Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84340 |
| ensemblid | ENSG00000164347.18 |
| hgncid | 29682 |
| symbol | GFM2 |
| name | GTP dependent ribosome recycling factor mitochondrial 2 |
| refseq_nuc | NM_032380.5 |
| refseq_prot | NP_115756.2 |
| ensembl_nuc | ENST00000296805.8 |
| ensembl_prot | ENSP00000296805.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 74721206 |
| end | 74767117 |
| strand | - |
| ver | v1.2 |
| region | chr5:74721206-74767117 |
| region5000 | chr5:74716206-74772117 |
| regionname0 | GFM2_chr5_74721206_74767117 |
| regionname5000 | GFM2_chr5_74716206_74772117 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 779 | 201 | 25 | 42 | 98 | 9 | 26 | 69 | GFM2_chr5_74716206_74772117 | GFM2 | MLTNL others(774): Show |
chr5 | 74716206 | 74772117 |
| a0002 | 0/0 | 777 | 103 | 45 | 18 | 35 | 1 | 4 | 24 | GFM2_chr5_74716206_74772117 | GFM2 | MLTNL others(772): Show |
chr5 | 74716206 | 74772117 |
| a0003 | 0/1 | 777 | 33 | 10 | 11 | 2 | 4 | 5 | 2 | GFM2_chr5_74716206_74772117 | GFM2 | MLTNL others(772): Show |
chr5 | 74716206 | 74772117 |
| a0004 | 0/0 | 777 | 13 | 10 | 3 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | MLTNL others(772): Show |
chr5 | 74716206 | 74772117 |
| a0005 | 0/0 | 779 | 13 | 0 | 0 | 13 | 0 | 0 | 13 | GFM2_chr5_74716206_74772117 | GFM2 | MLTNL others(774): Show |
chr5 | 74716206 | 74772117 |
| a0006 | 0/0 | 779 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | GFM2_chr5_74716206_74772117 | GFM2 | MLTNL others(774): Show |
chr5 | 74716206 | 74772117 |
| a0007 | 0/0 | 779 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | MLTNL others(774): Show |
chr5 | 74716206 | 74772117 |
| a0008 | 0/0 | 779 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | MLTNL others(774): Show |
chr5 | 74716206 | 74772117 |
| a0009 | 0/0 | 777 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | MLTNL others(772): Show |
chr5 | 74716206 | 74772117 |
| a0010 | 0/0 | 779 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | MLTNL others(774): Show |
chr5 | 74716206 | 74772117 |
| a0011 | 0/0 | 779 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | MLTNL others(774): Show |
chr5 | 74716206 | 74772117 |
| a0012 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | MLTNL others(772): Show |
chr5 | 74716206 | 74772117 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2337 | 198 | 25 | 42 | 95 | 9 | 26 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2332): Show |
chr5 | 74716206 | 74772117 | ||
| a0001c0011 | 0/0 | 2337 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2332): Show |
chr5 | 74716206 | 74772117 | ||
| a0001c0020 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2332): Show |
chr5 | 74716206 | 74772117 | ||
| a0002c0002 | 0/0 | 2331 | 73 | 19 | 16 | 33 | 1 | 4 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 | ||
| a0002c0005 | 0/0 | 2331 | 13 | 13 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 | ||
| a0002c0006 | 0/0 | 2331 | 11 | 11 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 | ||
| a0002c0008 | 0/0 | 2331 | 4 | 0 | 2 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 | ||
| a0002c0017 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 | ||
| a0002c0019 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 | ||
| a0003c0003 | 0/1 | 2331 | 31 | 9 | 10 | 2 | 4 | 5 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 | ||
| a0003c0013 | 0/0 | 2331 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 | ||
| a0004c0007 | 0/0 | 2331 | 7 | 5 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 | ||
| a0004c0009 | 0/0 | 2331 | 4 | 4 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 | ||
| a0004c0012 | 0/0 | 2331 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 | ||
| a0005c0004 | 0/0 | 2337 | 13 | 0 | 0 | 13 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2332): Show |
chr5 | 74716206 | 74772117 | ||
| a0006c0010 | 0/0 | 2337 | 3 | 0 | 0 | 3 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2332): Show |
chr5 | 74716206 | 74772117 | ||
| a0007c0021 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2332): Show |
chr5 | 74716206 | 74772117 | ||
| a0008c0022 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2332): Show |
chr5 | 74716206 | 74772117 | ||
| a0009c0016 | 0/0 | 2331 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 | ||
| a0010c0014 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2332): Show |
chr5 | 74716206 | 74772117 | ||
| a0011c0018 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2332): Show |
chr5 | 74716206 | 74772117 | ||
| a0012c0015 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | ATGTT others(2326): Show |
chr5 | 74716206 | 74772117 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2993 | 179 | 24 | 36 | 84 | 8 | 26 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2988): Show |
chr5 | 74716206 | 74772117 |
| a0001c0001t0003 | 0/0 | 2991 | 19 | 1 | 6 | 11 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2986): Show |
chr5 | 74716206 | 74772117 |
| a0001c0011t0002 | 0/0 | 2993 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2988): Show |
chr5 | 74716206 | 74772117 |
| a0001c0020t0001 | 0/0 | 2993 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2988): Show |
chr5 | 74716206 | 74772117 |
| a0002c0002t0001 | 0/0 | 2987 | 20 | 17 | 3 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0002c0002t0002 | 0/0 | 2987 | 52 | 2 | 13 | 32 | 1 | 4 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0002c0002t0004 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0002c0005t0001 | 0/0 | 2987 | 13 | 13 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0002c0006t0001 | 0/0 | 2987 | 11 | 11 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0002c0008t0001 | 0/0 | 2987 | 4 | 0 | 2 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0002c0017t0001 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0002c0019t0001 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0003c0003t0001 | 0/1 | 2987 | 31 | 9 | 10 | 2 | 4 | 5 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0003c0013t0001 | 0/0 | 2987 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0004c0007t0001 | 0/0 | 2987 | 7 | 5 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0004c0009t0001 | 0/0 | 2987 | 4 | 4 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0004c0012t0001 | 0/0 | 2987 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0005c0004t0001 | 0/0 | 2993 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2988): Show |
chr5 | 74716206 | 74772117 |
| a0005c0004t0003 | 0/0 | 2991 | 12 | 0 | 0 | 12 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2986): Show |
chr5 | 74716206 | 74772117 |
| a0006c0010t0001 | 0/0 | 2993 | 3 | 0 | 0 | 3 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2988): Show |
chr5 | 74716206 | 74772117 |
| a0007c0021t0001 | 0/0 | 2993 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2988): Show |
chr5 | 74716206 | 74772117 |
| a0008c0022t0003 | 0/0 | 2991 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2986): Show |
chr5 | 74716206 | 74772117 |
| a0009c0016t0002 | 0/0 | 2987 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| a0010c0014t0003 | 0/0 | 2991 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2986): Show |
chr5 | 74716206 | 74772117 |
| a0011c0018t0001 | 0/0 | 2993 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2988): Show |
chr5 | 74716206 | 74772117 |
| a0012c0015t0002 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | GGTGT others(2982): Show |
chr5 | 74716206 | 74772117 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 6 | 0 | 2 | 3 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0011 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0007 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0011t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0011t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0001c0020t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0002 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0009 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0005t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0005t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0005t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0005t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0005t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0005t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0005t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0005t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0005t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0005t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0006t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0006t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0006t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0006t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0006t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0006t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0006t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0006t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0006t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0006t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0008t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0008t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0008t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0008t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0017t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0002c0019t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0008 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0280 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0013t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0003c0013t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0004c0007t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0004c0007t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0004c0007t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0004c0007t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0004c0007t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0004c0007t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0004c0009t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0004c0009t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0004c0009t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0004c0012t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0004c0012t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0005c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0005c0004t0003g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0005c0004t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0005c0004t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0005c0004t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0005c0004t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0005c0004t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0005c0004t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0005c0004t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0005c0004t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0006c0010t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0006c0010t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0006c0010t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0007c0021t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0008c0022t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0009c0016t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0010c0014t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0011c0018t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| a0012c0015t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0083 | EUR | GBR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0290 | EUR | GBR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0288 | EUR | FIN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00438 | hp2 | a0002 | c0008 | t0001 | g0135 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00642 | hp2 | a0004 | c0012 | t0001 | g0293 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00733 | hp2 | a0004 | c0007 | t0001 | g0271 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00735 | hp2 | a0002 | c0008 | t0001 | g0170 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0273 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01069 | hp1 | a0003 | c0003 | t0001 | g0287 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0014 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0084 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0283 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01167 | hp2 | a0003 | c0003 | t0001 | g0013 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0013 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0062 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01243 | hp1 | a0004 | c0007 | t0001 | g0039 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01243 | hp2 | a0003 | c0013 | t0001 | g0292 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0286 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0274 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0014 | EUR | IBS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0014 | EUR | IBS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0237 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01891 | hp1 | a0002 | c0005 | t0001 | g0230 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0063 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0048 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01952 | hp1 | a0007 | c0021 | t0001 | g0206 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01978 | hp1 | a0008 | c0022 | t0003 | g0267 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02083 | hp2 | a0001 | c0020 | t0001 | g0099 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02145 | hp2 | a0002 | c0005 | t0001 | g0301 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02148 | hp1 | a0003 | c0003 | t0001 | g0279 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | CDX | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0254 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0241 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02293 | hp1 | a0002 | c0008 | t0001 | g0171 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0066 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02451 | hp1 | a0004 | c0009 | t0001 | g0155 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02451 | hp2 | a0002 | c0005 | t0001 | g0036 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02572 | hp2 | a0003 | c0003 | t0001 | g0276 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02615 | hp2 | a0002 | c0006 | t0001 | g0144 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0040 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02630 | hp2 | a0002 | c0005 | t0001 | g0243 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02717 | hp1 | a0004 | c0009 | t0001 | g0021 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02717 | hp2 | a0004 | c0007 | t0001 | g0268 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02723 | hp1 | a0002 | c0005 | t0001 | g0042 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02723 | hp2 | a0002 | c0006 | t0001 | g0139 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0041 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0239 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0296 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0071 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02886 | hp1 | a0002 | c0005 | t0001 | g0302 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02886 | hp2 | a0002 | c0019 | t0001 | g0145 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0148 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0285 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0013 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0291 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02965 | hp2 | a0004 | c0012 | t0001 | g0281 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02976 | hp2 | a0002 | c0006 | t0001 | g0137 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03098 | hp1 | a0004 | c0009 | t0001 | g0154 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0232 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03130 | hp1 | a0002 | c0006 | t0001 | g0141 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03139 | hp1 | a0002 | c0006 | t0001 | g0140 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03139 | hp2 | a0002 | c0005 | t0001 | g0036 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03195 | hp2 | a0002 | c0005 | t0001 | g0304 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0242 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03225 | hp2 | a0003 | c0013 | t0001 | g0284 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0282 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03453 | hp1 | a0002 | c0006 | t0001 | g0142 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03453 | hp2 | a0002 | c0005 | t0001 | g0231 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03486 | hp1 | a0002 | c0006 | t0001 | g0138 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03486 | hp2 | a0004 | c0007 | t0001 | g0270 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03491 | hp1 | a0009 | c0016 | t0002 | g0055 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03516 | hp2 | a0002 | c0005 | t0001 | g0244 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0149 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03579 | hp1 | a0002 | c0006 | t0001 | g0143 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03579 | hp2 | a0002 | c0005 | t0001 | g0300 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0041 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03710 | hp1 | a0003 | c0003 | t0001 | g0278 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03831 | hp1 | a0003 | c0003 | t0001 | g0277 | SAS | BEB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0009 | SAS | BEB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0056 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0053 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18522 | hp1 | a0002 | c0017 | t0001 | g0146 | AFR | YRI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | YRI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0289 | AFR | YRI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18943 | hp2 | a0005 | c0004 | t0003 | g0247 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18944 | hp2 | a0005 | c0004 | t0003 | g0248 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18948 | hp1 | a0002 | c0002 | t0004 | g0067 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18962 | hp1 | a0005 | c0004 | t0003 | g0006 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18963 | hp2 | a0010 | c0014 | t0003 | g0257 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18969 | hp2 | a0006 | c0010 | t0001 | g0221 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18970 | hp1 | a0001 | c0011 | t0002 | g0073 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18977 | hp1 | a0005 | c0004 | t0001 | g0260 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18982 | hp1 | a0011 | c0018 | t0001 | g0172 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18986 | hp1 | a0005 | c0004 | t0003 | g0256 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18994 | hp2 | a0005 | c0004 | t0003 | g0249 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18995 | hp2 | a0001 | c0011 | t0002 | g0044 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18998 | hp2 | a0006 | c0010 | t0001 | g0233 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19001 | hp1 | a0002 | c0008 | t0001 | g0173 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19003 | hp1 | a0003 | c0003 | t0001 | g0040 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19006 | hp2 | a0012 | c0015 | t0002 | g0057 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19007 | hp2 | a0005 | c0004 | t0003 | g0006 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19009 | hp2 | a0005 | c0004 | t0003 | g0006 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19030 | hp1 | a0004 | c0007 | t0001 | g0269 | AFR | LWK | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19030 | hp2 | a0002 | c0006 | t0001 | g0136 | AFR | LWK | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0275 | AFR | LWK | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | LWK | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19056 | hp2 | a0005 | c0004 | t0003 | g0259 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19063 | hp2 | a0005 | c0004 | t0003 | g0258 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19075 | hp1 | a0005 | c0004 | t0003 | g0261 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19080 | hp1 | a0005 | c0004 | t0003 | g0006 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19085 | hp1 | a0006 | c0010 | t0001 | g0189 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19090 | hp2 | a0005 | c0004 | t0003 | g0262 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19240 | hp1 | a0002 | c0005 | t0001 | g0042 | AFR | YRI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA20129 | hp1 | a0004 | c0009 | t0001 | g0021 | AFR | ASW | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ASW | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0007 | EUR | TSI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | GIH | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | GIH | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02109 | hp2 | a0004 | c0007 | t0001 | g0272 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0134 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02559 | hp1 | a0002 | c0006 | t0001 | g0128 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG02559 | hp2 | a0002 | c0005 | t0001 | g0303 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| HG03471 | hp2 | a0004 | c0007 | t0001 | g0039 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA20300 | hp1 | a0002 | c0006 | t0001 | g0133 | AFR | USA | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0064 | AFR | USA | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | LWK | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0280 | REF | REF | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74721674 | C | T | 3 | a0002 a0003 a0004 |
35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
missense_variant | MODERATE | c.2321G>A | p.Arg774Gln | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 21/21 | 2525/2993 | 2321/2340 | 774/779 | chr5 | 74721674 | |||
| chr5:74721765 | G | C | 2 | a0002 a0011 |
5 | HG00438.hp2 HG00735.hp2 HG02293.hp1 others(2): Show |
missense_variant | MODERATE | c.2230C>G | p.Arg744Gly | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 21/21 | 2434/2993 | 2230/2340 | 744/779 | chr5 | 74721765 | |||
| chr5:74721782 | C | T | 1 | a0010 | 1 | NA18963.hp2 | missense_variant&splice_region_variant | MODERATE | c.2213G>A | p.Gly738Asp | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 21/21 | 2417/2993 | 2213/2340 | 738/779 | chr5 | 74721782 | |||
| chr5:74725968 | T | C | 1 | a0002 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.1885A>G | p.Asn629Asp | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 18/21 | 2089/2993 | 1885/2340 | 629/779 | chr5 | 74725968 | |||
| chr5:74725973 | A | G | 1 | a0003 | 2 | HG01243.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.1880T>C | p.Ile627Thr | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 18/21 | 2084/2993 | 1880/2340 | 627/779 | chr5 | 74725973 | |||
| chr5:74726021 | TACTCAA | T | 5 | a0002 a0003 a0004 others(2): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
disruptive_inframe_deletion | MODERATE | c.1826_1831delTTGAGT | p.Phe609_Glu610del | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 18/21 | 2035/2993 | 1826/2340 | 609/779 | chr5 | 74726021 | |||
| chr5:74726093 | T | G | 1 | a0007 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.1760A>C | p.His587Pro | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 18/21 | 1964/2993 | 1760/2340 | 587/779 | chr5 | 74726093 | |||
| chr5:74738526 | A | G | 1 | a0010 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.1196T>C | p.Ile399Thr | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 13/21 | 1400/2993 | 1196/2340 | 399/779 | chr5 | 74738526 | |||
| chr5:74738620 | A | G | 1 | a0009 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.1102T>C | p.Cys368Arg | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 13/21 | 1306/2993 | 1102/2340 | 368/779 | chr5 | 74738620 | |||
| chr5:74738628 | T | C | 1 | a0006 | 3 | NA18969.hp2 NA18998.hp2 NA19085.hp1 |
missense_variant | MODERATE | c.1094A>G | p.Asp365Gly | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 13/21 | 1298/2993 | 1094/2340 | 365/779 | chr5 | 74738628 | |||
| chr5:74741561 | T | A | 1 | a0003 | 32 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(29): Show |
missense_variant | MODERATE | c.898A>T | p.Ser300Cys | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/21 | 1102/2993 | 898/2340 | 300/779 | chr5 | 74741561 | |||
| chr5:74745683 | C | T | 1 | a0012 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.844G>A | p.Glu282Lys | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/21 | 1048/2993 | 844/2340 | 282/779 | chr5 | 74745683 | |||
| chr5:74759384 | T | C | 2 | a0003 a0004 |
45 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(42): Show |
missense_variant | MODERATE | c.191A>G | p.Asn64Ser | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/21 | 395/2993 | 191/2340 | 64/779 | chr5 | 74759384 | |||
| chr5:74759397 | G | T | 2 | a0005 a0010 |
14 | NA18943.hp2 NA18944.hp2 NA18962.hp1 others(11): Show |
missense_variant | MODERATE | c.178C>A | p.His60Asn | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/21 | 382/2993 | 178/2340 | 60/779 | chr5 | 74759397 | |||
| chr5:74763700 | T | C | 1 | a0008 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.43A>G | p.Ile15Val | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/21 | 247/2993 | 43/2340 | 15/779 | chr5 | 74763700 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74726038 | A | G | 1 | a0001c0020 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1815T>C | p.Pro605Pro | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 18/21 | 2019/2993 | 1815/2340 | 605/779 | chr5 | 74726038 | |||
| chr5:74741544 | C | T | 2 | a0002c0006 a0002c0019 |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
synonymous_variant | LOW | c.915G>A | p.Leu305Leu | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/21 | 1119/2993 | 915/2340 | 305/779 | chr5 | 74741544 | |||
| chr5:74750639 | C | T | 8 | a0001c0011 a0002c0002 a0002c0008 others(5): Show |
87 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
synonymous_variant | LOW | c.459G>A | p.Glu153Glu | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/21 | 663/2993 | 459/2340 | 153/779 | chr5 | 74750639 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74721255 | CTG | C | 4 | a0001c0001t0003 a0005c0004t0003 a0008c0022t0003 others(1): Show |
33 | HG00673.hp1 HG00741.hp1 HG01123.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*398_*399delCA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 21/21 | 398 | chr5 | 74721255 | ||||||
| chr5:74721282 | G | A | 1 | a0002c0002t0004 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 21/21 | 373 | chr5 | 74721282 | ||||||
| chr5:74767056 | C | T | 5 | a0001c0011t0002 a0002c0002t0002 a0002c0002t0004 others(2): Show |
57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-143G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/21 | 3314 | chr5 | 74767056 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74721963 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2212-180C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 20/20 | chr5 | 74721963 | |||||||
| chr5:74721983 | T | C | 6 | a0004c0007t0001g0039 a0004c0007t0001g0268 a0004c0007t0001g0269 others(3): Show |
7 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2212-200A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 20/20 | chr5 | 74721983 | |||||||
| chr5:74722252 | A | AAACTT | 3 | a0001c0001t0001g0028 a0001c0001t0001g0180 a0001c0001t0001g0224 |
4 | HG00323.hp1 HG02683.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.2211+122_2211+126d others(7): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 20/20 | chr5 | 74722252 | |||||||
| chr5:74722344 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2211+35C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 20/20 | chr5 | 74722344 | |||||||
| chr5:74722853 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2029-292T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74722853 | |||||||
| chr5:74722949 | A | C | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2029-388T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74722949 | |||||||
| chr5:74723035 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2029-474A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74723035 | |||||||
| chr5:74723137 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2029-576T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74723137 | |||||||
| chr5:74723160 | C | T | 1 | a0006c0010t0001g0233 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2029-599G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74723160 | |||||||
| chr5:74723377 | A | G | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2029-816T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74723377 | |||||||
| chr5:74723781 | C | T | 4 | a0002c0008t0001g0135 a0002c0008t0001g0170 a0002c0008t0001g0171 others(1): Show |
4 | HG00438.hp2 HG00735.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2029-1220G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74723781 | |||||||
| chr5:74724204 | C | T | 73 | a0002c0002t0001g0020 a0002c0002t0001g0134 a0002c0002t0001g0147 others(70): Show |
84 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.2028+1436G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724204 | |||||||
| chr5:74724394 | T | C | 2 | a0001c0001t0003g0037 a0001c0001t0003g0252 |
3 | NA18965.hp2 NA18987.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2028+1246A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724394 | |||||||
| chr5:74724410 | G | A | 8 | a0003c0003t0001g0014 a0003c0003t0001g0273 a0003c0003t0001g0274 others(5): Show |
10 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.2028+1230C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724410 | |||||||
| chr5:74724473 | T | TA | 20 | a0001c0001t0001g0180 a0001c0001t0001g0203 a0001c0001t0001g0224 others(17): Show |
23 | HG01175.hp1 HG01175.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.2028+1166dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724473 | |||||||
| chr5:74724473 | TA | T | 54 | a0001c0001t0001g0211 a0001c0001t0003g0252 a0002c0002t0002g0015 others(51): Show |
66 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.2028+1166delT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724473 | |||||||
| chr5:74724678 | T | G | 1 | a0004c0007t0001g0271 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2028+962A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724678 | |||||||
| chr5:74724720 | C | T | 1 | a0002c0006t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2028+920G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724720 | |||||||
| chr5:74724915 | G | A | 1 | a0002c0002t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2028+725C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724915 | |||||||
| chr5:74724987 | C | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0096 a0001c0001t0001g0100 others(1): Show |
8 | HG01928.hp1 HG01943.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2028+653G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724987 | |||||||
| chr5:74725310 | G | A | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2028+330C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74725310 | |||||||
| chr5:74725376 | T | C | 4 | a0002c0002t0002g0053 a0002c0002t0002g0082 a0002c0002t0002g0083 others(1): Show |
4 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2028+264A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74725376 | |||||||
| chr5:74725499 | T | C | 1 | a0002c0002t0002g0071 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2028+141A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74725499 | |||||||
| chr5:74725930 | G | A | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1912+11C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 18/20 | chr5 | 74725930 | |||||||
| chr5:74726280 | CAGAG | C | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1727-158_1727-155d others(6): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74726280 | |||||||
| chr5:74726313 | T | C | 2 | a0003c0003t0001g0277 a0003c0003t0001g0278 |
2 | HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1727-187A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74726313 | |||||||
| chr5:74726525 | G | T | 48 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0002g0002 others(45): Show |
57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1727-399C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74726525 | |||||||
| chr5:74726644 | T | C | 1 | a0002c0002t0002g0078 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1727-518A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74726644 | |||||||
| chr5:74726807 | G | C | 1 | a0002c0005t0001g0036 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1727-681C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74726807 | |||||||
| chr5:74726841 | C | T | 14 | a0002c0002t0001g0020 a0002c0002t0001g0134 a0002c0002t0001g0147 others(11): Show |
16 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1727-715G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74726841 | |||||||
| chr5:74727216 | C | T | 126 | a0002c0002t0001g0020 a0002c0002t0001g0134 a0002c0002t0001g0147 others(123): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1727-1090G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727216 | |||||||
| chr5:74727304 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1727-1178T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727304 | |||||||
| chr5:74727655 | A | C | 2 | a0001c0011t0002g0044 a0001c0011t0002g0073 |
2 | NA18970.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1727-1529T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727655 | |||||||
| chr5:74727815 | T | C | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1727-1689A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727815 | |||||||
| chr5:74727858 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0169 a0001c0001t0001g0199 others(1): Show |
5 | HG00408.hp1 HG02040.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1727-1732T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727858 | |||||||
| chr5:74727975 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0124 a0001c0001t0001g0127 |
3 | HG02165.hp2 NA19006.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1727-1849C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727975 | |||||||
| chr5:74727994 | T | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0116 a0001c0001t0001g0122 others(1): Show |
4 | NA18612.hp2 NA18947.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1727-1868A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727994 | |||||||
| chr5:74728057 | G | A | 1 | a0002c0002t0001g0020 | 2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1727-1931C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728057 | |||||||
| chr5:74728115 | C | T | 1 | a0005c0004t0003g0259 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1727-1989G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728115 | |||||||
| chr5:74728209 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1726+2051A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728209 | |||||||
| chr5:74728349 | G | GT | 48 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0002g0002 others(45): Show |
57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1726+1910dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728349 | |||||||
| chr5:74728395 | A | T | 1 | a0002c0006t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1726+1865T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728395 | |||||||
| chr5:74728591 | A | C | 1 | a0002c0002t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1726+1669T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728591 | |||||||
| chr5:74728748 | C | CT | 74 | a0001c0001t0001g0018 a0001c0001t0001g0088 a0001c0001t0001g0089 others(71): Show |
86 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.1726+1511dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | |||||||
| chr5:74728748 | C | CTT | 23 | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0001g0111 others(20): Show |
23 | HG00621.hp2 HG01109.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1726+1510_1726+151 others(6): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | |||||||
| chr5:74728748 | CT | C | 9 | a0001c0001t0001g0027 a0001c0001t0001g0124 a0001c0001t0001g0126 others(6): Show |
10 | HG01943.hp2 HG02523.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1726+1511delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | |||||||
| chr5:74728748 | CTT | C | 6 | a0002c0002t0001g0237 a0002c0002t0001g0238 a0002c0002t0001g0239 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1726+1510_1726+151 others(6): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | |||||||
| chr5:74728748 | CTTTTTT | C | 7 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(4): Show |
9 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1726+1506_1726+151 others(10): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | |||||||
| chr5:74728748 | CTTTTTTT others(2): Show |
C | 13 | a0001c0001t0001g0156 a0001c0001t0001g0176 a0001c0001t0001g0183 others(10): Show |
13 | HG00735.hp1 HG02148.hp2 HG03225.hp1 others(10): Show |
intron_variant | MODIFIER | c.1726+1503_1726+151 others(13): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | |||||||
| chr5:74728748 | CTTTTTTT others(9): Show |
C | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1726+1496_1726+151 others(20): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | |||||||
| chr5:74728759 | T | C | 14 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(11): Show |
17 | HG00621.hp1 HG02080.hp2 NA18943.hp2 others(14): Show |
intron_variant | MODIFIER | c.1726+1501A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728759 | |||||||
| chr5:74728770 | T | TTTTTTTG others(3): Show |
26 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(23): Show |
36 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.1726+1489_1726+149 others(14): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728770 | |||||||
| chr5:74728770 | T | TTTTTTTT others(4): Show |
4 | a0003c0003t0001g0279 a0003c0003t0001g0283 a0003c0003t0001g0289 others(1): Show |
4 | HG00642.hp2 HG01109.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726+1489_1726+149 others(15): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728770 | |||||||
| chr5:74728826 | A | G | 1 | a0002c0017t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1726+1434T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728826 | |||||||
| chr5:74728973 | C | G | 3 | a0002c0002t0001g0238 a0002c0002t0001g0239 a0002c0002t0001g0242 |
3 | HG02809.hp1 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1726+1287G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728973 | |||||||
| chr5:74729044 | A | G | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1726+1216T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729044 | |||||||
| chr5:74729048 | G | A | 70 | a0002c0002t0001g0020 a0002c0002t0001g0134 a0002c0002t0001g0147 others(67): Show |
81 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1726+1212C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729048 | |||||||
| chr5:74729110 | T | C | 1 | a0004c0007t0001g0268 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1726+1150A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729110 | |||||||
| chr5:74729129 | G | A | 3 | a0002c0002t0001g0174 a0002c0002t0001g0232 a0002c0002t0001g0236 |
3 | HG03041.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1726+1131C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729129 | |||||||
| chr5:74729168 | G | A | 1 | a0002c0002t0002g0048 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1726+1092C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729168 | |||||||
| chr5:74729236 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1726+1024A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729236 | |||||||
| chr5:74729325 | A | G | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1726+935T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729325 | |||||||
| chr5:74729441 | A | G | 128 | a0002c0002t0001g0020 a0002c0002t0001g0134 a0002c0002t0001g0147 others(125): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1726+819T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729441 | |||||||
| chr5:74729483 | A | G | 1 | a0002c0017t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1726+777T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729483 | |||||||
| chr5:74729678 | C | CT | 27 | a0002c0002t0001g0151 a0002c0005t0001g0036 a0002c0005t0001g0042 others(24): Show |
29 | HG00438.hp2 HG00735.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1726+581dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729678 | |||||||
| chr5:74729678 | C | CTT | 66 | a0002c0002t0001g0020 a0002c0002t0001g0134 a0002c0002t0001g0147 others(63): Show |
77 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.1726+580_1726+581d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729678 | |||||||
| chr5:74729678 | CT | C | 7 | a0001c0001t0001g0113 a0001c0001t0001g0198 a0001c0001t0001g0226 others(4): Show |
9 | HG01074.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1726+581delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729678 | |||||||
| chr5:74729819 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1726+441G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729819 | |||||||
| chr5:74729893 | T | C | 3 | a0002c0002t0001g0174 a0002c0002t0001g0232 a0002c0002t0001g0236 |
3 | HG03041.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1726+367A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729893 | |||||||
| chr5:74730551 | T | C | 6 | a0002c0002t0001g0237 a0002c0002t0001g0238 a0002c0002t0001g0239 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588-153A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74730551 | |||||||
| chr5:74730838 | A | T | 1 | a0001c0001t0001g0202 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1588-440T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74730838 | |||||||
| chr5:74730845 | C | T | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1588-447G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74730845 | |||||||
| chr5:74730850 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1588-452C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74730850 | |||||||
| chr5:74731059 | T | C | 54 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0230 others(51): Show |
66 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.1588-661A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731059 | |||||||
| chr5:74731194 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1588-796T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731194 | |||||||
| chr5:74731357 | G | T | 1 | a0002c0008t0001g0171 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1588-959C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731357 | |||||||
| chr5:74731423 | C | T | 1 | a0001c0001t0003g0264 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1588-1025G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731423 | |||||||
| chr5:74731611 | T | G | 11 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0137 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1588-1213A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731611 | |||||||
| chr5:74731620 | T | TA | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1588-1223dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731620 | |||||||
| chr5:74731872 | C | T | 1 | a0003c0003t0001g0289 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1587+1150G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731872 | |||||||
| chr5:74732128 | A | AT | 21 | a0001c0001t0001g0011 a0001c0001t0001g0090 a0001c0001t0001g0119 others(18): Show |
23 | HG01099.hp2 HG01168.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1587+893dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732128 | |||||||
| chr5:74732128 | AT | A | 26 | a0001c0001t0001g0211 a0001c0001t0003g0255 a0002c0002t0002g0080 others(23): Show |
35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1587+893delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732128 | |||||||
| chr5:74732315 | T | A | 1 | a0005c0004t0003g0262 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1587+707A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732315 | |||||||
| chr5:74732417 | T | G | 1 | a0001c0001t0003g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1587+605A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732417 | |||||||
| chr5:74732453 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1587+569A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732453 | |||||||
| chr5:74732475 | TAAAAAGA others(8): Show |
T | 1 | a0001c0001t0001g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1587+532_1587+546d others(17): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732475 | |||||||
| chr5:74732495 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1587+527A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732495 | |||||||
| chr5:74732602 | T | C | 6 | a0004c0007t0001g0039 a0004c0007t0001g0268 a0004c0007t0001g0269 others(3): Show |
7 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+420A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732602 | |||||||
| chr5:74732891 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1587+131T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732891 | |||||||
| chr5:74732927 | G | GAC | 31 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0030 others(28): Show |
41 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1587+93_1587+94dup others(2): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | |||||||
| chr5:74732927 | G | GACAC | 25 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(22): Show |
29 | HG00408.hp2 HG01257.hp2 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.1587+91_1587+94dup others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | |||||||
| chr5:74732927 | G | GACACAC | 13 | a0001c0001t0001g0034 a0001c0001t0001g0207 a0001c0001t0001g0212 others(10): Show |
14 | HG01346.hp1 HG01934.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1587+89_1587+94dup others(6): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | |||||||
| chr5:74732927 | G | GACACACA others(3): Show |
1 | a0001c0001t0001g0035 | 2 | HG00673.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1587+85_1587+94dup others(10): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | |||||||
| chr5:74732927 | GAC | G | 19 | a0001c0001t0001g0024 a0001c0001t0001g0031 a0001c0001t0001g0096 others(16): Show |
21 | HG00558.hp2 HG01243.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.1587+93_1587+94del others(2): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | |||||||
| chr5:74732927 | GACAC | G | 64 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0023 others(61): Show |
76 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1587+91_1587+94del others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | |||||||
| chr5:74732927 | GACACAC | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(58): Show |
81 | HG00140.hp2 HG00621.hp2 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.1587+89_1587+94del others(6): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | |||||||
| chr5:74732927 | GACACACA others(1): Show |
G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0090 a0001c0001t0001g0103 others(15): Show |
21 | HG01081.hp2 HG01106.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1587+87_1587+94del others(8): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | |||||||
| chr5:74732927 | GACACACA others(3): Show |
G | 22 | a0001c0001t0001g0026 a0001c0001t0001g0123 a0001c0001t0001g0294 others(19): Show |
24 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1587+85_1587+94del others(10): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | |||||||
| chr5:74732927 | GACACACA others(5): Show |
G | 15 | a0001c0001t0001g0166 a0001c0001t0001g0196 a0001c0001t0001g0211 others(12): Show |
17 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1587+83_1587+94del others(12): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | |||||||
| chr5:74732927 | GACACACA others(7): Show |
G | 2 | a0001c0001t0001g0104 a0002c0002t0001g0147 |
2 | HG02965.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1587+81_1587+94del others(14): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | |||||||
| chr5:74732927 | GACACACA others(13): Show |
G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0001g0102 others(6): Show |
12 | HG00609.hp1 HG00733.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1587+75_1587+94del others(20): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | |||||||
| chr5:74732978 | A | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0001g0102 others(4): Show |
9 | HG00609.hp1 HG02165.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1587+44T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732978 | |||||||
| chr5:74733229 | G | T | 1 | a0002c0008t0001g0171 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1511-131C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733229 | |||||||
| chr5:74733335 | G | GA | 76 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(73): Show |
88 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1511-238dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733335 | |||||||
| chr5:74733335 | GA | G | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-238delT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733335 | |||||||
| chr5:74733388 | G | A | 1 | a0002c0002t0002g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1511-290C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733388 | |||||||
| chr5:74733511 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1511-413G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733511 | |||||||
| chr5:74733517 | G | A | 1 | a0002c0002t0001g0153 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1511-419C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733517 | |||||||
| chr5:74733727 | T | C | 1 | a0003c0003t0001g0276 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1511-629A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733727 | |||||||
| chr5:74733761 | A | T | 85 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(82): Show |
98 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1511-663T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733761 | |||||||
| chr5:74733973 | C | CCT | 2 | a0001c0001t0001g0025 a0001c0001t0001g0234 |
3 | HG01891.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1511-877_1511-876d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733973 | |||||||
| chr5:74734243 | G | A | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-1145C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74734243 | |||||||
| chr5:74734256 | T | C | 73 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(70): Show |
84 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1511-1158A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74734256 | |||||||
| chr5:74734513 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(43): Show |
54 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1511-1415C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74734513 | |||||||
| chr5:74734540 | TC | T | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-1443delG | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74734540 | |||||||
| chr5:74734965 | C | T | 1 | a0001c0001t0003g0250 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1510+1831G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74734965 | |||||||
| chr5:74735194 | A | T | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1510+1602T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735194 | |||||||
| chr5:74735316 | T | C | 2 | a0002c0005t0001g0243 a0002c0005t0001g0244 |
2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1510+1480A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735316 | |||||||
| chr5:74735490 | G | C | 1 | a0002c0002t0002g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1510+1306C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735490 | |||||||
| chr5:74735553 | G | A | 1 | a0004c0012t0001g0281 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1510+1243C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735553 | |||||||
| chr5:74735700 | G | A | 32 | a0002c0005t0001g0302 a0003c0003t0001g0008 a0003c0003t0001g0013 others(29): Show |
42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1510+1096C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735700 | |||||||
| chr5:74735739 | A | G | 1 | a0002c0002t0001g0241 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1510+1057T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735739 | |||||||
| chr5:74735871 | T | C | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1510+925A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735871 | |||||||
| chr5:74736189 | G | C | 4 | a0001c0001t0001g0253 a0001c0001t0003g0037 a0001c0001t0003g0246 others(1): Show |
5 | HG03654.hp2 NA18965.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510+607C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74736189 | |||||||
| chr5:74736191 | A | T | 1 | a0001c0001t0001g0110 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1510+605T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74736191 | |||||||
| chr5:74736205 | G | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18982.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1510+591C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74736205 | |||||||
| chr5:74736274 | C | A | 1 | a0002c0002t0002g0069 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1510+522G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74736274 | |||||||
| chr5:74736291 | G | A | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1510+505C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74736291 | |||||||
| chr5:74736733 | T | C | 1 | a0001c0001t0003g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1510+63A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74736733 | |||||||
| chr5:74737043 | C | T | 3 | a0002c0002t0001g0174 a0002c0002t0001g0232 a0002c0002t0001g0236 |
3 | HG03041.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1321-58G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737043 | |||||||
| chr5:74737072 | T | C | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1321-87A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737072 | |||||||
| chr5:74737484 | T | C | 48 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0002g0002 others(45): Show |
57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1321-499A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737484 | |||||||
| chr5:74737592 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1321-607A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737592 | |||||||
| chr5:74737739 | G | C | 1 | a0003c0003t0001g0279 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1320+579C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737739 | |||||||
| chr5:74737833 | A | G | 5 | a0002c0008t0001g0135 a0002c0008t0001g0170 a0002c0008t0001g0171 others(2): Show |
5 | HG00438.hp2 HG00735.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1320+485T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737833 | |||||||
| chr5:74737872 | G | A | 1 | a0002c0002t0002g0070 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1320+446C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737872 | |||||||
| chr5:74737876 | G | A | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1320+442C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737876 | |||||||
| chr5:74738038 | A | G | 17 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0030 others(14): Show |
20 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1320+280T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74738038 | |||||||
| chr5:74738119 | C | T | 130 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(127): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1320+199G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74738119 | |||||||
| chr5:74738207 | C | A | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1320+111G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74738207 | |||||||
| chr5:74738420 | G | A | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
splice_region_variant&intron_variant | LOW | c.1221-3C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 13/20 | chr5 | 74738420 | |||||||
| chr5:74738750 | T | C | 2 | a0004c0009t0001g0154 a0004c0009t0001g0155 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1080-108A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738750 | |||||||
| chr5:74738760 | AAAT | A | 3 | a0002c0002t0001g0174 a0002c0002t0001g0232 a0002c0002t0001g0236 |
3 | HG03041.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1080-121_1080-119d others(5): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738760 | |||||||
| chr5:74738778 | G | A | 1 | a0001c0001t0003g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1080-136C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738778 | |||||||
| chr5:74738810 | A | T | 1 | a0002c0002t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1080-168T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738810 | |||||||
| chr5:74738945 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1080-303A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738945 | |||||||
| chr5:74738998 | C | T | 1 | a0003c0003t0001g0286 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1080-356G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738998 | |||||||
| chr5:74738999 | G | C | 5 | a0002c0008t0001g0135 a0002c0008t0001g0170 a0002c0008t0001g0171 others(2): Show |
5 | HG00438.hp2 HG00735.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1080-357C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738999 | |||||||
| chr5:74739155 | T | TGC | 3 | a0002c0002t0001g0174 a0002c0002t0001g0232 a0002c0002t0001g0236 |
3 | HG03041.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1080-515_1080-514d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739155 | |||||||
| chr5:74739158 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1080-516C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739158 | |||||||
| chr5:74739160 | A | C | 25 | a0002c0002t0001g0020 a0002c0002t0001g0134 a0002c0002t0001g0147 others(22): Show |
27 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1080-518T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739160 | |||||||
| chr5:74739369 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1079+620C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739369 | |||||||
| chr5:74739396 | G | A | 1 | a0002c0002t0002g0071 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1079+593C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739396 | |||||||
| chr5:74739460 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1079+529T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739460 | |||||||
| chr5:74739483 | T | C | 6 | a0004c0007t0001g0039 a0004c0007t0001g0268 a0004c0007t0001g0269 others(3): Show |
7 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079+506A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739483 | |||||||
| chr5:74739848 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG00621.hp1 HG02080.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1079+141G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739848 | |||||||
| chr5:74739970 | T | A | 1 | a0002c0002t0002g0072 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1079+19A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739970 | |||||||
| chr5:74740204 | G | T | 6 | a0002c0002t0001g0237 a0002c0002t0001g0238 a0002c0002t0001g0239 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-67C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740204 | |||||||
| chr5:74740256 | A | C | 1 | a0001c0001t0003g0263 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.931-119T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740256 | |||||||
| chr5:74740330 | C | T | 2 | a0003c0003t0001g0275 a0003c0003t0001g0276 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.931-193G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740330 | |||||||
| chr5:74740338 | T | C | 1 | a0001c0001t0003g0265 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.931-201A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740338 | |||||||
| chr5:74740423 | A | G | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.931-286T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740423 | |||||||
| chr5:74740575 | A | C | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.931-438T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740575 | |||||||
| chr5:74740948 | A | T | 11 | a0002c0002t0001g0020 a0002c0002t0001g0134 a0002c0002t0001g0147 others(8): Show |
13 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.930+581T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740948 | |||||||
| chr5:74740969 | A | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0026 others(13): Show |
24 | HG00323.hp1 HG00733.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.930+560T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740969 | |||||||
| chr5:74741176 | C | A | 1 | a0001c0001t0003g0250 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.930+353G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74741176 | |||||||
| chr5:74741178 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.930+351A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74741178 | |||||||
| chr5:74741680 | A | G | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.850-71T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74741680 | |||||||
| chr5:74741814 | G | A | 3 | a0002c0002t0001g0020 a0002c0002t0001g0150 a0002c0002t0001g0151 |
4 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-205C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74741814 | |||||||
| chr5:74742021 | C | T | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.850-412G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742021 | |||||||
| chr5:74742164 | C | T | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.850-555G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742164 | |||||||
| chr5:74742257 | T | TA | 45 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0093 others(42): Show |
58 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.850-649dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742257 | |||||||
| chr5:74742267 | A | C | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.850-658T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742267 | |||||||
| chr5:74742272 | C | A | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.850-663G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742272 | |||||||
| chr5:74742361 | G | C | 4 | a0002c0008t0001g0135 a0002c0008t0001g0171 a0002c0008t0001g0173 others(1): Show |
4 | HG00438.hp2 HG02293.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-752C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742361 | |||||||
| chr5:74742672 | C | CT | 52 | a0002c0002t0001g0020 a0002c0002t0001g0134 a0002c0002t0001g0147 others(49): Show |
63 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.850-1064dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742672 | |||||||
| chr5:74742980 | C | A | 25 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(22): Show |
34 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.850-1371G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742980 | |||||||
| chr5:74743050 | A | G | 1 | a0002c0005t0001g0304 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.850-1441T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743050 | |||||||
| chr5:74743141 | A | T | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.850-1532T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743141 | |||||||
| chr5:74743325 | C | A | 76 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(73): Show |
87 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.850-1716G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743325 | |||||||
| chr5:74743347 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.850-1738C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743347 | |||||||
| chr5:74743354 | C | A | 1 | a0002c0002t0001g0152 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.850-1745G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743354 | |||||||
| chr5:74743438 | C | T | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.850-1829G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743438 | |||||||
| chr5:74743559 | T | A | 1 | a0002c0006t0001g0143 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-1950A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743559 | |||||||
| chr5:74743588 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.850-1979C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743588 | |||||||
| chr5:74743636 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0234 |
3 | HG01891.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.850-2027A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743636 | |||||||
| chr5:74743856 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0211 |
2 | HG01981.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.849+1822C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743856 | |||||||
| chr5:74744017 | T | C | 2 | a0001c0001t0001g0213 a0001c0001t0001g0216 |
2 | HG02015.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.849+1661A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744017 | |||||||
| chr5:74744043 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.849+1635C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744043 | |||||||
| chr5:74744184 | CCATACAG others(4): Show |
C | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.849+1483_849+1493d others(13): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744184 | |||||||
| chr5:74744196 | T | A | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.849+1482A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744196 | |||||||
| chr5:74744362 | TA | T | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.849+1315delT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744362 | |||||||
| chr5:74744393 | G | GA | 48 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0002g0002 others(45): Show |
57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.849+1284dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744393 | |||||||
| chr5:74744615 | T | C | 2 | a0002c0002t0001g0232 a0002c0002t0001g0236 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.849+1063A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744615 | |||||||
| chr5:74744686 | A | C | 1 | a0002c0002t0001g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.849+992T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744686 | |||||||
| chr5:74744782 | T | C | 3 | a0001c0001t0001g0212 a0002c0005t0001g0230 a0002c0005t0001g0231 |
3 | HG01891.hp1 HG02129.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.849+896A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744782 | |||||||
| chr5:74744791 | T | A | 1 | a0001c0001t0001g0187 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.849+887A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744791 | |||||||
| chr5:74744927 | A | G | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.849+751T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744927 | |||||||
| chr5:74745054 | T | C | 1 | a0004c0007t0001g0272 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.849+624A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745054 | |||||||
| chr5:74745057 | G | A | 27 | a0001c0001t0001g0253 a0001c0001t0003g0007 a0001c0001t0003g0037 others(24): Show |
35 | HG00673.hp1 HG00741.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+621C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745057 | |||||||
| chr5:74745136 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.849+542C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745136 | |||||||
| chr5:74745280 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.849+398C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745280 | |||||||
| chr5:74745299 | T | C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(239): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.849+379A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745299 | |||||||
| chr5:74745440 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.849+238C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745440 | |||||||
| chr5:74745481 | A | G | 6 | a0004c0007t0001g0039 a0004c0007t0001g0268 a0004c0007t0001g0269 others(3): Show |
7 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.849+197T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745481 | |||||||
| chr5:74745504 | C | G | 32 | a0001c0001t0001g0100 a0003c0003t0001g0008 a0003c0003t0001g0013 others(29): Show |
42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.849+174G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745504 | |||||||
| chr5:74745961 | A | AT | 32 | a0001c0001t0001g0100 a0003c0003t0001g0008 a0003c0003t0001g0013 others(29): Show |
42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.670-105dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 9/20 | chr5 | 74745961 | |||||||
| chr5:74746175 | G | A | 1 | a0006c0010t0001g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.609-10C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746175 | |||||||
| chr5:74746301 | C | A | 1 | a0002c0002t0002g0081 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.609-136G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746301 | |||||||
| chr5:74746399 | T | TA | 3 | a0002c0002t0002g0043 a0002c0002t0002g0074 a0002c0002t0002g0076 |
3 | NA18949.hp1 NA18974.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.609-235dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746399 | |||||||
| chr5:74746403 | G | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0157 a0001c0001t0001g0158 |
4 | HG02809.hp2 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-238C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746403 | |||||||
| chr5:74746418 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.609-253C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746418 | |||||||
| chr5:74746451 | A | G | 1 | a0004c0007t0001g0270 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.609-286T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746451 | |||||||
| chr5:74746500 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0029 |
4 | NA18955.hp1 NA19003.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-335T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746500 | |||||||
| chr5:74746507 | A | T | 1 | a0002c0002t0002g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.609-342T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746507 | |||||||
| chr5:74746624 | T | C | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.609-459A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746624 | |||||||
| chr5:74746961 | T | C | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.608+731A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746961 | |||||||
| chr5:74746987 | T | C | 1 | a0001c0001t0003g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.608+705A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746987 | |||||||
| chr5:74747067 | C | G | 1 | a0004c0007t0001g0269 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.608+625G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747067 | |||||||
| chr5:74747138 | C | T | 1 | a0009c0016t0002g0055 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.608+554G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747138 | |||||||
| chr5:74747220 | G | C | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.608+472C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747220 | |||||||
| chr5:74747252 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0117 |
2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.608+440C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747252 | |||||||
| chr5:74747356 | G | A | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.608+336C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747356 | |||||||
| chr5:74747361 | A | G | 1 | a0002c0002t0002g0043 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.608+331T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747361 | |||||||
| chr5:74747575 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.608+117A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747575 | |||||||
| chr5:74747813 | G | C | 2 | a0002c0002t0002g0075 a0002c0002t0002g0079 |
2 | HG01109.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.520-33C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74747813 | |||||||
| chr5:74747958 | C | T | 6 | a0004c0007t0001g0039 a0004c0007t0001g0268 a0004c0007t0001g0269 others(3): Show |
7 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-178G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74747958 | |||||||
| chr5:74748109 | C | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(234): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.520-329G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748109 | |||||||
| chr5:74748332 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.520-552A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748332 | |||||||
| chr5:74748607 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.520-827C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748607 | |||||||
| chr5:74748780 | G | A | 26 | a0001c0001t0001g0100 a0003c0003t0001g0008 a0003c0003t0001g0013 others(23): Show |
35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.520-1000C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748780 | |||||||
| chr5:74748784 | G | A | 76 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(73): Show |
87 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.520-1004C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748784 | |||||||
| chr5:74748843 | C | A | 8 | a0003c0003t0001g0014 a0003c0003t0001g0273 a0003c0003t0001g0274 others(5): Show |
10 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.520-1063G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748843 | |||||||
| chr5:74748890 | T | TAAATA | 67 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0152 others(64): Show |
76 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.520-1115_520-1111d others(7): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748890 | |||||||
| chr5:74748890 | T | TAAATAAA others(3): Show |
9 | a0002c0002t0001g0232 a0002c0005t0001g0036 a0002c0005t0001g0042 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.520-1120_520-1111d others(12): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748890 | |||||||
| chr5:74748890 | T | TAAATAAA others(8): Show |
1 | a0002c0005t0001g0244 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.520-1125_520-1111d others(17): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748890 | |||||||
| chr5:74748909 | TAAA | T | 14 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0137 others(11): Show |
14 | HG00642.hp2 HG01361.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.520-1132_520-1130d others(5): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748909 | |||||||
| chr5:74748909 | TAAAAA | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0019 others(20): Show |
30 | HG00609.hp1 HG01074.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.520-1134_520-1130d others(7): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748909 | |||||||
| chr5:74748912 | A | AAT | 22 | a0001c0001t0001g0100 a0003c0003t0001g0008 a0003c0003t0001g0013 others(19): Show |
31 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.520-1133_520-1132i others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748912 | |||||||
| chr5:74748914 | A | T | 92 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(89): Show |
106 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.520-1134T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748914 | |||||||
| chr5:74748917 | T | A | 7 | a0003c0003t0001g0289 a0004c0007t0001g0039 a0004c0007t0001g0268 others(4): Show |
8 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-1137A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748917 | |||||||
| chr5:74748917 | TA | T | 6 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-1138delT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748917 | |||||||
| chr5:74748919 | A | AAAT | 15 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(12): Show |
21 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.520-1140_520-1139i others(5): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748919 | |||||||
| chr5:74748919 | A | T | 7 | a0003c0003t0001g0289 a0004c0007t0001g0039 a0004c0007t0001g0268 others(4): Show |
8 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-1139T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748919 | |||||||
| chr5:74748922 | A | T | 11 | a0001c0001t0001g0100 a0003c0003t0001g0008 a0003c0003t0001g0040 others(8): Show |
12 | HG01243.hp2 HG01361.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.520-1142T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748922 | |||||||
| chr5:74748925 | A | T | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0137 others(9): Show |
12 | HG00642.hp2 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.520-1145T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748925 | |||||||
| chr5:74748926 | AT | A | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0137 others(9): Show |
12 | HG00642.hp2 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.520-1147delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748926 | |||||||
| chr5:74748927 | T | TA | 22 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(19): Show |
29 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.520-1148dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748927 | |||||||
| chr5:74748927 | T | TAAAAAAA others(2): Show |
9 | a0001c0001t0001g0100 a0003c0003t0001g0008 a0003c0003t0001g0040 others(6): Show |
10 | HG01243.hp2 HG02165.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.520-1148_520-1147i others(11): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748927 | |||||||
| chr5:74748938 | AAAAATAA others(8): Show |
A | 1 | a0001c0001t0001g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.520-1173_520-1159d others(17): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748938 | |||||||
| chr5:74748942 | AT | A | 11 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0137 others(8): Show |
11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.520-1163delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748942 | |||||||
| chr5:74748943 | T | A | 2 | a0003c0003t0001g0274 a0004c0012t0001g0281 |
2 | HG01361.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.520-1163A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748943 | |||||||
| chr5:74748943 | T | C | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.520-1163A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748943 | |||||||
| chr5:74748946 | A | T | 13 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0137 others(10): Show |
13 | HG01361.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-1166T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748946 | |||||||
| chr5:74748948 | T | A | 13 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0137 others(10): Show |
13 | HG01361.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-1168A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748948 | |||||||
| chr5:74748963 | TAAAGA | T | 5 | a0002c0002t0001g0237 a0002c0002t0001g0238 a0002c0002t0001g0239 others(2): Show |
5 | HG01884.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-1188_520-1184d others(7): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748963 | |||||||
| chr5:74749528 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.519+1051A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74749528 | |||||||
| chr5:74749731 | C | T | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+848G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74749731 | |||||||
| chr5:74749756 | T | C | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+823A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74749756 | |||||||
| chr5:74749815 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.519+764A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74749815 | |||||||
| chr5:74750398 | C | A | 1 | a0001c0001t0001g0028 | 2 | HG00323.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.519+181G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74750398 | |||||||
| chr5:74750694 | C | T | 1 | a0002c0002t0002g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.431-27G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 6/20 | chr5 | 74750694 | |||||||
| chr5:74750831 | A | G | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.431-164T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 6/20 | chr5 | 74750831 | |||||||
| chr5:74751057 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.430+311G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 6/20 | chr5 | 74751057 | |||||||
| chr5:74751611 | G | A | 25 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(22): Show |
34 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.305-118C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74751611 | |||||||
| chr5:74751867 | C | T | 76 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(73): Show |
87 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.305-374G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74751867 | |||||||
| chr5:74751956 | C | A | 1 | a0002c0002t0002g0076 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.305-463G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74751956 | |||||||
| chr5:74752138 | T | G | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.305-645A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752138 | |||||||
| chr5:74752296 | T | G | 11 | a0005c0004t0001g0260 a0005c0004t0003g0006 a0005c0004t0003g0247 others(8): Show |
14 | NA18943.hp2 NA18944.hp2 NA18962.hp1 others(11): Show |
intron_variant | MODIFIER | c.305-803A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752296 | |||||||
| chr5:74752311 | T | G | 1 | a0001c0001t0001g0295 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.305-818A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752311 | |||||||
| chr5:74752325 | C | A | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.305-832G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752325 | |||||||
| chr5:74752374 | T | C | 3 | a0002c0002t0002g0049 a0002c0002t0002g0077 a0002c0002t0002g0078 |
3 | HG02135.hp2 NA18952.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.305-881A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752374 | |||||||
| chr5:74752424 | C | T | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.305-931G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752424 | |||||||
| chr5:74752662 | C | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0095 a0001c0001t0001g0118 others(2): Show |
6 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.305-1169G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752662 | |||||||
| chr5:74753221 | C | G | 25 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(22): Show |
34 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.305-1728G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74753221 | |||||||
| chr5:74753273 | G | T | 1 | a0002c0002t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.305-1780C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74753273 | |||||||
| chr5:74753283 | T | C | 1 | a0002c0017t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.305-1790A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74753283 | |||||||
| chr5:74753371 | G | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0026 others(13): Show |
24 | HG00323.hp1 HG00733.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.305-1878C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74753371 | |||||||
| chr5:74753511 | T | C | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.305-2018A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74753511 | |||||||
| chr5:74753957 | T | TG | 76 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(73): Show |
87 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.305-2465dupC | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74753957 | |||||||
| chr5:74754115 | G | T | 1 | a0002c0006t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.305-2622C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754115 | |||||||
| chr5:74754206 | A | T | 1 | a0001c0001t0001g0220 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.305-2713T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754206 | |||||||
| chr5:74754208 | A | G | 1 | a0006c0010t0001g0233 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.305-2715T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754208 | |||||||
| chr5:74754305 | GA | G | 71 | a0001c0001t0001g0183 a0002c0002t0001g0020 a0002c0002t0001g0134 others(68): Show |
85 | HG00280.hp2 HG00438.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.305-2813delT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754305 | |||||||
| chr5:74754305 | GAA | G | 47 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0002g0002 others(44): Show |
56 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.305-2814_305-2813d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754305 | |||||||
| chr5:74754319 | A | C | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.305-2826T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754319 | |||||||
| chr5:74754359 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.305-2866G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754359 | |||||||
| chr5:74754370 | A | G | 1 | a0002c0002t0002g0054 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.305-2877T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754370 | |||||||
| chr5:74754384 | G | T | 128 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(125): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.305-2891C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754384 | |||||||
| chr5:74754446 | G | A | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.305-2953C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754446 | |||||||
| chr5:74754490 | A | C | 129 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(126): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.305-2997T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754490 | |||||||
| chr5:74754490 | A | G | 1 | a0002c0005t0001g0303 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.305-2997T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754490 | |||||||
| chr5:74754602 | T | TA | 23 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(20): Show |
32 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.305-3110dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754602 | |||||||
| chr5:74754615 | G | A | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.305-3122C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754615 | |||||||
| chr5:74754662 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0298 |
2 | HG00609.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.305-3169G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754662 | |||||||
| chr5:74754927 | C | T | 85 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(82): Show |
98 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.305-3434G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754927 | |||||||
| chr5:74754955 | G | A | 4 | a0002c0002t0002g0017 a0002c0002t0002g0050 a0002c0002t0002g0080 others(1): Show |
5 | NA18953.hp2 NA18975.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-3462C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754955 | |||||||
| chr5:74755018 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.305-3525G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755018 | |||||||
| chr5:74755020 | C | T | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.305-3527G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755020 | |||||||
| chr5:74755075 | G | A | 1 | a0002c0002t0002g0051 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.305-3582C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755075 | |||||||
| chr5:74755302 | T | C | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.304+3547A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755302 | |||||||
| chr5:74755407 | T | A | 130 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(127): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.304+3442A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755407 | |||||||
| chr5:74755860 | A | C | 4 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0001g0298 others(1): Show |
4 | HG00609.hp2 HG00621.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+2989T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755860 | |||||||
| chr5:74755862 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.304+2987C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755862 | |||||||
| chr5:74755932 | C | T | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.304+2917G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755932 | |||||||
| chr5:74756031 | C | T | 5 | a0002c0008t0001g0135 a0002c0008t0001g0170 a0002c0008t0001g0171 others(2): Show |
5 | HG00438.hp2 HG00735.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+2818G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756031 | |||||||
| chr5:74756065 | C | G | 1 | a0004c0009t0001g0154 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.304+2784G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756065 | |||||||
| chr5:74756296 | CCA | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0026 others(13): Show |
24 | HG00323.hp1 HG00733.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.304+2551_304+2552d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756296 | |||||||
| chr5:74756595 | G | A | 4 | a0002c0008t0001g0135 a0002c0008t0001g0171 a0002c0008t0001g0173 others(1): Show |
4 | HG00438.hp2 HG02293.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.304+2254C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756595 | |||||||
| chr5:74756665 | G | GTA | 70 | a0001c0001t0001g0121 a0001c0001t0001g0218 a0002c0002t0001g0020 others(67): Show |
84 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.304+2182_304+2183d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756665 | |||||||
| chr5:74756670 | T | TAC | 48 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0002g0002 others(45): Show |
57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.304+2178_304+2179i others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756670 | |||||||
| chr5:74756681 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.304+2168T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756681 | |||||||
| chr5:74756808 | AG | A | 6 | a0002c0002t0001g0237 a0002c0002t0001g0238 a0002c0002t0001g0239 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.304+2040delC | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756808 | |||||||
| chr5:74756844 | T | C | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.304+2005A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756844 | |||||||
| chr5:74756949 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.304+1900C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756949 | |||||||
| chr5:74757340 | CT | C | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.304+1508delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757340 | |||||||
| chr5:74757702 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.304+1147G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757702 | |||||||
| chr5:74757730 | CTAAAA | C | 5 | a0002c0002t0001g0237 a0002c0002t0001g0239 a0002c0002t0001g0240 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+1114_304+1118d others(7): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757730 | |||||||
| chr5:74757731 | T | TA | 7 | a0001c0001t0001g0130 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG00621.hp1 HG01361.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.304+1117dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757731 | |||||||
| chr5:74757731 | TA | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(98): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.304+1117delT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757731 | |||||||
| chr5:74757731 | TAA | T | 6 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0226 others(3): Show |
6 | HG00642.hp2 HG01168.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.304+1116_304+1117d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757731 | |||||||
| chr5:74757731 | TAAAA | T | 34 | a0002c0002t0004g0067 a0002c0005t0001g0230 a0002c0005t0001g0231 others(31): Show |
43 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.304+1114_304+1117d others(6): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757731 | |||||||
| chr5:74757731 | TAAAAA | T | 88 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(85): Show |
101 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.304+1113_304+1117d others(7): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757731 | |||||||
| chr5:74757758 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.304+1091A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757758 | |||||||
| chr5:74757774 | G | A | 24 | a0002c0002t0001g0020 a0002c0002t0001g0134 a0002c0002t0001g0147 others(21): Show |
26 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.304+1075C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757774 | |||||||
| chr5:74757860 | C | T | 1 | a0001c0001t0003g0254 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.304+989G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757860 | |||||||
| chr5:74757919 | T | C | 5 | a0002c0002t0001g0134 a0002c0002t0001g0153 a0004c0009t0001g0021 others(2): Show |
6 | HG02451.hp1 HG02486.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.304+930A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757919 | |||||||
| chr5:74757939 | A | G | 130 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(127): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.304+910T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757939 | |||||||
| chr5:74758269 | T | C | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.304+580A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758269 | |||||||
| chr5:74758420 | T | C | 3 | a0001c0001t0003g0251 a0001c0001t0003g0254 a0001c0001t0003g0255 |
3 | HG02273.hp2 NA18953.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.304+429A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758420 | |||||||
| chr5:74758436 | T | G | 1 | a0001c0001t0001g0295 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.304+413A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758436 | |||||||
| chr5:74758569 | C | T | 1 | a0002c0002t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.304+280G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758569 | |||||||
| chr5:74758625 | C | T | 1 | a0005c0004t0003g0256 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.304+224G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758625 | |||||||
| chr5:74758629 | T | G | 1 | a0001c0001t0001g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304+220A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758629 | |||||||
| chr5:74758770 | A | G | 130 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(127): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.304+79T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758770 | |||||||
| chr5:74758816 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.304+33C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758816 | |||||||
| chr5:74758967 | AG | A | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.207-22delC | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74758967 | |||||||
| chr5:74759225 | G | A | 1 | a0002c0002t0001g0153 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.206+144C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759225 | |||||||
| chr5:74759251 | T | TAAAATTG others(55): Show |
1 | a0002c0006t0001g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.206+117_206+118ins others(62): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759251 | |||||||
| chr5:74759251 | T | TAAAATTG others(56): Show |
4 | a0002c0006t0001g0133 a0002c0006t0001g0138 a0002c0006t0001g0139 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.206+117_206+118ins others(63): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759251 | |||||||
| chr5:74759251 | T | TAAAATTG others(57): Show |
5 | a0002c0006t0001g0128 a0002c0006t0001g0136 a0002c0006t0001g0141 others(2): Show |
5 | HG02559.hp1 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.206+117_206+118ins others(64): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759251 | |||||||
| chr5:74759251 | T | TAAAATTG others(58): Show |
2 | a0002c0006t0001g0144 a0002c0019t0001g0145 |
2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.206+117_206+118ins others(65): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759251 | |||||||
| chr5:74759256 | T | C | 1 | a0003c0003t0001g0291 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.206+113A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759256 | |||||||
| chr5:74759297 | T | A | 1 | a0001c0001t0001g0220 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.206+72A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759297 | |||||||
| chr5:74759456 | T | C | 1 | a0002c0002t0002g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.149-30A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74759456 | |||||||
| chr5:74759593 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.149-167T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74759593 | |||||||
| chr5:74759862 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.149-436A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74759862 | |||||||
| chr5:74759914 | T | G | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.149-488A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74759914 | |||||||
| chr5:74760074 | AAGGCAGT others(9): Show |
A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.149-664_149-649del others(16): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760074 | |||||||
| chr5:74760105 | C | G | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.149-679G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760105 | |||||||
| chr5:74760197 | T | C | 1 | a0006c0010t0001g0221 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.148+705A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760197 | |||||||
| chr5:74760639 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.148+263A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760639 | |||||||
| chr5:74760659 | C | T | 8 | a0001c0001t0001g0253 a0001c0001t0003g0037 a0001c0001t0003g0245 others(5): Show |
9 | HG00673.hp1 HG02273.hp2 HG03654.hp2 others(6): Show |
intron_variant | MODIFIER | c.148+243G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760659 | |||||||
| chr5:74760688 | T | C | 36 | a0002c0008t0001g0135 a0002c0008t0001g0170 a0002c0008t0001g0171 others(33): Show |
46 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.148+214A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760688 | |||||||
| chr5:74760850 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0234 |
3 | HG01891.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.148+52T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760850 | |||||||
| chr5:74761262 | T | C | 1 | a0002c0002t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64-276A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74761262 | |||||||
| chr5:74761889 | G | A | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.64-903C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74761889 | |||||||
| chr5:74761973 | T | C | 3 | a0002c0002t0001g0174 a0002c0002t0001g0232 a0002c0002t0001g0236 |
3 | HG03041.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.64-987A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74761973 | |||||||
| chr5:74762012 | G | A | 2 | a0001c0001t0001g0222 a0003c0013t0001g0292 |
2 | HG01243.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.64-1026C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762012 | |||||||
| chr5:74762029 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.64-1043C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762029 | |||||||
| chr5:74762258 | C | T | 130 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(127): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.64-1272G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762258 | |||||||
| chr5:74762393 | T | C | 4 | a0002c0002t0002g0053 a0002c0002t0002g0082 a0002c0002t0002g0083 others(1): Show |
4 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1287A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762393 | |||||||
| chr5:74762435 | T | C | 130 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(127): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.63+1245A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762435 | |||||||
| chr5:74762524 | T | TACCATAG others(3): Show |
1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1155_63+1156ins others(10): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762524 | |||||||
| chr5:74762573 | G | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(208): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.63+1107C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762573 | |||||||
| chr5:74762628 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1052A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762628 | |||||||
| chr5:74762638 | C | CAACTTGC others(5): Show |
1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1041_63+1042ins others(12): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762638 | |||||||
| chr5:74762641 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1039A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762641 | |||||||
| chr5:74762644 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1036A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762644 | |||||||
| chr5:74762646 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1034A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762646 | |||||||
| chr5:74762649 | C | T | 1 | a0004c0007t0001g0268 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.63+1031G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762649 | |||||||
| chr5:74762650 | G | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0001g0102 others(4): Show |
9 | HG00609.hp1 HG02165.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+1030C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762650 | |||||||
| chr5:74762654 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1026A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762654 | |||||||
| chr5:74762656 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1024C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762656 | |||||||
| chr5:74762657 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1023C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762657 | |||||||
| chr5:74762660 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1020G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762660 | |||||||
| chr5:74762663 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1017C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762663 | |||||||
| chr5:74762665 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1015A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762665 | |||||||
| chr5:74762670 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1010A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762670 | |||||||
| chr5:74762675 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1005A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762675 | |||||||
| chr5:74762677 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1003T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762677 | |||||||
| chr5:74762751 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+929A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762751 | |||||||
| chr5:74762752 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+928C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762752 | |||||||
| chr5:74762767 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+913A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762767 | |||||||
| chr5:74762778 | T | C | 1 | a0002c0002t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.63+902A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762778 | |||||||
| chr5:74762788 | A | G | 130 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(127): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.63+892T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762788 | |||||||
| chr5:74762799 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+881A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762799 | |||||||
| chr5:74762805 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+875C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762805 | |||||||
| chr5:74762807 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+873C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762807 | |||||||
| chr5:74762808 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+872C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762808 | |||||||
| chr5:74762810 | ATTAAGTG others(4): Show |
A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+859_63+869delAT others(9): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762810 | |||||||
| chr5:74762822 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+858C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762822 | |||||||
| chr5:74762829 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+851C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762829 | |||||||
| chr5:74762861 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+819A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762861 | |||||||
| chr5:74762862 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+818A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762862 | |||||||
| chr5:74762863 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+817A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762863 | |||||||
| chr5:74762866 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+814T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762866 | |||||||
| chr5:74762869 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+811A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762869 | |||||||
| chr5:74762870 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+810A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762870 | |||||||
| chr5:74762871 | ATGAATTA others(25): Show |
A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+777_63+808delAA others(30): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762871 | |||||||
| chr5:74762906 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+774C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762906 | |||||||
| chr5:74762907 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+773T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762907 | |||||||
| chr5:74762910 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+770T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762910 | |||||||
| chr5:74762913 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+767C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762913 | |||||||
| chr5:74762914 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+766A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762914 | |||||||
| chr5:74762915 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+765A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762915 | |||||||
| chr5:74762916 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+764C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762916 | |||||||
| chr5:74762919 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+761A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762919 | |||||||
| chr5:74762921 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+759A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762921 | |||||||
| chr5:74762922 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+758C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762922 | |||||||
| chr5:74762924 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+756C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762924 | |||||||
| chr5:74762925 | C | CCCCCCCC others(37): Show |
1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+754_63+755insTG others(42): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762925 | |||||||
| chr5:74763022 | TTAAAG | T | 85 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0001g0020 others(82): Show |
98 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.63+653_63+657delCT others(3): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763022 | |||||||
| chr5:74763083 | T | A | 1 | a0001c0001t0001g0223 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.63+597A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763083 | |||||||
| chr5:74763155 | A | G | 1 | a0001c0001t0003g0251 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.63+525T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763155 | |||||||
| chr5:74763248 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.63+432A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763248 | |||||||
| chr5:74763266 | T | C | 34 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(31): Show |
42 | HG00673.hp1 HG00741.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.63+414A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763266 | |||||||
| chr5:74763269 | A | G | 2 | a0003c0003t0001g0273 a0003c0003t0001g0274 |
2 | HG00738.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.63+411T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763269 | |||||||
| chr5:74763550 | G | C | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+130C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763550 | |||||||
| chr5:74763802 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-24-36G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74763802 | |||||||
| chr5:74763883 | T | C | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-24-117A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74763883 | |||||||
| chr5:74763945 | T | A | 5 | a0002c0008t0001g0135 a0002c0008t0001g0170 a0002c0008t0001g0171 others(2): Show |
5 | HG00438.hp2 HG00735.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-179A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74763945 | |||||||
| chr5:74763990 | GT | G | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-24-225delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74763990 | |||||||
| chr5:74764001 | G | A | 1 | a0004c0012t0001g0293 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-24-235C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764001 | |||||||
| chr5:74764024 | C | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0096 a0001c0001t0001g0126 |
7 | HG01928.hp1 HG01943.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24-258G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764024 | |||||||
| chr5:74764026 | G | A | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-24-260C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764026 | |||||||
| chr5:74764343 | G | A | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24-577C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764343 | |||||||
| chr5:74764493 | T | C | 2 | a0002c0002t0001g0232 a0002c0002t0001g0236 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-24-727A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764493 | |||||||
| chr5:74764500 | T | A | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-24-734A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764500 | |||||||
| chr5:74764598 | T | C | 1 | a0006c0010t0001g0233 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-24-832A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764598 | |||||||
| chr5:74764632 | GTTA | G | 12 | a0002c0006t0001g0128 a0002c0006t0001g0133 a0002c0006t0001g0136 others(9): Show |
12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-24-869_-24-867del others(3): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764632 | |||||||
| chr5:74764657 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-24-891A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764657 | |||||||
| chr5:74764733 | C | T | 1 | a0002c0006t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-24-967G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764733 | |||||||
| chr5:74764778 | G | GT | 75 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(72): Show |
83 | HG00558.hp1 HG00621.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.-24-1013dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764778 | |||||||
| chr5:74764778 | G | GTT | 9 | a0002c0002t0001g0134 a0002c0002t0001g0237 a0002c0002t0001g0238 others(6): Show |
9 | HG00438.hp2 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-24-1014_-24-1013d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764778 | |||||||
| chr5:74764778 | GT | G | 29 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0234 others(26): Show |
38 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.-24-1013delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764778 | |||||||
| chr5:74764807 | AC | A | 6 | a0002c0002t0001g0237 a0002c0002t0001g0238 a0002c0002t0001g0239 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24-1042delG | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764807 | |||||||
| chr5:74765017 | C | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG00621.hp1 HG02080.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.-24-1251G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765017 | |||||||
| chr5:74765175 | CTTT | C | 9 | a0002c0005t0001g0036 a0002c0005t0001g0042 a0002c0005t0001g0243 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-24-1412_-24-1410d others(5): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765175 | |||||||
| chr5:74765256 | T | G | 27 | a0001c0001t0001g0253 a0001c0001t0003g0007 a0001c0001t0003g0037 others(24): Show |
35 | HG00673.hp1 HG00741.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-24-1490A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765256 | |||||||
| chr5:74765371 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-25+1567T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765371 | |||||||
| chr5:74765419 | T | C | 25 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(22): Show |
34 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.-25+1519A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765419 | |||||||
| chr5:74765456 | G | A | 31 | a0003c0003t0001g0008 a0003c0003t0001g0013 a0003c0003t0001g0014 others(28): Show |
41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-25+1482C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765456 | |||||||
| chr5:74765588 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-25+1350C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765588 | |||||||
| chr5:74765640 | C | T | 1 | a0002c0006t0001g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-25+1298G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765640 | |||||||
| chr5:74765692 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-25+1246C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765692 | |||||||
| chr5:74765763 | G | A | 1 | a0002c0002t0001g0296 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25+1175C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765763 | |||||||
| chr5:74766245 | G | C | 1 | a0002c0002t0002g0085 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-25+693C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766245 | |||||||
| chr5:74766370 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-25+568T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766370 | |||||||
| chr5:74766417 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01257.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-25+521G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766417 | |||||||
| chr5:74766441 | G | C | 48 | a0001c0011t0002g0044 a0001c0011t0002g0073 a0002c0002t0002g0002 others(45): Show |
57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-25+497C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766441 | |||||||
| chr5:74766499 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-25+439G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766499 | |||||||
| chr5:74766533 | G | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(44): Show |
55 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.-25+405C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766533 | |||||||
| chr5:74766633 | T | TCTTCTTC others(11): Show |
1 | a0001c0001t0001g0297 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-25+287_-25+304dup others(18): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766633 | |||||||
| chr5:74766744 | G | C | 1 | a0001c0001t0001g0298 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-25+194C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766744 | |||||||
| chr5:74766771 | T | G | 1 | a0001c0001t0001g0299 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-25+167A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766771 | |||||||
| chr5:74766774 | T | C | 6 | a0002c0005t0001g0042 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
7 | HG02145.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25+164A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766774 |