154918794 | T | C | 16 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0255 others(13): Show |
18 | HG00438.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1600-790A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918794 | |||||||
| chr5:154918869 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1600-865G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918869 | |||||||
| chr5:154919194 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0172 |
2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1599+773C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154919194 | |||||||
| chr5:154919197 | G | T | 4 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0009c0031t0001g0069 others(1): Show |
4 | HG02015.hp1 HG02080.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1599+770C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154919197 | |||||||
| chr5:154919599 | T | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1599+368A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154919599 | |||||||
| chr5:154919619 | G | C | 2 | a0001c0001t0003g0244 a0001c0001t0003g0245 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1599+348C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154919619 | |||||||
| chr5:154919698 | C | T | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1599+269G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154919698 | |||||||
| chr5:154920179 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1463-76A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920179 | |||||||
| chr5:154920190 | A | G | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1463-87T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920190 | |||||||
| chr5:154920190 | A | T | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1463-87T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920190 | |||||||
| chr5:154920219 | A | C | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1463-116T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920219 | |||||||
| chr5:154920408 | T | A | 1 | a0001c0001t0001g0202 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1463-305A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920408 | |||||||
| chr5:154920474 | T | C | 2 | a0004c0006t0001g0275 a0004c0006t0001g0276 |
2 | HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1463-371A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920474 | |||||||
| chr5:154920644 | C | A | 1 | a0001c0001t0001g0166 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1463-541G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920644 | |||||||
| chr5:154921163 | C | G | 1 | a0001c0001t0001g0145 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1462+180G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154921163 | |||||||
| chr5:154921195 | T | G | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1462+148A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154921195 | |||||||
| chr5:154921285 | G | T | 2 | a0003c0009t0001g0040 a0003c0009t0001g0041 |
2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1462+58C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154921285 | |||||||
| chr5:154921565 | C | T | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1380-140G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154921565 | |||||||
| chr5:154921572 | T | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1380-147A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154921572 | |||||||
| chr5:154921911 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0097 others(7): Show |
14 | HG00140.hp2 HG00642.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1380-486C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154921911 | |||||||
| chr5:154921937 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1380-512T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154921937 | |||||||
| chr5:154921947 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1380-522T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154921947 | |||||||
| chr5:154922096 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1380-671T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922096 | |||||||
| chr5:154922180 | G | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.1380-755C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922180 | |||||||
| chr5:154922220 | T | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(59): Show |
75 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1380-795A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922220 | |||||||
| chr5:154922257 | T | C | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1380-832A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922257 | |||||||
| chr5:154922310 | G | T | 2 | a0003c0003t0001g0081 a0003c0003t0001g0082 |
2 | HG01952.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1380-885C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922310 | |||||||
| chr5:154922314 | C | A | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1380-889G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922314 | |||||||
| chr5:154922329 | G | A | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1380-904C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922329 | |||||||
| chr5:154922357 | T | C | 37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1380-932A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922357 | |||||||
| chr5:154922414 | G | A | 59 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(56): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.1380-989C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922414 | |||||||
| chr5:154922697 | G | GT | 48 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(45): Show |
53 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.1380-1273dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922697 | |||||||
| chr5:154922697 | G | GTT | 7 | a0002c0011t0001g0048 a0002c0018t0001g0046 a0003c0009t0001g0040 others(4): Show |
7 | HG01109.hp1 HG02109.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1380-1274_1380-127 others(6): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922697 | |||||||
| chr5:154922803 | TCTC | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1380-1381_1380-137 others(7): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922803 | |||||||
| chr5:154922841 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1380-1416G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922841 | |||||||
| chr5:154922938 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1380-1513G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922938 | |||||||
| chr5:154922942 | C | T | 3 | a0003c0005t0001g0077 a0003c0005t0001g0078 a0003c0005t0001g0079 |
3 | HG02055.hp1 HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1380-1517G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922942 | |||||||
| chr5:154922943 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | NA18973.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1380-1518C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922943 | |||||||
| chr5:154922985 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1379+1484G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922985 | |||||||
| chr5:154923217 | C | T | 6 | a0001c0004t0001g0119 a0001c0004t0001g0120 a0001c0004t0001g0121 others(3): Show |
6 | HG02257.hp2 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379+1252G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154923217 | |||||||
| chr5:154923355 | G | A | 1 | a0002c0002t0001g0067 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1379+1114C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154923355 | |||||||
| chr5:154923378 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1379+1091G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154923378 | |||||||
| chr5:154923609 | A | T | 37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1379+860T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154923609 | |||||||
| chr5:154923715 | C | T | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1379+754G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154923715 | |||||||
| chr5:154924049 | G | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1379+420C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154924049 | |||||||
| chr5:154924688 | A | C | 1 | a0001c0001t0001g0218 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1294-134T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924688 | |||||||
| chr5:154924732 | G | A | 2 | a0003c0003t0001g0088 a0003c0003t0001g0089 |
2 | HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1294-178C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924732 | |||||||
| chr5:154924771 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(143): Show |
174 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1294-217G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924771 | |||||||
| chr5:154924772 | G | A | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1294-218C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924772 | |||||||
| chr5:154924782 | G | C | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1294-228C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924782 | |||||||
| chr5:154924846 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.1294-292T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924846 | |||||||
| chr5:154924858 | G | A | 37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1294-304C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924858 | |||||||
| chr5:154924902 | A | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1294-348T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924902 | |||||||
| chr5:154924909 | A | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(220): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1294-355T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924909 | |||||||
| chr5:154924921 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1294-367C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924921 | |||||||
| chr5:154924938 | G | A | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1294-384C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924938 | |||||||
| chr5:154925214 | C | A | 1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1293+648G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154925214 | |||||||
| chr5:154925533 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1293+329C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154925533 | |||||||
| chr5:154925577 | T | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.1293+285A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154925577 | |||||||
| chr5:154925660 | G | A | 4 | a0003c0009t0001g0040 a0003c0009t0001g0041 a0003c0009t0001g0042 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1293+202C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154925660 | |||||||
| chr5:154925746 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1293+116A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154925746 | |||||||
| chr5:154926089 | G | A | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1081-15C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926089 | |||||||
| chr5:154926126 | G | GA | 5 | a0001c0001t0001g0181 a0003c0009t0001g0040 a0003c0009t0001g0041 others(2): Show |
5 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1081-53dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926126 | |||||||
| chr5:154926224 | A | G | 1 | a0002c0002t0001g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1081-150T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926224 | |||||||
| chr5:154926352 | G | T | 43 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(40): Show |
48 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1081-278C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926352 | |||||||
| chr5:154926387 | C | T | 1 | a0002c0018t0001g0046 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1081-313G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926387 | |||||||
| chr5:154926672 | G | A | 1 | a0001c0025t0001g0178 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1081-598C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926672 | |||||||
| chr5:154926766 | C | T | 43 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(40): Show |
48 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1080+619G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926766 | |||||||
| chr5:154926784 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1080+601C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926784 | |||||||
| chr5:154926833 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1080+552G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926833 | |||||||
| chr5:154927020 | C | T | 5 | a0002c0018t0001g0046 a0003c0009t0001g0040 a0003c0009t0001g0041 others(2): Show |
5 | HG01109.hp1 HG02109.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1080+365G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154927020 | |||||||
| chr5:154927052 | G | GA | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(257): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1080+332dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154927052 | |||||||
| chr5:154927052 | G | GAA | 7 | a0001c0001t0001g0097 a0001c0001t0001g0179 a0001c0001t0001g0203 others(4): Show |
7 | HG00621.hp1 HG00741.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1080+331_1080+332d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154927052 | |||||||
| chr5:154927237 | T | C | 2 | a0008c0010t0001g0033 a0008c0010t0001g0034 |
2 | NA18954.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1080+148A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154927237 | |||||||
| chr5:154927819 | G | A | 2 | a0001c0001t0002g0247 a0001c0001t0002g0248 |
2 | HG01099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.915-269C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154927819 | |||||||
| chr5:154927846 | TTGGGCAT others(2): Show |
T | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG01993.hp1 NA18978.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.915-305_915-297del others(9): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154927846 | |||||||
| chr5:154927925 | A | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(220): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.915-375T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154927925 | |||||||
| chr5:154927963 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.915-413G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154927963 | |||||||
| chr5:154928071 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | NA18954.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.914+456C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154928071 | |||||||
| chr5:154928223 | T | C | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.914+304A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154928223 | |||||||
| chr5:154928234 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0022 others(40): Show |
54 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.914+293C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154928234 | |||||||
| chr5:154928303 | T | C | 41 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(38): Show |
47 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.914+224A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154928303 | |||||||
| chr5:154928316 | A | C | 1 | a0001c0001t0001g0255 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.914+211T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154928316 | |||||||
| chr5:154928722 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(203): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.782-63G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154928722 | |||||||
| chr5:154928746 | C | T | 1 | a0002c0002t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.782-87G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154928746 | |||||||
| chr5:154928747 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(202): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.782-88C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154928747 | |||||||
| chr5:154928787 | C | A | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.782-128G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154928787 | |||||||
| chr5:154929141 | A | G | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG01070.hp1 HG01934.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.782-482T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929141 | |||||||
| chr5:154929415 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(221): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.782-756C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929415 | |||||||
| chr5:154929442 | C | T | 4 | a0003c0007t0001g0044 a0003c0007t0001g0045 a0003c0007t0001g0072 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.782-783G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929442 | |||||||
| chr5:154929556 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.782-897G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929556 | |||||||
| chr5:154929601 | C | G | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.782-942G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929601 | |||||||
| chr5:154929785 | A | C | 2 | a0006c0012t0002g0220 a0006c0012t0002g0221 |
2 | HG02280.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.782-1126T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929785 | |||||||
| chr5:154929958 | G | A | 37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.782-1299C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929958 | |||||||
| chr5:154930006 | T | C | 1 | a0002c0002t0001g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.782-1347A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930006 | |||||||
| chr5:154930025 | T | C | 1 | a0001c0014t0001g0209 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.782-1366A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930025 | |||||||
| chr5:154930131 | T | TCTGCCAT others(11): Show |
1 | a0003c0015t0008g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781+1309_781+1326d others(20): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930131 | |||||||
| chr5:154930188 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | NA18986.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.781+1270C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930188 | |||||||
| chr5:154930196 | C | A | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.781+1262G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930196 | |||||||
| chr5:154930283 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.781+1175C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930283 | |||||||
| chr5:154930364 | G | A | 1 | a0001c0030t0001g0213 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.781+1094C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930364 | |||||||
| chr5:154930788 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0006g0214 |
2 | HG04199.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.781+670C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930788 | |||||||
| chr5:154931446 | G | A | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.781+12C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154931446 | |||||||
| chr5:154931629 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.662-52A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154931629 | |||||||
| chr5:154931675 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(220): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.662-98A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154931675 | |||||||
| chr5:154931745 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.662-168A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154931745 | |||||||
| chr5:154931876 | G | A | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+223C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154931876 | |||||||
| chr5:154931906 | G | A | 1 | a0011c0019t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.661+193C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154931906 | |||||||
| chr5:154931948 | G | C | 1 | a0002c0002t0001g0071 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.661+151C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154931948 | |||||||
| chr5:154932016 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.661+83A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154932016 | |||||||
| chr5:154932338 | C | T | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.510-88G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932338 | |||||||
| chr5:154932417 | T | A | 1 | a0001c0001t0002g0249 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.510-167A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932417 | |||||||
| chr5:154932443 | T | G | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.510-193A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932443 | |||||||
| chr5:154932751 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.510-501T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932751 | |||||||
| chr5:154932816 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.510-566A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932816 | |||||||
| chr5:154932829 | T | C | 37 | a0002c0002t0001g0007 a0002c0002t0001g0011 a0002c0002t0001g0012 others(34): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.510-579A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932829 | |||||||
| chr5:154932871 | T | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.510-621A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932871 | |||||||
| chr5:154932902 | T | C | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.510-652A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932902 | |||||||
| chr5:154932966 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.510-716G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932966 | |||||||
| chr5:154932986 | C | T | 3 | a0002c0002t0001g0036 a0002c0002t0001g0037 a0002c0002t0001g0038 |
3 | NA18951.hp2 NA18998.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.510-736G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932986 | |||||||
| chr5:154932991 | T | C | 8 | a0001c0001t0001g0031 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
9 | HG00642.hp1 HG01070.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.510-741A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932991 | |||||||
| chr5:154933163 | C | T | 5 | a0004c0006t0001g0032 a0004c0006t0001g0273 a0004c0006t0001g0274 others(2): Show |
6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-913G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933163 | |||||||
| chr5:154933242 | C | T | 4 | a0003c0009t0001g0040 a0003c0009t0001g0041 a0003c0009t0001g0042 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-992G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933242 | |||||||
| chr5:154933273 | T | A | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.510-1023A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933273 | |||||||
| chr5:154933349 | G | T | 10 | a0001c0001t0001g0015 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
11 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-1099C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933349 | |||||||
| chr5:154933404 | A | G | 5 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | NA19006.hp1 NA19011.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-1154T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933404 | |||||||
| chr5:154933442 | G | A | 1 | a0003c0007t0001g0073 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.510-1192C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933442 | |||||||
| chr5:154933684 | A | AT | 6 | a0001c0001t0001g0097 a0001c0001t0001g0102 a0001c0001t0001g0104 others(3): Show |
6 | HG00323.hp2 HG00735.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.510-1435dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933684 | |||||||
| chr5:154933688 | T | A | 84 | a0001c0001t0001g0222 a0001c0001t0002g0003 a0001c0001t0002g0028 others(81): Show |
96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.510-1438A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933688 | |||||||
| chr5:154933697 | A | T | 2 | a0001c0001t0001g0268 a0003c0003t0001g0035 |
2 | HG00621.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.510-1447T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933697 | |||||||
| chr5:154933722 | C | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18950.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.510-1472G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933722 | |||||||
| chr5:154933769 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(265): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.510-1519T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933769 | |||||||
| chr5:154933839 | CCT | C | 43 | a0001c0004t0005g0039 a0002c0002t0001g0007 a0002c0002t0001g0011 others(40): Show |
48 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.510-1591_510-1590d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933839 | |||||||
| chr5:154933864 | G | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.510-1614C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933864 | |||||||
| chr5:154934106 | C | A | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.509+1735G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934106 | |||||||
| chr5:154934164 | C | A | 2 | a0003c0007t0001g0072 a0003c0007t0001g0073 |
2 | HG00558.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.509+1677G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934164 | |||||||
| chr5:154934165 | G | A | 1 | a0003c0023t0001g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.509+1676C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934165 | |||||||
| chr5:154934293 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(266): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.509+1548G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934293 | |||||||
| chr5:154934513 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.509+1328A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934513 | |||||||
| chr5:154934529 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
9 | HG00140.hp2 HG00642.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+1312G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934529 | |||||||
| chr5:154934604 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.509+1237C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934604 | |||||||
| chr5:154934637 | G | A | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+1204C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934637 | |||||||
| chr5:154934659 | T | C | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.509+1182A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934659 | |||||||
| chr5:154934706 | C | T | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.509+1135G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934706 | |||||||
| chr5:154934782 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.509+1059A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934782 | |||||||
| chr5:154934796 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.509+1045T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934796 | |||||||
| chr5:154935032 | C | T | 4 | a0003c0009t0001g0040 a0003c0009t0001g0041 a0003c0009t0001g0042 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+809G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935032 | |||||||
| chr5:154935072 | T | A | 4 | a0002c0002t0001g0013 a0002c0002t0001g0074 a0002c0002t0001g0075 others(1): Show |
5 | HG01346.hp2 HG01993.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+769A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935072 | |||||||
| chr5:154935306 | T | C | 4 | a0003c0009t0001g0040 a0003c0009t0001g0041 a0003c0009t0001g0042 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+535A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935306 | |||||||
| chr5:154935508 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18950.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.509+333T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935508 | |||||||
| chr5:154935533 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.509+308C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935533 | |||||||
| chr5:154935620 | A | G | 4 | a0003c0009t0001g0040 a0003c0009t0001g0041 a0003c0009t0001g0042 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+221T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935620 | |||||||
| chr5:154935791 | C | G | 2 | a0001c0004t0005g0039 a0003c0003t0001g0035 |
2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.509+50G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935791 | |||||||
| chr5:154935794 | G | A | 16 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0255 others(13): Show |
18 | HG00438.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.509+47C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935794 | |||||||
| chr5:154936099 | A | C | 1 | a0001c0001t0001g0014 | 2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.328-77T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936099 | |||||||
| chr5:154936310 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.328-288C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936310 | |||||||
| chr5:154936357 | CAGTGAGC others(78): Show |
C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.328-420_328-336del others(85): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936357 | |||||||
| chr5:154936416 | C | CAAAAAAA | 17 | a0003c0003t0001g0004 a0003c0003t0001g0010 a0003c0003t0001g0035 others(14): Show |
20 | HG01952.hp1 HG01978.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.328-401_328-395dup others(7): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936416 | |||||||
| chr5:154936706 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG02074.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.327+319C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936706 | |||||||
| chr5:154936819 | A | C | 3 | a0002c0002t0001g0036 a0002c0002t0001g0037 a0002c0002t0001g0038 |
3 | NA18951.hp2 NA18998.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.327+206T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936819 | |||||||
| chr5:154936951 | A | G | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.327+74T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936951 | |||||||
| chr5:154937003 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.327+22T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154937003 | |||||||
| chr5:154937365 | G | A | 1 | a0001c0029t0002g0277 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.167-180C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937365 | |||||||
| chr5:154937393 | T | C | 3 | a0002c0002t0001g0007 a0002c0002t0001g0090 a0002c0002t0001g0091 |
5 | HG02257.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.167-208A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937393 | |||||||
| chr5:154937482 | T | C | 1 | a0002c0021t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.167-297A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937482 | |||||||
| chr5:154937499 | T | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(218): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.167-314A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937499 | |||||||
| chr5:154937520 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.167-335A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937520 | |||||||
| chr5:154937594 | T | C | 1 | a0012c0017t0004g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.166+374A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937594 | |||||||
| chr5:154937797 | T | C | 1 | a0001c0001t0001g0280 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.166+171A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937797 | |||||||
| chr5:154937884 | G | A | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG00323.hp1 HG01106.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.166+84C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937884 |