Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 85476 |
| ensemblid | ENSG00000168827.15 |
| hgncid | 13780 |
| symbol | GFM1 |
| name | G elongation factor mitochondrial 1 |
| refseq_nuc | NM_024996.7 |
| refseq_prot | NP_079272.4 |
| ensembl_nuc | ENST00000486715.6 |
| ensembl_prot | ENSP00000419038.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 158644527 |
| end | 158695581 |
| strand | + |
| ver | v1.2 |
| region | chr3:158644527-158695581 |
| region5000 | chr3:158639527-158700581 |
| regionname0 | GFM1_chr3_158644527_158695581 |
| regionname5000 | GFM1_chr3_158639527_158700581 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 751 | 219 | 68 | 32 | 88 | 11 | 20 | 71 | GFM1_chr3_158639527_158700581 | GFM1 | MRLLG others(746): Show |
chr3 | 158639527 | 158700581 |
| a0002 | 1/1 | 751 | 136 | 13 | 27 | 70 | 7 | 17 | 56 | GFM1_chr3_158639527_158700581 | GFM1 | MRLLG others(746): Show |
chr3 | 158639527 | 158700581 |
| a0003 | 0/0 | 751 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | MRLLG others(746): Show |
chr3 | 158639527 | 158700581 |
| a0004 | 0/0 | 751 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | GFM1_chr3_158639527_158700581 | GFM1 | MRLLG others(746): Show |
chr3 | 158639527 | 158700581 |
| a0005 | 0/0 | 751 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | MRLLG others(746): Show |
chr3 | 158639527 | 158700581 |
| a0006 | 0/0 | 751 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | MRLLG others(746): Show |
chr3 | 158639527 | 158700581 |
| a0007 | 0/0 | 751 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | MRLLG others(746): Show |
chr3 | 158639527 | 158700581 |
| a0008 | 0/0 | 751 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | MRLLG others(746): Show |
chr3 | 158639527 | 158700581 |
| a0009 | 0/0 | 38 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | MRLLG others(33): Show |
chr3 | 158639527 | 158700581 |
| a0010 | 0/0 | 751 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | MRLLG others(746): Show |
chr3 | 158639527 | 158700581 |
| a0011 | 0/0 | 751 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | MRLLG others(746): Show |
chr3 | 158639527 | 158700581 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2253 | 214 | 65 | 31 | 87 | 11 | 20 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0001c0004 | 0/0 | 2253 | 3 | 1 | 1 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0001c0008 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0001c0009 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0002c0002 | 1/1 | 2253 | 135 | 13 | 27 | 69 | 7 | 17 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0002c0013 | 0/0 | 2253 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0003c0003 | 0/0 | 2253 | 7 | 6 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0004c0005 | 0/0 | 2253 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0005c0015 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0006c0007 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0007c0012 | 0/0 | 2253 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0008c0011 | 0/0 | 2253 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0009c0006 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2237): Show |
chr3 | 158639527 | 158700581 | ||
| a0010c0014 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 | ||
| a0011c0010 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | ATGAG others(2248): Show |
chr3 | 158639527 | 158700581 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 6478 | 54 | 4 | 8 | 32 | 4 | 6 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0003 | 0/0 | 6474 | 52 | 8 | 10 | 28 | 3 | 3 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6469): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0004 | 0/0 | 6478 | 51 | 18 | 10 | 12 | 4 | 7 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0005 | 0/0 | 6476 | 9 | 9 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6471): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0006 | 0/0 | 6478 | 9 | 0 | 0 | 9 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0007 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0008 | 0/0 | 6478 | 5 | 5 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0009 | 0/0 | 6478 | 5 | 5 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0011 | 0/0 | 6478 | 3 | 3 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0013 | 0/0 | 6478 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0014 | 0/0 | 6478 | 3 | 3 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0015 | 0/0 | 6478 | 2 | 0 | 0 | 0 | 0 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0016 | 0/0 | 6478 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0017 | 0/0 | 6478 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0018 | 0/0 | 6478 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0020 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0021 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0022 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0023 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0027 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0028 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0030 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0031 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0032 | 0/0 | 6474 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6469): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0034 | 0/0 | 6474 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6469): Show |
chr3 | 158639527 | 158700581 |
| a0001c0001t0036 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0004t0024 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0004t0025 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0004t0026 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0008t0008 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0001c0009t0029 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0002c0002t0001 | 0/1 | 6478 | 126 | 13 | 25 | 65 | 6 | 16 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0002c0002t0010 | 1/0 | 6478 | 4 | 0 | 2 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0002c0002t0012 | 0/0 | 6478 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0002c0002t0019 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0002c0002t0035 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0002c0013t0001 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0003c0003t0007 | 0/0 | 6478 | 7 | 6 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0004c0005t0003 | 0/0 | 6474 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6469): Show |
chr3 | 158639527 | 158700581 |
| a0004c0005t0033 | 0/0 | 6474 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6469): Show |
chr3 | 158639527 | 158700581 |
| a0005c0015t0001 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0006c0007t0002 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0007c0012t0001 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0008c0011t0004 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0009c0006t0011 | 0/0 | 6467 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6462): Show |
chr3 | 158639527 | 158700581 |
| a0010c0014t0001 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| a0011c0010t0002 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | GCTCT others(6473): Show |
chr3 | 158639527 | 158700581 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 6 | 1 | 3 | 1 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0009 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0002 | 0/0 | 7 | 0 | 4 | 2 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0014 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0006g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0008g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0009g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0009g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0009g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0011g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0011g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0011g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0013g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0013g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0013g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0014g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0014g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0014g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0015g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0016g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0017g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0018g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0018g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0020g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0022g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0023g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0027g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0028g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0030g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0031g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0032g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0034g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0001t0036g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0004t0024g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0004t0025g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0004t0026g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0008t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0001c0009t0029g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0003 | 0/0 | 5 | 2 | 0 | 2 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0004 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0007 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0010g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0010g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0010g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0010g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0012g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0012g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0012g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0019g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0002t0035g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0002c0013t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0003c0003t0007g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0003c0003t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0003c0003t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0003c0003t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0003c0003t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0003c0003t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0003c0003t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0004c0005t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0004c0005t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0004c0005t0033g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0005c0015t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0006c0007t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0007c0012t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0008c0011t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0009c0006t0011g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0010c0014t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| a0011c0010t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0010 | g0130 | EUR | GBR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0058 | EUR | GBR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | GBR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | GBR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0052 | EUR | FIN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0220 | EUR | FIN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | FIN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0007 | EUR | FIN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0107 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0109 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0260 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0242 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0282 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01109 | hp1 | a0005 | c0015 | t0001 | g0140 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01109 | hp2 | a0006 | c0007 | t0002 | g0056 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01175 | hp1 | a0003 | c0003 | t0007 | g0230 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01243 | hp1 | a0001 | c0004 | t0026 | g0305 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01243 | hp2 | a0001 | c0001 | t0028 | g0264 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0265 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01261 | hp1 | a0002 | c0002 | t0010 | g0122 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01433 | hp2 | a0001 | c0001 | t0027 | g0236 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0026 | EUR | IBS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0132 | EUR | IBS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0274 | EUR | IBS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0203 | EUR | IBS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0243 | EUR | IBS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | IBS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0293 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0267 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0227 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01943 | hp2 | a0002 | c0002 | t0010 | g0131 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02040 | hp1 | a0001 | c0001 | t0021 | g0001 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02040 | hp2 | a0007 | c0012 | t0001 | g0008 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02055 | hp1 | a0001 | c0001 | t0011 | g0228 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0096 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0287 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | CDX | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CDX | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0291 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0281 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02300 | hp2 | a0001 | c0001 | t0034 | g0182 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02572 | hp2 | a0003 | c0003 | t0007 | g0235 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0143 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02602 | hp2 | a0008 | c0011 | t0004 | g0299 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02622 | hp1 | a0009 | c0006 | t0011 | g0298 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02622 | hp2 | a0001 | c0001 | t0036 | g0288 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02630 | hp2 | a0003 | c0003 | t0007 | g0261 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0262 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02647 | hp2 | a0001 | c0004 | t0025 | g0300 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0266 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0258 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0118 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0104 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0294 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0123 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0238 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0125 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02809 | hp2 | a0003 | c0003 | t0007 | g0250 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0292 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02818 | hp2 | a0003 | c0003 | t0007 | g0248 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0271 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0277 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02895 | hp1 | a0001 | c0001 | t0017 | g0028 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0129 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0105 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0270 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0303 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02970 | hp2 | a0010 | c0014 | t0001 | g0094 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0086 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0126 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0296 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03130 | hp1 | a0001 | c0001 | t0017 | g0028 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03139 | hp2 | a0001 | c0001 | t0018 | g0304 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0256 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03195 | hp2 | a0001 | c0009 | t0029 | g0295 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0289 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0269 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03225 | hp2 | a0001 | c0001 | t0023 | g0306 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0290 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03486 | hp1 | a0001 | c0001 | t0030 | g0224 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03486 | hp2 | a0001 | c0001 | t0014 | g0178 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03490 | hp1 | a0001 | c0001 | t0015 | g0016 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0145 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0146 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03492 | hp2 | a0001 | c0001 | t0015 | g0016 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03516 | hp1 | a0011 | c0010 | t0002 | g0090 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0279 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0272 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0030 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03831 | hp1 | a0001 | c0001 | t0031 | g0037 | SAS | BEB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0215 | SAS | BEB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | BEB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03942 | hp2 | a0001 | c0001 | t0022 | g0033 | SAS | BEB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0124 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0013 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | YRI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18522 | hp2 | a0001 | c0001 | t0014 | g0179 | AFR | YRI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | CHB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18612 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | CHB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | CHB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0048 | AFR | YRI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0286 | AFR | YRI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18947 | hp1 | a0002 | c0013 | t0001 | g0101 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18947 | hp2 | a0001 | c0004 | t0024 | g0283 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18949 | hp1 | a0001 | c0001 | t0020 | g0064 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18953 | hp1 | a0001 | c0001 | t0013 | g0275 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18966 | hp2 | a0004 | c0005 | t0003 | g0185 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18971 | hp1 | a0001 | c0001 | t0032 | g0209 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18985 | hp2 | a0002 | c0002 | t0012 | g0082 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18987 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18988 | hp2 | a0001 | c0001 | t0006 | g0063 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18989 | hp2 | a0004 | c0005 | t0033 | g0009 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19004 | hp2 | a0001 | c0001 | t0013 | g0030 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | LWK | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19043 | hp2 | a0003 | c0003 | t0007 | g0247 | AFR | LWK | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19059 | hp1 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19060 | hp2 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19062 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19070 | hp2 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19075 | hp2 | a0002 | c0002 | t0012 | g0020 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19079 | hp2 | a0002 | c0002 | t0012 | g0150 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19084 | hp2 | a0002 | c0002 | t0019 | g0114 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19088 | hp2 | a0004 | c0005 | t0003 | g0181 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | YRI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | YRI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA20129 | hp1 | a0001 | c0008 | t0008 | g0249 | AFR | ASW | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ASW | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0241 | EUR | TSI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0137 | EUR | TSI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0149 | EUR | TSI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA20905 | hp1 | a0002 | c0002 | t0035 | g0010 | SAS | GIH | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | GIH | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0284 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0097 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02486 | hp1 | a0003 | c0003 | t0007 | g0254 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0229 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0245 | AFR | USA | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | USA | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA20300 | hp2 | a0001 | c0001 | t0016 | g0036 | AFR | USA | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | LWK | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | LWK | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0147 | REF | REF | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0010 | g0111 | REF | REF | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:158644711 | A | G | 1 | a0008 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.77A>G | p.Lys26Arg | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | 185/6478 | 77/2256 | 26/751 | chr3 | 158644711 | |||
| chr3:158645635 | TGGAAGGC others(4): Show |
T | 1 | a0009 | 1 | HG02622.hp1 | frameshift_variant | HIGH | c.89_99delGGAAGGCCTG others(1): Show |
p.Trp30fs | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 2/18 | 197/6478 | 89/2256 | 30/751 | chr3 | 158645635 | |||
| chr3:158645674 | A | G | 1 | a0005 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.127A>G | p.Asn43Asp | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 2/18 | 235/6478 | 127/2256 | 43/751 | chr3 | 158645674 | |||
| chr3:158646851 | A | G | 1 | a0003 | 7 | HG01175.hp1 HG02486.hp1 HG02572.hp2 others(4): Show |
missense_variant | MODERATE | c.476A>G | p.Asn159Ser | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/18 | 584/6478 | 476/2256 | 159/751 | chr3 | 158646851 | |||
| chr3:158646943 | A | C | 1 | a0011 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.568A>C | p.Met190Leu | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/18 | 676/6478 | 568/2256 | 190/751 | chr3 | 158646943 | |||
| chr3:158649064 | C | T | 1 | a0004 | 3 | NA18966.hp2 NA18989.hp2 NA19088.hp2 |
missense_variant | MODERATE | c.596C>T | p.Ala199Val | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/18 | 704/6478 | 596/2256 | 199/751 | chr3 | 158649064 | |||
| chr3:158649090 | G | A | 1 | a0007 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.622G>A | p.Glu208Lys | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/18 | 730/6478 | 622/2256 | 208/751 | chr3 | 158649090 | |||
| chr3:158649111 | G | A | 7 | a0001 a0003 a0004 others(4): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
missense_variant | MODERATE | c.643G>A | p.Val215Ile | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/18 | 751/6478 | 643/2256 | 215/751 | chr3 | 158649111 | |||
| chr3:158662647 | A | G | 1 | a0010 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1343A>G | p.Asp448Gly | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/18 | 1451/6478 | 1343/2256 | 448/751 | chr3 | 158662647 | |||
| chr3:158690264 | C | T | 1 | a0006 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.2011C>T | p.Arg671Cys | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/18 | 2119/6478 | 2011/2256 | 671/751 | chr3 | 158690264 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:158644652 | T | C | 10 | a0001c0001 a0001c0004 a0001c0008 others(7): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
synonymous_variant | LOW | c.18T>C | p.Ala6Ala | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | 126/6478 | 18/2256 | 6/751 | chr3 | 158644652 | |||
| chr3:158652111 | T | C | 1 | a0005c0015 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.705T>C | p.Tyr235Tyr | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/18 | 813/6478 | 705/2256 | 235/751 | chr3 | 158652111 | |||
| chr3:158659047 | C | T | 1 | a0001c0004 | 3 | HG01243.hp1 HG02647.hp2 NA18947.hp2 |
synonymous_variant | LOW | c.1209C>T | p.Ala403Ala | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/18 | 1317/6478 | 1209/2256 | 403/751 | chr3 | 158659047 | |||
| chr3:158666378 | C | T | 1 | a0001c0009 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1593C>T | p.Ala531Ala | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/18 | 1701/6478 | 1593/2256 | 531/751 | chr3 | 158666378 | |||
| chr3:158682103 | A | G | 1 | a0002c0013 | 1 | NA18947.hp1 | synonymous_variant | LOW | c.1710A>G | p.Ser570Ser | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/18 | 1818/6478 | 1710/2256 | 570/751 | chr3 | 158682103 | |||
| chr3:158684541 | C | T | 1 | a0001c0008 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.1782C>T | p.Cys594Cys | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/18 | 1890/6478 | 1782/2256 | 594/751 | chr3 | 158684541 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:158644562 | C | T | 3 | a0001c0001t0009 a0001c0001t0018 a0001c0001t0036 |
8 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-73C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | chr3 | 158644562 | |||||||
| chr3:158644569 | C | T | 1 | a0002c0002t0035 | 1 | NA20905.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-66C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | chr3 | 158644569 | |||||||
| chr3:158644602 | C | T | 5 | a0001c0001t0003 a0001c0001t0032 a0001c0001t0034 others(2): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-33C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | 33 | chr3 | 158644602 | ||||||
| chr3:158644604 | A | G | 2 | a0001c0001t0006 a0001c0001t0031 |
10 | HG00621.hp2 HG02155.hp1 HG03831.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-31A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | 31 | chr3 | 158644604 | ||||||
| chr3:158644624 | C | T | 2 | a0001c0001t0011 a0009c0006t0011 |
4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-11C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | chr3 | 158644624 | |||||||
| chr3:158691473 | C | T | 27 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(24): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*6C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 6 | chr3 | 158691473 | ||||||
| chr3:158691583 | C | T | 1 | a0001c0001t0030 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*116C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 116 | chr3 | 158691583 | ||||||
| chr3:158691693 | C | T | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(35): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*226C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 226 | chr3 | 158691693 | ||||||
| chr3:158691918 | TTTG | T | 5 | a0001c0001t0003 a0001c0001t0032 a0001c0001t0034 others(2): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*454_*456delGTT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 454 | INFO_REALIGN_3_PRIME | chr3 | 158691918 | |||||
| chr3:158691932 | T | C | 1 | a0001c0001t0020 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*465T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 465 | chr3 | 158691932 | ||||||
| chr3:158691950 | T | TTA | 1 | a0001c0001t0005 | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*483_*484insTA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 484 | chr3 | 158691950 | ||||||
| chr3:158692006 | C | T | 2 | a0001c0001t0017 a0001c0001t0030 |
3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*539C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 539 | chr3 | 158692006 | ||||||
| chr3:158692135 | T | A | 1 | a0001c0001t0021 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*668T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 668 | chr3 | 158692135 | ||||||
| chr3:158692158 | T | A | 27 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(24): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*691T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 691 | chr3 | 158692158 | ||||||
| chr3:158692180 | C | T | 5 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0018 others(2): Show |
12 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*713C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 713 | chr3 | 158692180 | ||||||
| chr3:158692233 | G | T | 2 | a0001c0001t0009 a0001c0001t0036 |
6 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*766G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 766 | chr3 | 158692233 | ||||||
| chr3:158692334 | G | C | 1 | a0001c0004t0024 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*867G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 867 | chr3 | 158692334 | ||||||
| chr3:158692335 | T | A | 1 | a0001c0004t0024 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*868T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 868 | chr3 | 158692335 | ||||||
| chr3:158692694 | T | A | 2 | a0001c0001t0008 a0001c0008t0008 |
6 | HG01884.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1227T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1227 | chr3 | 158692694 | ||||||
| chr3:158692724 | C | A | 1 | a0001c0001t0013 | 3 | NA18953.hp1 NA19004.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1257C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1257 | chr3 | 158692724 | ||||||
| chr3:158692819 | G | A | 1 | a0002c0002t0012 | 3 | NA18985.hp2 NA19075.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1352G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1352 | chr3 | 158692819 | ||||||
| chr3:158692840 | C | T | 1 | a0001c0001t0023 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1373C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1373 | chr3 | 158692840 | ||||||
| chr3:158693254 | A | T | 1 | a0002c0002t0019 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1787A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1787 | chr3 | 158693254 | ||||||
| chr3:158693263 | T | C | 1 | a0001c0004t0025 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1796T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1796 | chr3 | 158693263 | ||||||
| chr3:158693383 | A | G | 1 | a0001c0001t0028 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1916A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1916 | chr3 | 158693383 | ||||||
| chr3:158693612 | A | G | 1 | a0001c0001t0027 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2145A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2145 | chr3 | 158693612 | ||||||
| chr3:158693739 | T | G | 1 | a0001c0009t0029 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2272T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2272 | chr3 | 158693739 | ||||||
| chr3:158693742 | A | T | 1 | a0001c0001t0016 | 2 | NA18906.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2275A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2275 | chr3 | 158693742 | ||||||
| chr3:158693892 | C | T | 15 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(12): Show |
128 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2425C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2425 | chr3 | 158693892 | ||||||
| chr3:158693915 | G | A | 5 | a0001c0001t0003 a0001c0001t0032 a0001c0001t0034 others(2): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2448G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2448 | chr3 | 158693915 | ||||||
| chr3:158693942 | A | G | 2 | a0001c0001t0015 a0001c0001t0022 |
3 | HG03490.hp1 HG03492.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2475A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2475 | chr3 | 158693942 | ||||||
| chr3:158693957 | G | A | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(43): Show |
367 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(364): Show |
3_prime_UTR_variant | MODIFIER | c.*2490G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2490 | chr3 | 158693957 | ||||||
| chr3:158694016 | GT | G | 1 | a0001c0001t0005 | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2560delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2560 | INFO_REALIGN_3_PRIME | chr3 | 158694016 | |||||
| chr3:158694155 | A | G | 1 | a0001c0001t0036 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2688A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2688 | chr3 | 158694155 | ||||||
| chr3:158694184 | G | C | 1 | a0001c0001t0032 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2717G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2717 | chr3 | 158694184 | ||||||
| chr3:158694250 | TA | T | 5 | a0001c0001t0003 a0001c0001t0032 a0001c0001t0034 others(2): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2790delA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2790 | INFO_REALIGN_3_PRIME | chr3 | 158694250 | |||||
| chr3:158694376 | A | G | 1 | a0001c0001t0034 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2909A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2909 | chr3 | 158694376 | ||||||
| chr3:158694594 | C | T | 2 | a0001c0004t0025 a0001c0004t0026 |
2 | HG01243.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3127C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3127 | chr3 | 158694594 | ||||||
| chr3:158694660 | G | A | 1 | a0001c0001t0022 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3193G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3193 | chr3 | 158694660 | ||||||
| chr3:158694797 | T | G | 1 | a0001c0001t0014 | 3 | HG03098.hp2 HG03486.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3330T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3330 | chr3 | 158694797 | ||||||
| chr3:158694852 | GTAT | G | 1 | a0001c0001t0005 | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3390_*3392delATT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3390 | INFO_REALIGN_3_PRIME | chr3 | 158694852 | |||||
| chr3:158694857 | A | C | 1 | a0001c0001t0031 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3390A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3390 | chr3 | 158694857 | ||||||
| chr3:158695132 | G | C | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3665G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3665 | chr3 | 158695132 | ||||||
| chr3:158695134 | G | A | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3667G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3667 | chr3 | 158695134 | ||||||
| chr3:158695135 | A | G | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3668A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3668 | chr3 | 158695135 | ||||||
| chr3:158695136 | G | T | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3669G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3669 | chr3 | 158695136 | ||||||
| chr3:158695143 | G | C | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3676G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3676 | chr3 | 158695143 | ||||||
| chr3:158695153 | A | C | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(35): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*3686A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3686 | chr3 | 158695153 | ||||||
| chr3:158695230 | C | A | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3763C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3763 | chr3 | 158695230 | ||||||
| chr3:158695230 | C | T | 2 | a0001c0001t0011 a0009c0006t0011 |
4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3763C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3763 | chr3 | 158695230 | ||||||
| chr3:158695525 | C | A | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4058C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 4058 | chr3 | 158695525 | ||||||
| chr3:158695532 | A | C | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4065A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 4065 | chr3 | 158695532 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:158644737 | A | G | 142 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(139): Show |
160 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.81+22A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158644737 | |||||||
| chr3:158644779 | A | G | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.81+64A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158644779 | |||||||
| chr3:158644799 | C | G | 142 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(139): Show |
160 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.81+84C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158644799 | |||||||
| chr3:158644874 | A | G | 1 | a0001c0004t0026g0305 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+159A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158644874 | |||||||
| chr3:158644980 | GT | G | 63 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(60): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.81+283delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 158644980 | ||||||
| chr3:158644980 | GTT | G | 132 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(129): Show |
150 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.81+282_81+283delTT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 158644980 | ||||||
| chr3:158645260 | G | C | 1 | a0002c0002t0001g0083 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.82-369G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158645260 | |||||||
| chr3:158645266 | A | C | 142 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(139): Show |
160 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.82-363A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158645266 | |||||||
| chr3:158645431 | G | A | 2 | a0001c0001t0014g0178 a0001c0001t0014g0179 |
2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.82-198G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158645431 | |||||||
| chr3:158645511 | A | G | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.82-118A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158645511 | |||||||
| chr3:158645579 | G | T | 1 | a0001c0001t0014g0179 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.82-50G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158645579 | |||||||
| chr3:158645800 | T | A | 1 | a0001c0001t0004g0180 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.234+19T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 2/17 | chr3 | 158645800 | |||||||
| chr3:158645968 | A | G | 12 | a0001c0001t0009g0289 a0001c0001t0009g0290 a0001c0001t0009g0291 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.234+187A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 2/17 | chr3 | 158645968 | |||||||
| chr3:158646080 | G | C | 2 | a0002c0002t0001g0084 a0002c0002t0001g0085 |
2 | HG02056.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.235-85G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 2/17 | chr3 | 158646080 | |||||||
| chr3:158646520 | C | T | 60 | a0002c0002t0001g0007 a0002c0002t0001g0008 a0002c0002t0001g0011 others(57): Show |
73 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.367+223C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 3/17 | chr3 | 158646520 | |||||||
| chr3:158646544 | G | A | 59 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(56): Show |
65 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.368-199G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 3/17 | chr3 | 158646544 | |||||||
| chr3:158646566 | G | A | 2 | a0001c0001t0017g0028 a0001c0001t0030g0224 |
3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.368-177G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 3/17 | chr3 | 158646566 | |||||||
| chr3:158646709 | T | A | 2 | a0002c0002t0001g0086 a0002c0002t0001g0087 |
2 | HG02027.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.368-34T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 3/17 | chr3 | 158646709 | |||||||
| chr3:158646725 | A | G | 4 | a0001c0001t0005g0284 a0001c0001t0005g0285 a0001c0001t0005g0286 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-18A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 3/17 | chr3 | 158646725 | |||||||
| chr3:158647060 | T | C | 1 | a0002c0002t0001g0133 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.572+113T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647060 | |||||||
| chr3:158647338 | G | A | 2 | a0001c0001t0004g0225 a0001c0001t0004g0226 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.572+391G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647338 | |||||||
| chr3:158647406 | A | G | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.572+459A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647406 | |||||||
| chr3:158647444 | A | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.572+497A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647444 | |||||||
| chr3:158647460 | C | T | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.572+513C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647460 | |||||||
| chr3:158647461 | A | G | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.572+514A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647461 | |||||||
| chr3:158647489 | A | G | 8 | a0001c0001t0009g0289 a0001c0001t0009g0290 a0001c0001t0009g0291 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.572+542A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647489 | |||||||
| chr3:158647513 | C | G | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.572+566C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647513 | |||||||
| chr3:158647553 | C | T | 1 | a0001c0001t0015g0016 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.572+606C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647553 | |||||||
| chr3:158647660 | T | C | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.572+713T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647660 | |||||||
| chr3:158647667 | T | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.572+720T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647667 | |||||||
| chr3:158647679 | CATTTTCT others(4): Show |
C | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+733_572+743del others(11): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647679 | |||||||
| chr3:158647692 | G | T | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+745G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647692 | |||||||
| chr3:158647702 | A | T | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+755A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647702 | |||||||
| chr3:158647712 | T | G | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+765T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647712 | |||||||
| chr3:158647726 | T | A | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+779T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647726 | |||||||
| chr3:158647727 | A | G | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+780A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647727 | |||||||
| chr3:158647731 | T | A | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+784T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647731 | |||||||
| chr3:158647734 | A | G | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+787A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647734 | |||||||
| chr3:158647740 | A | T | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+793A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647740 | |||||||
| chr3:158647749 | A | G | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.572+802A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647749 | |||||||
| chr3:158647759 | A | T | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+812A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647759 | |||||||
| chr3:158647761 | A | C | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+814A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647761 | |||||||
| chr3:158647890 | A | G | 1 | a0001c0001t0004g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.572+943A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647890 | |||||||
| chr3:158647930 | C | T | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.572+983C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647930 | |||||||
| chr3:158648406 | C | T | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.573-635C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648406 | |||||||
| chr3:158648411 | G | T | 4 | a0001c0001t0002g0079 a0001c0001t0002g0080 a0001c0001t0002g0081 others(1): Show |
4 | HG02486.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.573-630G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648411 | |||||||
| chr3:158648416 | C | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.573-625C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648416 | |||||||
| chr3:158648417 | A | G | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.573-624A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648417 | |||||||
| chr3:158648495 | A | C | 4 | a0002c0002t0001g0010 a0002c0002t0001g0018 a0002c0002t0001g0132 others(1): Show |
6 | HG00140.hp2 HG00639.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.573-546A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648495 | |||||||
| chr3:158648539 | G | T | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.573-502G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648539 | |||||||
| chr3:158648571 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | HG01123.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.573-470G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648571 | |||||||
| chr3:158648625 | C | T | 58 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(55): Show |
69 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.573-416C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648625 | |||||||
| chr3:158648678 | C | CA | 8 | a0002c0002t0001g0091 a0002c0002t0001g0092 a0002c0002t0001g0093 others(5): Show |
8 | HG01074.hp2 HG01346.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.573-340dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 158648678 | ||||||
| chr3:158648678 | CA | C | 10 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(7): Show |
10 | HG00099.hp1 HG01168.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.573-340delA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 158648678 | ||||||
| chr3:158648678 | CAA | C | 55 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0029 others(52): Show |
64 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.573-341_573-340del others(2): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 158648678 | ||||||
| chr3:158648678 | CAAA | C | 134 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(131): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.573-342_573-340del others(3): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 158648678 | ||||||
| chr3:158648678 | CAAAA | C | 12 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0001c0001t0002g0078 others(9): Show |
12 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.573-343_573-340del others(4): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 158648678 | ||||||
| chr3:158649332 | T | TGAGAGAC others(26): Show |
1 | a0001c0001t0003g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.689+175_689+176ins others(33): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158649332 | |||||||
| chr3:158649357 | A | G | 4 | a0001c0001t0011g0227 a0001c0001t0011g0228 a0001c0001t0011g0229 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.689+200A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158649357 | |||||||
| chr3:158649637 | A | G | 1 | a0001c0001t0004g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.689+480A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158649637 | |||||||
| chr3:158649730 | T | C | 2 | a0001c0001t0015g0016 a0001c0001t0022g0033 |
3 | HG03490.hp1 HG03492.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.689+573T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158649730 | |||||||
| chr3:158649768 | A | G | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.689+611A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158649768 | |||||||
| chr3:158649809 | G | T | 2 | a0001c0001t0003g0218 a0001c0001t0003g0219 |
2 | NA18965.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.689+652G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158649809 | |||||||
| chr3:158650048 | C | T | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.689+891C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650048 | |||||||
| chr3:158650250 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.689+1093T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650250 | |||||||
| chr3:158650368 | A | C | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.689+1211A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650368 | |||||||
| chr3:158650428 | G | T | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.689+1271G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650428 | |||||||
| chr3:158650711 | T | G | 6 | a0001c0001t0003g0026 a0001c0001t0003g0183 a0001c0001t0003g0184 others(3): Show |
7 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-1385T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650711 | |||||||
| chr3:158650735 | A | C | 233 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(230): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.690-1361A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650735 | |||||||
| chr3:158650783 | A | G | 12 | a0002c0002t0001g0008 a0002c0002t0001g0020 a0002c0002t0001g0021 others(9): Show |
17 | HG00558.hp1 HG00597.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.690-1313A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650783 | |||||||
| chr3:158650808 | G | T | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.690-1288G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650808 | |||||||
| chr3:158650838 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.690-1258C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650838 | |||||||
| chr3:158650995 | T | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.690-1101T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650995 | |||||||
| chr3:158651012 | C | G | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.690-1084C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651012 | |||||||
| chr3:158651020 | C | CA | 81 | a0001c0001t0002g0034 a0001c0001t0002g0039 a0001c0001t0002g0040 others(78): Show |
85 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.690-1051dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 158651020 | ||||||
| chr3:158651020 | C | CAA | 20 | a0001c0001t0002g0035 a0001c0001t0003g0186 a0001c0001t0003g0218 others(17): Show |
20 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.690-1052_690-1051d others(4): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 158651020 | ||||||
| chr3:158651020 | C | CAAA | 47 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(44): Show |
58 | HG00323.hp1 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.690-1053_690-1051d others(5): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 158651020 | ||||||
| chr3:158651020 | C | CAAAA | 7 | a0001c0001t0004g0231 a0001c0001t0004g0232 a0001c0001t0004g0233 others(4): Show |
7 | HG00597.hp2 HG01175.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-1054_690-1051d others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 158651020 | ||||||
| chr3:158651020 | CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0003g0012 a0001c0001t0003g0027 a0001c0001t0003g0215 others(2): Show |
8 | HG02056.hp2 HG02129.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.690-1060_690-1051d others(12): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 158651020 | ||||||
| chr3:158651142 | C | T | 3 | a0001c0004t0024g0283 a0001c0004t0025g0300 a0001c0004t0026g0305 |
3 | HG01243.hp1 HG02647.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.690-954C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651142 | |||||||
| chr3:158651161 | C | G | 2 | a0001c0001t0003g0213 a0001c0001t0003g0214 |
2 | NA18954.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.690-935C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651161 | |||||||
| chr3:158651178 | A | G | 4 | a0001c0001t0011g0227 a0001c0001t0011g0228 a0001c0001t0011g0229 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-918A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651178 | |||||||
| chr3:158651212 | C | G | 1 | a0003c0003t0007g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.690-884C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651212 | |||||||
| chr3:158651284 | G | A | 1 | a0001c0001t0002g0043 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.690-812G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651284 | |||||||
| chr3:158651313 | T | G | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.690-783T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651313 | |||||||
| chr3:158651371 | T | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.690-725T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651371 | |||||||
| chr3:158651374 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.690-722G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651374 | |||||||
| chr3:158651640 | A | T | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.690-456A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651640 | |||||||
| chr3:158651663 | T | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.690-433T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651663 | |||||||
| chr3:158651781 | A | C | 1 | a0001c0001t0002g0074 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.690-315A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651781 | |||||||
| chr3:158651824 | AT | A | 142 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(139): Show |
160 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.690-262delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 158651824 | ||||||
| chr3:158652000 | T | A | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.690-96T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158652000 | |||||||
| chr3:158652009 | A | G | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.690-87A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158652009 | |||||||
| chr3:158652056 | G | A | 5 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(2): Show |
5 | NA18939.hp2 NA18962.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.690-40G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158652056 | |||||||
| chr3:158652335 | G | C | 1 | a0001c0001t0027g0236 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.840+89G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652335 | |||||||
| chr3:158652338 | T | C | 6 | a0001c0001t0009g0289 a0001c0001t0009g0290 a0001c0001t0009g0291 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+92T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652338 | |||||||
| chr3:158652354 | C | G | 2 | a0002c0002t0001g0019 a0002c0002t0001g0149 |
3 | HG03239.hp2 HG03704.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.840+108C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652354 | |||||||
| chr3:158652429 | T | C | 1 | a0001c0001t0003g0187 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.840+183T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652429 | |||||||
| chr3:158652563 | T | C | 2 | a0001c0001t0017g0028 a0001c0001t0030g0224 |
3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.840+317T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652563 | |||||||
| chr3:158652754 | A | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.840+508A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652754 | |||||||
| chr3:158652898 | C | T | 1 | a0001c0001t0005g0284 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.841-412C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652898 | |||||||
| chr3:158652945 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.841-365G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652945 | |||||||
| chr3:158652983 | C | T | 3 | a0001c0001t0014g0178 a0001c0001t0014g0179 a0001c0001t0014g0296 |
3 | HG03098.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.841-327C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652983 | |||||||
| chr3:158653014 | T | C | 1 | a0008c0011t0004g0299 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.841-296T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158653014 | |||||||
| chr3:158653086 | C | T | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.841-224C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158653086 | |||||||
| chr3:158653198 | C | T | 1 | a0002c0002t0001g0177 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.841-112C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158653198 | |||||||
| chr3:158653617 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.998+150G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158653617 | |||||||
| chr3:158653757 | T | TA | 136 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(133): Show |
154 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.998+302dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 158653757 | ||||||
| chr3:158653846 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.998+379G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158653846 | |||||||
| chr3:158653978 | G | C | 1 | a0001c0001t0004g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.998+511G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158653978 | |||||||
| chr3:158654066 | A | T | 1 | a0001c0001t0004g0265 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.999-481A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158654066 | |||||||
| chr3:158654204 | C | T | 1 | a0002c0002t0001g0125 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.999-343C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158654204 | |||||||
| chr3:158654205 | C | CT | 93 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.999-318dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 158654205 | ||||||
| chr3:158654205 | C | CTT | 78 | a0001c0001t0002g0032 a0001c0001t0002g0042 a0001c0001t0002g0046 others(75): Show |
88 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.999-319_999-318dup others(2): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 158654205 | ||||||
| chr3:158654205 | C | CTTT | 24 | a0001c0001t0003g0212 a0001c0001t0004g0013 a0001c0001t0004g0030 others(21): Show |
26 | HG00642.hp2 HG00735.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.999-320_999-318dup others(3): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 158654205 | ||||||
| chr3:158654205 | C | CTTTT | 6 | a0001c0001t0005g0281 a0001c0001t0005g0284 a0001c0001t0011g0228 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-321_999-318dup others(4): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 158654205 | ||||||
| chr3:158654300 | A | G | 4 | a0001c0001t0014g0178 a0001c0001t0014g0179 a0001c0001t0014g0296 others(1): Show |
4 | HG03098.hp2 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-247A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158654300 | |||||||
| chr3:158654326 | A | T | 4 | a0001c0001t0011g0227 a0001c0001t0011g0228 a0001c0001t0011g0229 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-221A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158654326 | |||||||
| chr3:158654436 | A | G | 1 | a0001c0001t0004g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.999-111A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158654436 | |||||||
| chr3:158654454 | T | A | 1 | a0001c0001t0003g0297 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.999-93T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158654454 | |||||||
| chr3:158654637 | T | G | 1 | a0001c0001t0003g0220 | 1 | HG00280.hp2 | splice_region_variant&intron_variant | LOW | c.1083+6T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158654637 | |||||||
| chr3:158654688 | C | T | 119 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(116): Show |
136 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1083+57C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158654688 | |||||||
| chr3:158654713 | T | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1083+82T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158654713 | |||||||
| chr3:158654886 | G | T | 2 | a0001c0001t0004g0233 a0001c0001t0004g0257 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1083+255G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158654886 | |||||||
| chr3:158655141 | A | G | 142 | a0001c0001t0002g0045 a0001c0001t0003g0009 a0001c0001t0003g0012 others(139): Show |
160 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1083+510A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655141 | |||||||
| chr3:158655156 | T | C | 1 | a0001c0001t0009g0289 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1083+525T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655156 | |||||||
| chr3:158655168 | A | G | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1083+537A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655168 | |||||||
| chr3:158655207 | T | A | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1083+576T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655207 | |||||||
| chr3:158655249 | G | A | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1083+618G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655249 | |||||||
| chr3:158655260 | C | T | 4 | a0001c0004t0024g0283 a0002c0002t0001g0086 a0002c0002t0001g0087 others(1): Show |
4 | HG02027.hp1 HG03017.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+629C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655260 | |||||||
| chr3:158655275 | G | T | 2 | a0002c0002t0001g0097 a0010c0014t0001g0094 |
2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1083+644G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655275 | |||||||
| chr3:158655300 | A | G | 1 | a0001c0001t0004g0256 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1083+669A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655300 | |||||||
| chr3:158655310 | C | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0215 |
3 | HG02129.hp1 HG03831.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1083+679C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655310 | |||||||
| chr3:158655408 | T | C | 143 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(140): Show |
161 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1083+777T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655408 | |||||||
| chr3:158655466 | A | T | 1 | a0001c0001t0002g0041 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1083+835A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655466 | |||||||
| chr3:158655485 | G | GA | 142 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(139): Show |
160 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1083+867dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158655485 | ||||||
| chr3:158655670 | T | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1083+1039T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655670 | |||||||
| chr3:158655761 | T | C | 60 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(57): Show |
71 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1083+1130T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655761 | |||||||
| chr3:158655872 | C | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1083+1241C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655872 | |||||||
| chr3:158655946 | C | T | 1 | a0001c0001t0003g0211 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1083+1315C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655946 | |||||||
| chr3:158656040 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1083+1409G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656040 | |||||||
| chr3:158656141 | GT | G | 200 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(197): Show |
231 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1083+1519delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158656141 | ||||||
| chr3:158656227 | C | T | 1 | a0002c0002t0001g0119 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1083+1596C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656227 | |||||||
| chr3:158656228 | G | A | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1083+1597G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656228 | |||||||
| chr3:158656230 | T | A | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1083+1599T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656230 | |||||||
| chr3:158656342 | A | G | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1083+1711A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656342 | |||||||
| chr3:158656372 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1083+1741C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656372 | |||||||
| chr3:158656427 | A | G | 1 | a0002c0002t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1083+1796A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656427 | |||||||
| chr3:158656433 | A | G | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1083+1802A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656433 | |||||||
| chr3:158656602 | T | TAAG | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1083+1971_1083+197 others(7): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656602 | |||||||
| chr3:158656700 | A | G | 2 | a0001c0001t0017g0028 a0001c0001t0030g0224 |
3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1083+2069A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656700 | |||||||
| chr3:158656737 | G | A | 1 | a0001c0001t0004g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1083+2106G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656737 | |||||||
| chr3:158656746 | C | G | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1083+2115C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656746 | |||||||
| chr3:158656911 | C | T | 4 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0173 others(1): Show |
4 | HG01081.hp2 NA18956.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-2011C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656911 | |||||||
| chr3:158656917 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1084-2005G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656917 | |||||||
| chr3:158656920 | T | C | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1084-2002T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656920 | |||||||
| chr3:158657035 | G | A | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1084-1887G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657035 | |||||||
| chr3:158657077 | A | C | 1 | a0001c0001t0003g0186 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1084-1845A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657077 | |||||||
| chr3:158657209 | A | T | 4 | a0001c0001t0014g0178 a0001c0001t0014g0179 a0001c0001t0014g0296 others(1): Show |
4 | HG03098.hp2 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084-1713A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657209 | |||||||
| chr3:158657251 | A | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1084-1671A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657251 | |||||||
| chr3:158657288 | A | T | 1 | a0001c0001t0003g0210 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1084-1634A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657288 | |||||||
| chr3:158657290 | AT | A | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1084-1628delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158657290 | ||||||
| chr3:158657634 | G | A | 2 | a0001c0001t0004g0225 a0001c0001t0004g0226 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1084-1288G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657634 | |||||||
| chr3:158657654 | T | G | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1084-1268T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657654 | |||||||
| chr3:158657840 | T | C | 1 | a0002c0002t0001g0100 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1084-1082T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657840 | |||||||
| chr3:158657869 | T | C | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1084-1053T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657869 | |||||||
| chr3:158657999 | C | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1084-923C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657999 | |||||||
| chr3:158658054 | G | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1084-868G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158658054 | |||||||
| chr3:158658157 | C | CT | 6 | a0002c0002t0001g0083 a0002c0002t0001g0096 a0002c0002t0001g0098 others(3): Show |
6 | HG01978.hp2 HG02055.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084-742dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | ||||||
| chr3:158658157 | C | CTTT | 46 | a0001c0001t0004g0029 a0001c0001t0004g0233 a0001c0001t0004g0245 others(43): Show |
47 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.1084-744_1084-742d others(5): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | ||||||
| chr3:158658157 | C | CTTTT | 17 | a0001c0001t0003g0190 a0001c0001t0003g0213 a0001c0001t0003g0223 others(14): Show |
18 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1084-745_1084-742d others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | ||||||
| chr3:158658157 | C | CTTTTT | 28 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0027 others(25): Show |
33 | HG00280.hp2 HG00609.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1084-746_1084-742d others(7): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | ||||||
| chr3:158658157 | C | CTTTTTT | 18 | a0001c0001t0003g0026 a0001c0001t0003g0183 a0001c0001t0003g0184 others(15): Show |
19 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1084-747_1084-742d others(8): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | ||||||
| chr3:158658157 | CT | C | 11 | a0001c0001t0002g0040 a0001c0001t0002g0047 a0001c0001t0002g0079 others(8): Show |
11 | HG01081.hp2 HG01168.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084-742delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | ||||||
| chr3:158658157 | CTT | C | 52 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(49): Show |
65 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.1084-743_1084-742d others(4): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | ||||||
| chr3:158658157 | CTTTT | C | 28 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(25): Show |
38 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1084-745_1084-742d others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | ||||||
| chr3:158658215 | G | A | 3 | a0002c0002t0001g0086 a0002c0002t0001g0087 a0002c0002t0001g0124 |
3 | HG02027.hp1 HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1084-707G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158658215 | |||||||
| chr3:158658367 | G | C | 60 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(57): Show |
71 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1084-555G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158658367 | |||||||
| chr3:158658411 | C | T | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1084-511C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158658411 | |||||||
| chr3:158658565 | C | G | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1084-357C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158658565 | |||||||
| chr3:158658866 | T | A | 1 | a0001c0001t0002g0042 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1084-56T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158658866 | |||||||
| chr3:158659162 | A | G | 1 | a0001c0001t0013g0275 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1221+103A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659162 | |||||||
| chr3:158659262 | G | A | 2 | a0001c0001t0018g0294 a0001c0001t0018g0304 |
2 | HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1221+203G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659262 | |||||||
| chr3:158659281 | T | C | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1221+222T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659281 | |||||||
| chr3:158659352 | C | A | 1 | a0001c0001t0004g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1221+293C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659352 | |||||||
| chr3:158659382 | T | C | 1 | a0001c0009t0029g0295 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1221+323T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659382 | |||||||
| chr3:158659513 | T | C | 1 | a0002c0002t0001g0138 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1221+454T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659513 | |||||||
| chr3:158659653 | C | G | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1221+594C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659653 | |||||||
| chr3:158659681 | G | A | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1221+622G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659681 | |||||||
| chr3:158659695 | T | G | 4 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0173 others(1): Show |
4 | HG01081.hp2 NA18956.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221+636T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659695 | |||||||
| chr3:158659702 | A | G | 126 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(123): Show |
143 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1221+643A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659702 | |||||||
| chr3:158659765 | G | T | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1221+706G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659765 | |||||||
| chr3:158659780 | C | T | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1221+721C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659780 | |||||||
| chr3:158659877 | G | T | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1221+818G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659877 | |||||||
| chr3:158660008 | C | G | 201 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(198): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1222-866C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660008 | |||||||
| chr3:158660124 | C | T | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1222-750C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660124 | |||||||
| chr3:158660248 | C | CT | 79 | a0001c0001t0002g0032 a0001c0001t0003g0009 a0001c0001t0003g0012 others(76): Show |
86 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.1222-611dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 158660248 | ||||||
| chr3:158660367 | C | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1222-507C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660367 | |||||||
| chr3:158660420 | G | C | 5 | a0001c0001t0002g0040 a0001c0001t0002g0051 a0001c0001t0002g0075 others(2): Show |
5 | NA18949.hp1 NA18968.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222-454G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660420 | |||||||
| chr3:158660463 | G | A | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1222-411G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660463 | |||||||
| chr3:158660494 | C | T | 56 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(53): Show |
69 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1222-380C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660494 | |||||||
| chr3:158660495 | G | A | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1222-379G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660495 | |||||||
| chr3:158660539 | T | C | 1 | a0001c0001t0003g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1222-335T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660539 | |||||||
| chr3:158660544 | C | T | 1 | a0001c0001t0004g0260 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1222-330C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660544 | |||||||
| chr3:158660553 | A | G | 2 | a0001c0001t0017g0028 a0001c0001t0030g0224 |
3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1222-321A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660553 | |||||||
| chr3:158660615 | G | C | 4 | a0001c0001t0014g0178 a0001c0001t0014g0179 a0001c0001t0014g0296 others(1): Show |
4 | HG03098.hp2 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222-259G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660615 | |||||||
| chr3:158660738 | C | G | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1222-136C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660738 | |||||||
| chr3:158660871 | T | G | 1 | a0002c0002t0001g0158 | 1 | HG02300.hp1 | splice_region_variant&intron_variant | LOW | c.1222-3T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660871 | |||||||
| chr3:158661047 | A | G | 28 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(25): Show |
38 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1323+72A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661047 | |||||||
| chr3:158661058 | A | G | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1323+83A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661058 | |||||||
| chr3:158661299 | T | A | 1 | a0002c0002t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1323+324T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661299 | |||||||
| chr3:158661383 | G | C | 27 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(24): Show |
37 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1323+408G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661383 | |||||||
| chr3:158661439 | A | G | 4 | a0001c0001t0002g0079 a0001c0001t0002g0080 a0001c0001t0002g0081 others(1): Show |
4 | HG02486.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1323+464A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661439 | |||||||
| chr3:158661612 | C | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1323+637C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661612 | |||||||
| chr3:158661707 | A | G | 1 | a0002c0002t0001g0116 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1323+732A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661707 | |||||||
| chr3:158661742 | T | C | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1323+767T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661742 | |||||||
| chr3:158661764 | A | G | 2 | a0001c0001t0004g0225 a0001c0001t0004g0226 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1323+789A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661764 | |||||||
| chr3:158661860 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1324-768G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661860 | |||||||
| chr3:158661874 | G | A | 1 | a0002c0002t0001g0133 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1324-754G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661874 | |||||||
| chr3:158662156 | G | A | 3 | a0002c0002t0001g0120 a0002c0002t0001g0128 a0002c0013t0001g0101 |
3 | NA18947.hp1 NA18957.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1324-472G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158662156 | |||||||
| chr3:158662164 | G | C | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1324-464G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158662164 | |||||||
| chr3:158662361 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1324-267G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158662361 | |||||||
| chr3:158662438 | T | C | 1 | a0002c0002t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1324-190T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158662438 | |||||||
| chr3:158662833 | T | C | 1 | a0002c0002t0001g0152 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1380+149T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158662833 | |||||||
| chr3:158662905 | T | A | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1380+221T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158662905 | |||||||
| chr3:158662996 | C | A | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1380+312C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158662996 | |||||||
| chr3:158663288 | A | G | 1 | a0001c0001t0002g0075 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1380+604A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158663288 | |||||||
| chr3:158663301 | A | C | 1 | a0002c0002t0001g0177 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1380+617A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158663301 | |||||||
| chr3:158663458 | A | G | 1 | a0002c0002t0001g0149 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1380+774A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158663458 | |||||||
| chr3:158663511 | TC | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1380+829delC | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 158663511 | ||||||
| chr3:158663598 | G | C | 3 | a0001c0001t0014g0178 a0001c0001t0014g0179 a0001c0001t0014g0296 |
3 | HG03098.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1380+914G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158663598 | |||||||
| chr3:158663789 | A | G | 4 | a0001c0001t0011g0227 a0001c0001t0011g0228 a0001c0001t0011g0229 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1380+1105A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158663789 | |||||||
| chr3:158664045 | A | G | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1381-1292A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664045 | |||||||
| chr3:158664304 | G | A | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1381-1033G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664304 | |||||||
| chr3:158664440 | T | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1381-897T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664440 | |||||||
| chr3:158664523 | C | A | 2 | a0001c0001t0017g0028 a0001c0001t0030g0224 |
3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1381-814C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664523 | |||||||
| chr3:158664603 | A | T | 1 | a0001c0001t0003g0188 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1381-734A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664603 | |||||||
| chr3:158664733 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1381-604G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664733 | |||||||
| chr3:158664760 | T | C | 1 | a0001c0009t0029g0295 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1381-577T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664760 | |||||||
| chr3:158664831 | A | G | 58 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(55): Show |
69 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1381-506A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664831 | |||||||
| chr3:158664929 | A | G | 7 | a0001c0001t0004g0029 a0001c0001t0004g0233 a0001c0001t0004g0244 others(4): Show |
8 | HG02257.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1381-408A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664929 | |||||||
| chr3:158665054 | G | T | 1 | a0001c0001t0002g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1381-283G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158665054 | |||||||
| chr3:158665060 | A | G | 3 | a0001c0004t0024g0283 a0001c0004t0025g0300 a0001c0004t0026g0305 |
3 | HG01243.hp1 HG02647.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1381-277A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158665060 | |||||||
| chr3:158665100 | G | A | 1 | a0001c0001t0009g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1381-237G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158665100 | |||||||
| chr3:158665298 | C | T | 1 | a0003c0003t0007g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1381-39C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158665298 | |||||||
| chr3:158665734 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1518+260A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158665734 | |||||||
| chr3:158665915 | T | C | 58 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(55): Show |
69 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1519-389T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158665915 | |||||||
| chr3:158665935 | A | G | 1 | a0002c0002t0001g0115 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1519-369A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158665935 | |||||||
| chr3:158666093 | T | C | 139 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(136): Show |
157 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1519-211T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158666093 | |||||||
| chr3:158666093 | T | G | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1519-211T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158666093 | |||||||
| chr3:158666271 | A | T | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1519-33A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158666271 | |||||||
| chr3:158666279 | A | G | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1519-25A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158666279 | |||||||
| chr3:158666395 | G | C | 4 | a0001c0001t0011g0227 a0001c0001t0011g0228 a0001c0001t0011g0229 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1601+9G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158666395 | |||||||
| chr3:158666424 | A | G | 7 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0039 others(4): Show |
11 | HG02074.hp1 NA18747.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.1601+38A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158666424 | |||||||
| chr3:158666476 | T | G | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1601+90T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158666476 | |||||||
| chr3:158666573 | A | G | 1 | a0002c0002t0019g0114 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1601+187A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158666573 | |||||||
| chr3:158666674 | C | T | 2 | a0001c0001t0004g0243 a0001c0001t0004g0274 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1601+288C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158666674 | |||||||
| chr3:158666944 | C | A | 60 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(57): Show |
71 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1601+558C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158666944 | |||||||
| chr3:158667094 | C | A | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1601+708C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158667094 | |||||||
| chr3:158667097 | G | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1601+711G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158667097 | |||||||
| chr3:158667131 | C | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+745C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158667131 | |||||||
| chr3:158667617 | C | A | 1 | a0001c0001t0002g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1601+1231C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158667617 | |||||||
| chr3:158667757 | C | T | 1 | a0001c0009t0029g0295 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1601+1371C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158667757 | |||||||
| chr3:158667926 | T | C | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1601+1540T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158667926 | |||||||
| chr3:158668007 | G | C | 26 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(23): Show |
36 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1601+1621G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668007 | |||||||
| chr3:158668086 | A | G | 1 | a0002c0002t0001g0127 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1601+1700A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668086 | |||||||
| chr3:158668136 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0072 |
2 | HG00558.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1601+1750C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668136 | |||||||
| chr3:158668177 | G | C | 239 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(236): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1601+1791G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668177 | |||||||
| chr3:158668249 | C | A | 1 | a0001c0001t0003g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1601+1863C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668249 | |||||||
| chr3:158668345 | A | G | 1 | a0002c0002t0001g0110 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1601+1959A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668345 | |||||||
| chr3:158668438 | T | C | 2 | a0001c0001t0003g0192 a0001c0001t0003g0223 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1601+2052T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668438 | |||||||
| chr3:158668718 | A | G | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+2332A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668718 | |||||||
| chr3:158668750 | G | A | 3 | a0001c0001t0002g0079 a0001c0001t0002g0081 a0011c0010t0002g0090 |
3 | HG02965.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1601+2364G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668750 | |||||||
| chr3:158668800 | A | G | 9 | a0002c0002t0001g0004 a0002c0002t0001g0092 a0002c0002t0001g0096 others(6): Show |
13 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1601+2414A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668800 | |||||||
| chr3:158668908 | A | G | 15 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(12): Show |
16 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1601+2522A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668908 | |||||||
| chr3:158668944 | C | T | 1 | a0001c0001t0004g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1601+2558C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668944 | |||||||
| chr3:158668948 | C | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+2562C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668948 | |||||||
| chr3:158669002 | C | T | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1601+2616C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158669002 | |||||||
| chr3:158669097 | C | T | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1601+2711C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158669097 | |||||||
| chr3:158669102 | G | A | 15 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(12): Show |
16 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1601+2716G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158669102 | |||||||
| chr3:158669698 | T | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+3312T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158669698 | |||||||
| chr3:158670050 | T | G | 1 | a0001c0001t0004g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1601+3664T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670050 | |||||||
| chr3:158670308 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1601+3922C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670308 | |||||||
| chr3:158670372 | C | T | 1 | a0001c0001t0003g0189 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1601+3986C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670372 | |||||||
| chr3:158670439 | GC | G | 15 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(12): Show |
16 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1601+4056delC | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158670439 | ||||||
| chr3:158670605 | T | G | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+4219T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670605 | |||||||
| chr3:158670837 | G | A | 1 | a0002c0002t0001g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1601+4451G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670837 | |||||||
| chr3:158670917 | A | G | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1601+4531A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670917 | |||||||
| chr3:158670932 | C | CAAAGAAA | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+4554_1601+456 others(11): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158670932 | ||||||
| chr3:158670991 | T | C | 201 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(198): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1601+4605T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670991 | |||||||
| chr3:158671006 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1601+4620C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671006 | |||||||
| chr3:158671055 | A | G | 7 | a0001c0001t0003g0206 a0001c0001t0003g0210 a0001c0001t0003g0212 others(4): Show |
7 | HG00423.hp1 NA18954.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.1601+4669A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671055 | |||||||
| chr3:158671174 | A | C | 2 | a0001c0001t0004g0225 a0001c0001t0004g0226 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1601+4788A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671174 | |||||||
| chr3:158671339 | G | A | 60 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(57): Show |
71 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1601+4953G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671339 | |||||||
| chr3:158671601 | A | G | 1 | a0002c0002t0001g0085 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1601+5215A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671601 | |||||||
| chr3:158671601 | A | T | 1 | a0001c0001t0004g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1601+5215A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671601 | |||||||
| chr3:158671864 | C | G | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1601+5478C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671864 | |||||||
| chr3:158671983 | C | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+5597C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671983 | |||||||
| chr3:158672071 | C | T | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1601+5685C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672071 | |||||||
| chr3:158672084 | T | C | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1601+5698T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672084 | |||||||
| chr3:158672347 | C | T | 1 | a0002c0002t0001g0093 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1601+5961C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672347 | |||||||
| chr3:158672433 | C | T | 1 | a0001c0001t0004g0241 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1601+6047C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672433 | |||||||
| chr3:158672441 | G | A | 2 | a0001c0001t0016g0036 a0001c0001t0016g0048 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1601+6055G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672441 | |||||||
| chr3:158672445 | T | G | 1 | a0001c0001t0005g0277 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1601+6059T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672445 | |||||||
| chr3:158672606 | A | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+6220A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672606 | |||||||
| chr3:158672706 | C | T | 2 | a0001c0001t0003g0192 a0001c0001t0003g0223 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1601+6320C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672706 | |||||||
| chr3:158672745 | G | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0072 |
2 | HG00558.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1601+6359G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672745 | |||||||
| chr3:158672761 | A | T | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1601+6375A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672761 | |||||||
| chr3:158673037 | C | T | 1 | a0001c0001t0004g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1601+6651C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673037 | |||||||
| chr3:158673046 | C | G | 1 | a0001c0001t0005g0281 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1601+6660C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673046 | |||||||
| chr3:158673169 | T | C | 6 | a0001c0001t0004g0234 a0001c0001t0004g0245 a0001c0001t0004g0246 others(3): Show |
6 | HG01243.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1601+6783T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673169 | |||||||
| chr3:158673195 | A | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1601+6809A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673195 | |||||||
| chr3:158673306 | A | G | 5 | a0001c0001t0002g0040 a0001c0001t0002g0051 a0001c0001t0002g0075 others(2): Show |
5 | NA18949.hp1 NA18968.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1601+6920A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673306 | |||||||
| chr3:158673332 | A | C | 1 | a0002c0002t0001g0123 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1601+6946A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673332 | |||||||
| chr3:158673335 | C | G | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+6949C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673335 | |||||||
| chr3:158673349 | G | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+6963G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673349 | |||||||
| chr3:158673364 | A | G | 2 | a0002c0002t0001g0105 a0002c0002t0001g0129 |
2 | HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1601+6978A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673364 | |||||||
| chr3:158673508 | C | CT | 7 | a0001c0001t0023g0306 a0001c0004t0025g0300 a0001c0004t0026g0305 others(4): Show |
7 | HG01243.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1601+7142dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158673508 | ||||||
| chr3:158673508 | C | CTTT | 71 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(68): Show |
77 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1601+7140_1601+714 others(7): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158673508 | ||||||
| chr3:158673511 | T | TTC | 59 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(56): Show |
70 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.1601+7126_1601+712 others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158673511 | ||||||
| chr3:158673513 | T | C | 1 | a0002c0002t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1601+7127T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673513 | |||||||
| chr3:158673514 | T | C | 58 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(55): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.1601+7128T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673514 | |||||||
| chr3:158673515 | T | C | 1 | a0001c0001t0002g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1601+7129T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673515 | |||||||
| chr3:158673640 | T | C | 1 | a0001c0001t0005g0285 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1601+7254T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673640 | |||||||
| chr3:158673673 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+7287G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673673 | |||||||
| chr3:158673693 | A | G | 1 | a0001c0009t0029g0295 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1601+7307A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673693 | |||||||
| chr3:158673712 | T | G | 4 | a0001c0001t0002g0079 a0001c0001t0002g0080 a0001c0001t0002g0081 others(1): Show |
4 | HG02486.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601+7326T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673712 | |||||||
| chr3:158673725 | AAC | A | 2 | a0001c0001t0017g0028 a0001c0001t0030g0224 |
3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1601+7340_1601+734 others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673725 | |||||||
| chr3:158673781 | G | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+7395G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673781 | |||||||
| chr3:158673789 | C | A | 1 | a0001c0001t0004g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1601+7403C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673789 | |||||||
| chr3:158673830 | C | G | 1 | a0001c0001t0002g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1601+7444C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673830 | |||||||
| chr3:158673853 | A | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+7467A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673853 | |||||||
| chr3:158673924 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1601+7538A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673924 | |||||||
| chr3:158673956 | CT | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+7573delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158673956 | ||||||
| chr3:158674056 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+7670G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674056 | |||||||
| chr3:158674080 | C | CT | 9 | a0001c0001t0002g0076 a0001c0001t0002g0088 a0001c0001t0003g0205 others(6): Show |
9 | HG02145.hp1 HG02145.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1601+7711dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158674080 | ||||||
| chr3:158674080 | CT | C | 63 | a0001c0001t0002g0053 a0001c0001t0002g0062 a0001c0001t0003g0214 others(60): Show |
74 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.1601+7711delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158674080 | ||||||
| chr3:158674086 | T | C | 1 | a0002c0002t0001g0159 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1601+7700T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674086 | |||||||
| chr3:158674130 | C | G | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1601+7744C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674130 | |||||||
| chr3:158674167 | A | G | 309 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(306): Show |
367 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.1601+7781A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674167 | |||||||
| chr3:158674216 | G | C | 1 | a0003c0003t0007g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1602-7779G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674216 | |||||||
| chr3:158674425 | C | T | 2 | a0002c0002t0001g0017 a0002c0002t0001g0104 |
3 | HG02717.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1602-7570C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674425 | |||||||
| chr3:158674437 | C | T | 52 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(49): Show |
63 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1602-7558C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674437 | |||||||
| chr3:158674489 | T | C | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1602-7506T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674489 | |||||||
| chr3:158674684 | C | T | 7 | a0001c0001t0004g0029 a0001c0001t0004g0233 a0001c0001t0004g0244 others(4): Show |
8 | HG02257.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1602-7311C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674684 | |||||||
| chr3:158674699 | A | T | 7 | a0001c0001t0003g0187 a0001c0001t0003g0193 a0001c0001t0003g0199 others(4): Show |
7 | HG01074.hp1 HG01361.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602-7296A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674699 | |||||||
| chr3:158674710 | C | G | 1 | a0002c0002t0001g0123 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1602-7285C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674710 | |||||||
| chr3:158674730 | T | C | 1 | a0001c0001t0003g0189 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1602-7265T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674730 | |||||||
| chr3:158674738 | G | A | 1 | a0002c0002t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1602-7257G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674738 | |||||||
| chr3:158674931 | A | C | 2 | a0002c0002t0012g0082 a0002c0002t0012g0150 |
2 | NA18985.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1602-7064A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674931 | |||||||
| chr3:158675011 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-6984G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675011 | |||||||
| chr3:158675014 | A | T | 2 | a0001c0001t0004g0244 a0001c0001t0004g0253 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1602-6981A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675014 | |||||||
| chr3:158675025 | A | G | 1 | a0001c0001t0009g0293 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1602-6970A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675025 | |||||||
| chr3:158675147 | C | T | 2 | a0001c0001t0003g0191 a0001c0001t0003g0198 |
2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1602-6848C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675147 | |||||||
| chr3:158675154 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1602-6841G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675154 | |||||||
| chr3:158675156 | G | A | 1 | a0002c0002t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1602-6839G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675156 | |||||||
| chr3:158675157 | GGCGCCTG others(8): Show |
G | 5 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602-6835_1602-682 others(19): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158675157 | ||||||
| chr3:158675159 | C | T | 1 | a0001c0001t0005g0286 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1602-6836C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675159 | |||||||
| chr3:158675161 | C | T | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-6834C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675161 | |||||||
| chr3:158675218 | G | A | 3 | a0002c0002t0001g0097 a0002c0002t0001g0118 a0010c0014t0001g0094 |
3 | HG02109.hp2 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1602-6777G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675218 | |||||||
| chr3:158675285 | C | CA | 17 | a0002c0002t0001g0024 a0002c0002t0001g0085 a0002c0002t0001g0095 others(14): Show |
18 | HG00597.hp1 HG00621.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1602-6685dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158675285 | ||||||
| chr3:158675285 | CA | C | 66 | a0001c0001t0003g0183 a0001c0001t0003g0187 a0001c0001t0003g0194 others(63): Show |
77 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1602-6685delA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158675285 | ||||||
| chr3:158675285 | CAA | C | 47 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(44): Show |
53 | HG00280.hp2 HG01069.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.1602-6686_1602-668 others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158675285 | ||||||
| chr3:158675285 | CAAAAAAA others(5): Show |
C | 1 | a0002c0002t0001g0168 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1602-6696_1602-668 others(16): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158675285 | ||||||
| chr3:158675285 | CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602-6697_1602-668 others(17): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158675285 | ||||||
| chr3:158675305 | A | C | 3 | a0002c0002t0001g0083 a0002c0002t0001g0145 a0002c0002t0001g0146 |
3 | HG03491.hp2 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1602-6690A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675305 | |||||||
| chr3:158675306 | A | C | 2 | a0002c0002t0001g0128 a0002c0013t0001g0101 |
2 | NA18947.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1602-6689A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675306 | |||||||
| chr3:158675309 | A | AG | 22 | a0001c0001t0002g0035 a0001c0001t0002g0044 a0001c0001t0002g0047 others(19): Show |
22 | HG00423.hp2 HG01109.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1602-6686_1602-668 others(5): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675309 | |||||||
| chr3:158675309 | A | G | 179 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(176): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1602-6686A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675309 | |||||||
| chr3:158675310 | A | G | 201 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(198): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1602-6685A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675310 | |||||||
| chr3:158675389 | A | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-6606A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675389 | |||||||
| chr3:158675587 | A | G | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1602-6408A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675587 | |||||||
| chr3:158675631 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1602-6364G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675631 | |||||||
| chr3:158675899 | A | G | 2 | a0002c0002t0001g0096 a0002c0002t0001g0099 |
2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1602-6096A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675899 | |||||||
| chr3:158675933 | T | G | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-6062T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675933 | |||||||
| chr3:158675961 | T | C | 1 | a0001c0001t0002g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1602-6034T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675961 | |||||||
| chr3:158676059 | G | A | 1 | a0009c0006t0011g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1602-5936G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676059 | |||||||
| chr3:158676150 | T | G | 12 | a0001c0001t0009g0289 a0001c0001t0009g0290 a0001c0001t0009g0291 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1602-5845T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676150 | |||||||
| chr3:158676220 | T | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1602-5775T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676220 | |||||||
| chr3:158676224 | A | G | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1602-5771A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676224 | |||||||
| chr3:158676321 | T | G | 1 | a0001c0001t0004g0273 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1602-5674T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676321 | |||||||
| chr3:158676324 | G | A | 1 | a0001c0001t0004g0273 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1602-5671G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676324 | |||||||
| chr3:158676324 | G | GA | 140 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(137): Show |
158 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.1602-5668dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158676324 | ||||||
| chr3:158676431 | C | T | 1 | a0001c0001t0014g0296 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1602-5564C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676431 | |||||||
| chr3:158676701 | C | CT | 13 | a0001c0001t0003g0197 a0001c0001t0005g0277 a0001c0001t0005g0278 others(10): Show |
13 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1602-5279dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158676701 | ||||||
| chr3:158676701 | CT | C | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1602-5279delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158676701 | ||||||
| chr3:158676721 | CAG | C | 1 | a0001c0001t0003g0012 | 3 | NA18955.hp1 NA19056.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1602-5271_1602-527 others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158676721 | ||||||
| chr3:158676785 | C | T | 1 | a0002c0002t0001g0121 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1602-5210C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676785 | |||||||
| chr3:158676910 | G | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1602-5085G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676910 | |||||||
| chr3:158676947 | G | A | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1602-5048G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676947 | |||||||
| chr3:158676995 | C | T | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1602-5000C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676995 | |||||||
| chr3:158677008 | A | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1602-4987A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677008 | |||||||
| chr3:158677124 | T | C | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1602-4871T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677124 | |||||||
| chr3:158677155 | A | G | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1602-4840A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677155 | |||||||
| chr3:158677262 | A | C | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1602-4733A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677262 | |||||||
| chr3:158677304 | G | A | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-4691G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677304 | |||||||
| chr3:158677416 | A | G | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1602-4579A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677416 | |||||||
| chr3:158677540 | G | A | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-4455G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677540 | |||||||
| chr3:158677575 | A | G | 1 | a0001c0001t0004g0256 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1602-4420A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677575 | |||||||
| chr3:158677662 | G | A | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1602-4333G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677662 | |||||||
| chr3:158677669 | T | C | 2 | a0002c0002t0001g0141 a0002c0002t0001g0142 |
2 | NA18946.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1602-4326T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677669 | |||||||
| chr3:158677754 | G | A | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-4241G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677754 | |||||||
| chr3:158677881 | G | A | 199 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(196): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1602-4114G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677881 | |||||||
| chr3:158677888 | G | A | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1602-4107G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677888 | |||||||
| chr3:158677950 | G | C | 8 | a0001c0001t0007g0255 a0003c0003t0007g0230 a0003c0003t0007g0235 others(5): Show |
8 | HG01175.hp1 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1602-4045G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677950 | |||||||
| chr3:158678077 | G | C | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1602-3918G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678077 | |||||||
| chr3:158678101 | T | C | 1 | a0001c0001t0004g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1602-3894T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678101 | |||||||
| chr3:158678217 | A | C | 1 | a0001c0001t0003g0197 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1602-3778A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678217 | |||||||
| chr3:158678297 | T | C | 1 | a0001c0001t0005g0286 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1602-3698T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678297 | |||||||
| chr3:158678310 | G | A | 1 | a0002c0002t0001g0018 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1602-3685G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678310 | |||||||
| chr3:158678389 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1602-3606C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678389 | |||||||
| chr3:158678617 | A | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-3378A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678617 | |||||||
| chr3:158678696 | T | TAAA | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-3298_1602-329 others(7): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158678696 | ||||||
| chr3:158678735 | G | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-3260G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678735 | |||||||
| chr3:158678796 | C | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-3199C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678796 | |||||||
| chr3:158678856 | A | G | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-3139A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678856 | |||||||
| chr3:158679047 | A | T | 8 | a0001c0001t0007g0255 a0003c0003t0007g0230 a0003c0003t0007g0235 others(5): Show |
8 | HG01175.hp1 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1602-2948A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679047 | |||||||
| chr3:158679052 | C | T | 12 | a0001c0001t0009g0289 a0001c0001t0009g0290 a0001c0001t0009g0291 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1602-2943C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679052 | |||||||
| chr3:158679058 | C | T | 1 | a0001c0001t0004g0256 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1602-2937C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679058 | |||||||
| chr3:158679417 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-2578G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679417 | |||||||
| chr3:158679466 | T | TA | 3 | a0002c0002t0001g0138 a0002c0002t0001g0143 a0005c0015t0001g0140 |
3 | HG01109.hp1 HG01123.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1602-2528dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158679466 | ||||||
| chr3:158679514 | A | G | 1 | a0001c0001t0005g0280 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1602-2481A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679514 | |||||||
| chr3:158679535 | A | G | 2 | a0002c0002t0001g0136 a0002c0002t0001g0169 |
2 | NA19055.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1602-2460A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679535 | |||||||
| chr3:158679588 | C | T | 1 | a0001c0001t0004g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1602-2407C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679588 | |||||||
| chr3:158679910 | G | A | 3 | a0001c0004t0024g0283 a0001c0004t0025g0300 a0001c0004t0026g0305 |
3 | HG01243.hp1 HG02647.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1602-2085G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679910 | |||||||
| chr3:158680007 | C | T | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-1988C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680007 | |||||||
| chr3:158680053 | C | T | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1602-1942C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680053 | |||||||
| chr3:158680063 | G | C | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1602-1932G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680063 | |||||||
| chr3:158680164 | A | C | 1 | a0002c0002t0001g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1602-1831A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680164 | |||||||
| chr3:158680166 | A | T | 1 | a0002c0002t0001g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1602-1829A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680166 | |||||||
| chr3:158680195 | G | C | 1 | a0001c0001t0027g0236 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1602-1800G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680195 | |||||||
| chr3:158680221 | G | A | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1602-1774G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680221 | |||||||
| chr3:158680275 | AG | A | 9 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1602-1718delG | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158680275 | ||||||
| chr3:158680432 | G | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-1563G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680432 | |||||||
| chr3:158680491 | G | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-1504G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680491 | |||||||
| chr3:158680492 | G | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-1503G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680492 | |||||||
| chr3:158680531 | A | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-1464A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680531 | |||||||
| chr3:158680779 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1602-1216T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680779 | |||||||
| chr3:158680795 | C | G | 1 | a0001c0001t0003g0203 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1602-1200C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680795 | |||||||
| chr3:158680849 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-1146G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680849 | |||||||
| chr3:158680927 | C | T | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1602-1068C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680927 | |||||||
| chr3:158681482 | C | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1602-513C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158681482 | |||||||
| chr3:158681545 | TAATGCCC others(10): Show |
T | 2 | a0001c0004t0025g0300 a0001c0004t0026g0305 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-448_1602-432d others(19): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158681545 | ||||||
| chr3:158681798 | C | T | 3 | a0001c0001t0014g0178 a0001c0001t0014g0179 a0001c0001t0014g0296 |
3 | HG03098.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1602-197C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158681798 | |||||||
| chr3:158681968 | A | AT | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-17dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158681968 | ||||||
| chr3:158682472 | A | T | 7 | a0002c0002t0001g0008 a0002c0002t0001g0022 a0002c0002t0001g0023 others(4): Show |
11 | HG00597.hp1 HG02040.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1764+315A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158682472 | |||||||
| chr3:158682473 | T | C | 1 | a0001c0001t0003g0193 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1764+316T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158682473 | |||||||
| chr3:158682587 | T | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1764+430T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158682587 | |||||||
| chr3:158682710 | T | C | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1764+553T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158682710 | |||||||
| chr3:158682747 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1764+590G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158682747 | |||||||
| chr3:158682790 | C | T | 7 | a0001c0001t0004g0029 a0001c0001t0004g0233 a0001c0001t0004g0244 others(4): Show |
8 | HG02257.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1764+633C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158682790 | |||||||
| chr3:158683036 | G | GA | 37 | a0001c0001t0002g0032 a0001c0001t0002g0047 a0001c0001t0002g0054 others(34): Show |
39 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1764+896dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 158683036 | ||||||
| chr3:158683243 | A | G | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1764+1086A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683243 | |||||||
| chr3:158683320 | T | C | 1 | a0002c0002t0001g0126 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1764+1163T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683320 | |||||||
| chr3:158683327 | G | A | 3 | a0001c0001t0014g0178 a0001c0001t0014g0179 a0001c0001t0014g0296 |
3 | HG03098.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1764+1170G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683327 | |||||||
| chr3:158683377 | T | G | 28 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(25): Show |
38 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1765-1147T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683377 | |||||||
| chr3:158683467 | A | G | 2 | a0002c0002t0001g0086 a0002c0002t0001g0087 |
2 | HG02027.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1765-1057A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683467 | |||||||
| chr3:158683486 | A | G | 3 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0023g0306 |
3 | HG03041.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1765-1038A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683486 | |||||||
| chr3:158683505 | A | T | 23 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(20): Show |
24 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1765-1019A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683505 | |||||||
| chr3:158683512 | A | G | 6 | a0001c0001t0009g0289 a0001c0001t0009g0290 a0001c0001t0009g0291 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1765-1012A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683512 | |||||||
| chr3:158683556 | G | A | 2 | a0003c0003t0007g0248 a0003c0003t0007g0261 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1765-968G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683556 | |||||||
| chr3:158683584 | T | G | 1 | a0001c0001t0003g0189 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1765-940T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683584 | |||||||
| chr3:158683765 | A | T | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1765-759A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683765 | |||||||
| chr3:158684117 | C | G | 23 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(20): Show |
24 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1765-407C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684117 | |||||||
| chr3:158684146 | A | C | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1765-378A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684146 | |||||||
| chr3:158684171 | G | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1765-353G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684171 | |||||||
| chr3:158684184 | C | T | 1 | a0002c0002t0001g0144 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1765-340C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684184 | |||||||
| chr3:158684226 | A | G | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1765-298A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684226 | |||||||
| chr3:158684430 | C | T | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1765-94C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684430 | |||||||
| chr3:158684491 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1765-33C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684491 | |||||||
| chr3:158684799 | C | T | 6 | a0001c0001t0008g0262 a0001c0001t0008g0267 a0001c0001t0008g0269 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1909+131C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158684799 | |||||||
| chr3:158684900 | A | C | 3 | a0002c0002t0001g0097 a0002c0002t0001g0118 a0010c0014t0001g0094 |
3 | HG02109.hp2 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1909+232A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158684900 | |||||||
| chr3:158685002 | C | CTTG | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1909+336_1909+337i others(5): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158685002 | ||||||
| chr3:158685016 | C | G | 1 | a0001c0001t0004g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1909+348C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685016 | |||||||
| chr3:158685252 | G | T | 1 | a0001c0004t0025g0300 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1909+584G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685252 | |||||||
| chr3:158685405 | C | T | 1 | a0002c0002t0001g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1909+737C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685405 | |||||||
| chr3:158685529 | G | A | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1909+861G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685529 | |||||||
| chr3:158685583 | G | A | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1909+915G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685583 | |||||||
| chr3:158685596 | G | A | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1909+928G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685596 | |||||||
| chr3:158685696 | T | C | 28 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(25): Show |
38 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1909+1028T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685696 | |||||||
| chr3:158685710 | G | A | 1 | a0002c0002t0001g0112 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1909+1042G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685710 | |||||||
| chr3:158685750 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1909+1082G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685750 | |||||||
| chr3:158685823 | C | T | 1 | a0001c0001t0015g0016 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1909+1155C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685823 | |||||||
| chr3:158685941 | G | A | 1 | a0001c0001t0003g0214 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1909+1273G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685941 | |||||||
| chr3:158685961 | T | G | 5 | a0002c0002t0001g0011 a0002c0002t0001g0024 a0002c0002t0001g0154 others(2): Show |
8 | HG01346.hp1 HG01433.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1909+1293T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685961 | |||||||
| chr3:158686103 | T | C | 2 | a0001c0001t0004g0263 a0001c0001t0004g0276 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1909+1435T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686103 | |||||||
| chr3:158686155 | A | G | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1909+1487A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686155 | |||||||
| chr3:158686217 | G | T | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1909+1549G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686217 | |||||||
| chr3:158686397 | T | TA | 137 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(134): Show |
155 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1909+1736dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686397 | ||||||
| chr3:158686452 | C | G | 1 | a0001c0001t0003g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1909+1784C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686452 | |||||||
| chr3:158686478 | C | T | 201 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(198): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1909+1810C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686478 | |||||||
| chr3:158686551 | A | G | 3 | a0001c0001t0014g0178 a0001c0001t0014g0179 a0001c0001t0014g0296 |
3 | HG03098.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1909+1883A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686551 | |||||||
| chr3:158686651 | ATAT | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1909+1989_1909+199 others(7): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686651 | ||||||
| chr3:158686721 | G | GT | 69 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0031 others(66): Show |
84 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1909+2076dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686721 | ||||||
| chr3:158686721 | G | GTT | 29 | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0039 others(26): Show |
30 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1909+2075_1909+207 others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686721 | ||||||
| chr3:158686721 | G | GTTT | 71 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(68): Show |
77 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1909+2074_1909+207 others(7): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686721 | ||||||
| chr3:158686721 | G | GTTTT | 48 | a0001c0001t0003g0184 a0001c0001t0003g0186 a0001c0001t0003g0191 others(45): Show |
60 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1909+2073_1909+207 others(8): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686721 | ||||||
| chr3:158686721 | G | GTTTTT | 7 | a0001c0001t0004g0030 a0001c0001t0004g0180 a0001c0001t0004g0232 others(4): Show |
7 | HG02818.hp1 HG03486.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.1909+2072_1909+207 others(9): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686721 | ||||||
| chr3:158686721 | GT | G | 7 | a0002c0002t0001g0004 a0002c0002t0001g0092 a0002c0002t0001g0099 others(4): Show |
11 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1909+2076delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686721 | ||||||
| chr3:158686787 | C | T | 1 | a0001c0001t0003g0186 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1909+2119C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686787 | |||||||
| chr3:158686890 | G | A | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1909+2222G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686890 | |||||||
| chr3:158686969 | G | C | 52 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(49): Show |
63 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1909+2301G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686969 | |||||||
| chr3:158687029 | T | G | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1909+2361T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687029 | |||||||
| chr3:158687031 | C | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1909+2363C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687031 | |||||||
| chr3:158687036 | T | C | 2 | a0001c0001t0003g0191 a0001c0001t0003g0198 |
2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1909+2368T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687036 | |||||||
| chr3:158687086 | T | C | 1 | a0002c0002t0001g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1909+2418T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687086 | |||||||
| chr3:158687087 | C | T | 1 | a0002c0002t0001g0103 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1909+2419C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687087 | |||||||
| chr3:158687156 | C | T | 5 | a0003c0003t0007g0230 a0003c0003t0007g0247 a0003c0003t0007g0248 others(2): Show |
5 | HG01175.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909+2488C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687156 | |||||||
| chr3:158687216 | G | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1909+2548G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687216 | |||||||
| chr3:158687428 | C | T | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1910-2735C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687428 | |||||||
| chr3:158687615 | G | A | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1910-2548G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687615 | |||||||
| chr3:158687683 | G | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0042 |
2 | HG00140.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1910-2480G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687683 | |||||||
| chr3:158687694 | C | G | 1 | a0002c0002t0001g0112 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1910-2469C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687694 | |||||||
| chr3:158687720 | C | T | 1 | a0001c0001t0004g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1910-2443C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687720 | |||||||
| chr3:158687780 | A | G | 1 | a0002c0002t0001g0136 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1910-2383A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687780 | |||||||
| chr3:158687829 | G | A | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1910-2334G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687829 | |||||||
| chr3:158687907 | C | A | 8 | a0001c0001t0007g0255 a0003c0003t0007g0230 a0003c0003t0007g0235 others(5): Show |
8 | HG01175.hp1 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1910-2256C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687907 | |||||||
| chr3:158687916 | G | A | 28 | a0001c0001t0004g0002 a0001c0001t0004g0013 a0001c0001t0004g0014 others(25): Show |
38 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1910-2247G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687916 | |||||||
| chr3:158687925 | T | G | 12 | a0001c0001t0009g0289 a0001c0001t0009g0290 a0001c0001t0009g0291 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1910-2238T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687925 | |||||||
| chr3:158687941 | A | G | 7 | a0001c0001t0004g0029 a0001c0001t0004g0233 a0001c0001t0004g0244 others(4): Show |
8 | HG02257.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1910-2222A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687941 | |||||||
| chr3:158687977 | G | A | 115 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(112): Show |
132 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1910-2186G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687977 | |||||||
| chr3:158687986 | T | C | 23 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(20): Show |
24 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1910-2177T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687986 | |||||||
| chr3:158688084 | G | A | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1910-2079G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688084 | |||||||
| chr3:158688110 | A | G | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1910-2053A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688110 | |||||||
| chr3:158688167 | T | G | 1 | a0001c0001t0027g0236 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1910-1996T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688167 | |||||||
| chr3:158688190 | A | T | 1 | a0002c0002t0001g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1910-1973A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688190 | |||||||
| chr3:158688216 | C | T | 26 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(23): Show |
27 | HG01175.hp1 HG01243.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1910-1947C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688216 | |||||||
| chr3:158688257 | T | C | 2 | a0001c0001t0002g0049 a0001c0001t0002g0066 |
2 | HG02698.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1910-1906T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688257 | |||||||
| chr3:158688286 | G | A | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1910-1877G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688286 | |||||||
| chr3:158688385 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1910-1778G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688385 | |||||||
| chr3:158688672 | T | G | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1910-1491T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688672 | |||||||
| chr3:158688750 | A | C | 1 | a0001c0001t0018g0294 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1910-1413A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688750 | |||||||
| chr3:158688849 | G | T | 1 | a0002c0002t0001g0135 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1910-1314G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688849 | |||||||
| chr3:158688934 | G | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1910-1229G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688934 | |||||||
| chr3:158689126 | A | G | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1910-1037A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689126 | |||||||
| chr3:158689153 | T | C | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1910-1010T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689153 | |||||||
| chr3:158689397 | A | C | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1910-766A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689397 | |||||||
| chr3:158689442 | G | A | 1 | a0002c0002t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1910-721G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689442 | |||||||
| chr3:158689442 | G | T | 51 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(48): Show |
57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1910-721G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689442 | |||||||
| chr3:158689519 | A | G | 1 | a0002c0002t0001g0142 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1910-644A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689519 | |||||||
| chr3:158689544 | C | T | 141 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(138): Show |
159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1910-619C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689544 | |||||||
| chr3:158689581 | C | G | 1 | a0001c0001t0002g0039 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1910-582C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689581 | |||||||
| chr3:158689595 | C | T | 13 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1910-568C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689595 | |||||||
| chr3:158689641 | A | G | 202 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1910-522A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689641 | |||||||
| chr3:158689660 | C | T | 2 | a0002c0002t0001g0107 a0002c0002t0001g0109 |
2 | HG00639.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.1910-503C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689660 | |||||||
| chr3:158689728 | T | C | 2 | a0001c0001t0003g0192 a0001c0001t0003g0223 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1910-435T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689728 | |||||||
| chr3:158689747 | C | CA | 20 | a0001c0001t0003g0197 a0001c0001t0003g0215 a0001c0001t0009g0289 others(17): Show |
21 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1910-400dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158689747 | ||||||
| chr3:158689747 | CA | C | 60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0015 others(57): Show |
73 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1910-400delA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158689747 | ||||||
| chr3:158689976 | T | C | 1 | a0001c0001t0003g0195 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1910-187T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689976 | |||||||
| chr3:158690034 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1910-129G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158690034 | |||||||
| chr3:158690141 | CT | C | 7 | a0001c0001t0002g0053 a0001c0001t0003g0190 a0001c0001t0003g0210 others(4): Show |
7 | HG01069.hp1 NA18939.hp1 NA18962.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1910-8delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158690141 | ||||||
| chr3:158690334 | T | G | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2070+11T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158690334 | |||||||
| chr3:158690681 | T | A | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2070+358T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158690681 | |||||||
| chr3:158690836 | T | G | 1 | a0002c0002t0001g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2071-303T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158690836 | |||||||
| chr3:158690895 | G | A | 2 | a0001c0001t0002g0040 a0001c0001t0002g0075 |
2 | NA18992.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2071-244G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158690895 | |||||||
| chr3:158690914 | G | A | 1 | a0002c0002t0001g0163 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2071-225G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158690914 | |||||||
| chr3:158691090 | A | G | 1 | a0001c0001t0008g0270 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2071-49A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158691090 | |||||||
| chr3:158691119 | T | C | 1 | a0001c0001t0003g0196 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2071-20T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158691119 | |||||||
| chr3:158691122 | A | G | 6 | a0001c0001t0009g0289 a0001c0001t0009g0290 a0001c0001t0009g0291 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2071-17A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158691122 | |||||||
| chr3:158691304 | C | CA | 139 | a0001c0001t0003g0009 a0001c0001t0003g0012 a0001c0001t0003g0026 others(136): Show |
157 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.2125-26dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 158691304 | ||||||
| chr3:158691311 | C | A | 1 | a0001c0004t0026g0305 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2125-25C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 17/17 | chr3 | 158691311 |