Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 81577 |
| ensemblid | ENSG00000141098.13 |
| hgncid | 28159 |
| symbol | GFOD2 |
| name | Gfo/Idh/MocA-like oxidoreductase domain containing 2 |
| refseq_nuc | NM_030819.4 |
| refseq_prot | NP_110446.3 |
| ensembl_nuc | ENST00000268797.12 |
| ensembl_prot | ENSP00000268797.7 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 67674536 |
| end | 67719316 |
| strand | - |
| ver | v1.2 |
| region | chr16:67674536-67719316 |
| region5000 | chr16:67669536-67724316 |
| regionname0 | GFOD2_chr16_67674536_67719316 |
| regionname5000 | GFOD2_chr16_67669536_67724316 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1155 | 175 | 76 | 43 | 28 | 3 | 23 | GFOD2_chr16_67669536_67724316 | GFOD2 | ATGAA others(1150): Show |
chr16 | 67669536 | 67724316 | ||
| a0001c0002 | 0/0 | 1155 | 3 | 0 | 3 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | ATGAA others(1150): Show |
chr16 | 67669536 | 67724316 | ||
| a0001c0003 | 0/0 | 1155 | 3 | 0 | 0 | 0 | 0 | 3 | GFOD2_chr16_67669536_67724316 | GFOD2 | ATGAA others(1150): Show |
chr16 | 67669536 | 67724316 | ||
| a0001c0004 | 0/0 | 1155 | 2 | 0 | 1 | 0 | 1 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | ATGAA others(1150): Show |
chr16 | 67669536 | 67724316 | ||
| a0001c0005 | 0/0 | 1155 | 2 | 2 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | ATGAA others(1150): Show |
chr16 | 67669536 | 67724316 | ||
| a0001c0006 | 0/0 | 1155 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | ATGAA others(1150): Show |
chr16 | 67669536 | 67724316 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2018 | 91 | 25 | 25 | 20 | 2 | 18 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0001t0002 | 0/0 | 2018 | 76 | 46 | 17 | 8 | 1 | 4 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0001t0004 | 0/0 | 2018 | 2 | 2 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0001t0005 | 0/0 | 2018 | 2 | 1 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0001t0007 | 0/0 | 2018 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0001t0008 | 0/0 | 2018 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0001t0009 | 0/1 | 2018 | 1 | 0 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0001t0010 | 0/0 | 2018 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0002t0001 | 0/0 | 2018 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0002t0006 | 0/0 | 2018 | 2 | 0 | 2 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0003t0002 | 0/0 | 2018 | 3 | 0 | 0 | 0 | 0 | 3 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0004t0001 | 0/0 | 2018 | 2 | 0 | 1 | 0 | 1 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0005t0003 | 0/0 | 2018 | 2 | 2 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| a0001c0006t0002 | 0/0 | 2018 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | AGAAA others(2013): Show |
chr16 | 67669536 | 67724316 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 1 | 1 | 3 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0003 | 1/0 | 3 | 1 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0009g0168 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0001t0010g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0002t0006g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0004t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0005t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0005t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| a0001c0006t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01192 | hp1 | a0001 | c0006 | t0002 | g0125 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01358 | hp1 | a0001 | c0004 | t0001 | g0007 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01358 | hp2 | a0001 | c0002 | t0006 | g0009 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0131 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01496 | hp2 | a0001 | c0002 | t0006 | g0009 | AMR | CLM | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01884 | hp1 | a0001 | c0005 | t0003 | g0102 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02735 | hp2 | a0001 | c0001 | t0010 | g0169 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0132 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ESN | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ESN | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0128 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0067 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | ESN | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03516 | hp2 | a0001 | c0005 | t0003 | g0101 | AFR | ESN | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | GWD | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0139 | SAS | BEB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG04115 | hp2 | a0001 | c0003 | t0002 | g0142 | SAS | STU | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | STU | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0141 | SAS | STU | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | YRI | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | YRI | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | YRI | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | LWK | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | LWK | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | YRI | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | YRI | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ASW | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ASW | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | TSI | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA20752 | hp2 | a0001 | c0004 | t0001 | g0007 | EUR | TSI | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | MSL | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | USA | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | USA | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0168 | REF | REF | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | GFOD2_chr16_67669536_67724316 | GFOD2 | chr16 | 67669536 | 67724316 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67675296 | C | T | 1 | a0001c0003 | 3 | HG03927.hp1 HG04115.hp2 HG04204.hp2 |
synonymous_variant | LOW | c.1017G>A | p.Glu339Glu | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 3/3 | 1258/2018 | 1017/1158 | 339/385 | chr16 | 67675296 | |||
| chr16:67675359 | G | A | 1 | a0001c0004 | 2 | HG01358.hp1 NA20752.hp2 |
synonymous_variant | LOW | c.954C>T | p.Phe318Phe | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 3/3 | 1195/2018 | 954/1158 | 318/385 | chr16 | 67675359 | |||
| chr16:67675533 | G | A | 1 | a0001c0005 | 2 | HG01884.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.780C>T | p.Leu260Leu | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 3/3 | 1021/2018 | 780/1158 | 260/385 | chr16 | 67675533 | |||
| chr16:67675731 | G | C | 1 | a0001c0006 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.582C>G | p.Ala194Ala | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 3/3 | 823/2018 | 582/1158 | 194/385 | chr16 | 67675731 | |||
| chr16:67676052 | A | G | 1 | a0001c0002 | 3 | HG01358.hp2 HG01496.hp2 HG01952.hp1 |
splice_region_variant&synonymous_variant | LOW | c.261T>C | p.Gly87Gly | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 3/3 | 502/2018 | 261/1158 | 87/385 | chr16 | 67676052 | |||
| chr16:67685692 | G | A | 1 | a0001c0003 | 3 | HG03927.hp1 HG04115.hp2 HG04204.hp2 |
synonymous_variant | LOW | c.24C>T | p.Gly8Gly | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/3 | 265/2018 | 24/1158 | 8/385 | chr16 | 67685692 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67674550 | T | C | 1 | a0001c0001t0007 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*605A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 3/3 | 605 | chr16 | 67674550 | ||||||
| chr16:67674844 | C | T | 1 | a0001c0005t0003 | 2 | HG01884.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*311G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 3/3 | 311 | chr16 | 67674844 | ||||||
| chr16:67674954 | G | C | 1 | a0001c0001t0008 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*201C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 3/3 | 201 | chr16 | 67674954 | ||||||
| chr16:67674988 | G | A | 1 | a0001c0001t0004 | 2 | HG03209.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*167C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 3/3 | 167 | chr16 | 67674988 | ||||||
| chr16:67674994 | A | G | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(5): Show |
88 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*161T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 3/3 | 161 | chr16 | 67674994 | ||||||
| chr16:67675152 | G | A | 1 | a0001c0001t0005 | 2 | HG01433.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 3/3 | 3 | chr16 | 67675152 | ||||||
| chr16:67719259 | G | A | 1 | a0001c0002t0006 | 2 | HG01358.hp2 HG01496.hp2 |
5_prime_UTR_variant | MODIFIER | c.-184C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/3 | 33544 | chr16 | 67719259 | ||||||
| chr16:67719282 | G | A | 1 | a0001c0001t0010 | 1 | HG02735.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-207C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/3 | chr16 | 67719282 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67676148 | A | C | 1 | a0001c0001t0002g0154 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.260-95T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67676148 | |||||||
| chr16:67676155 | C | T | 3 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 |
3 | HG03041.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.260-102G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67676155 | |||||||
| chr16:67676166 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.260-113A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67676166 | |||||||
| chr16:67676278 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.260-225G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67676278 | |||||||
| chr16:67676300 | A | AT | 2 | a0001c0005t0003g0101 a0001c0005t0003g0102 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.260-248_260-247ins others(1): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67676300 | |||||||
| chr16:67676301 | A | T | 2 | a0001c0005t0003g0101 a0001c0005t0003g0102 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.260-248T>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67676301 | |||||||
| chr16:67676714 | T | C | 5 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG02622.hp1 HG02896.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-661A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67676714 | |||||||
| chr16:67676782 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0091 |
2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.260-729C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67676782 | |||||||
| chr16:67677104 | C | T | 1 | a0001c0001t0002g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.260-1051G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67677104 | |||||||
| chr16:67677172 | A | G | 6 | a0001c0001t0001g0028 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG01346.hp1 HG01928.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.260-1119T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67677172 | |||||||
| chr16:67677269 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.260-1216G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67677269 | |||||||
| chr16:67677270 | G | A | 8 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(5): Show |
8 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-1217C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67677270 | |||||||
| chr16:67677296 | C | T | 21 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
22 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.260-1243G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67677296 | |||||||
| chr16:67677362 | C | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-1309G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67677362 | |||||||
| chr16:67677901 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.260-1848C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67677901 | |||||||
| chr16:67678097 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0017 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.260-2044G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67678097 | |||||||
| chr16:67678115 | A | G | 86 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(83): Show |
88 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.260-2062T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67678115 | |||||||
| chr16:67678307 | T | C | 1 | a0001c0001t0005g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.260-2254A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67678307 | |||||||
| chr16:67678350 | C | T | 2 | a0001c0001t0005g0131 a0001c0001t0005g0132 |
2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.260-2297G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67678350 | |||||||
| chr16:67678433 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.260-2380C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67678433 | |||||||
| chr16:67678457 | C | T | 17 | a0001c0001t0002g0140 a0001c0001t0002g0146 a0001c0001t0002g0147 others(14): Show |
17 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.260-2404G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67678457 | |||||||
| chr16:67678463 | T | C | 86 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(83): Show |
88 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.260-2410A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67678463 | |||||||
| chr16:67678476 | C | CA | 38 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0017 others(35): Show |
39 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.260-2424dupT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67678476 | |||||||
| chr16:67678489 | A | AG | 3 | a0001c0001t0002g0021 a0001c0005t0003g0101 a0001c0005t0003g0102 |
3 | HG00741.hp1 HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.260-2437_260-2436i others(3): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67678489 | |||||||
| chr16:67678839 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.260-2786C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67678839 | |||||||
| chr16:67679102 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.260-3049C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67679102 | |||||||
| chr16:67679271 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.260-3218G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67679271 | |||||||
| chr16:67679271 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.260-3218G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67679271 | |||||||
| chr16:67679382 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.260-3329A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67679382 | |||||||
| chr16:67679698 | C | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0070 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.260-3645G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67679698 | |||||||
| chr16:67679878 | C | A | 2 | a0001c0005t0003g0101 a0001c0005t0003g0102 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.260-3825G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67679878 | |||||||
| chr16:67679897 | A | C | 28 | a0001c0001t0002g0008 a0001c0001t0002g0105 a0001c0001t0002g0111 others(25): Show |
29 | HG00438.hp2 HG01109.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.260-3844T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67679897 | |||||||
| chr16:67679909 | C | A | 1 | a0001c0001t0005g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.260-3856G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67679909 | |||||||
| chr16:67679912 | C | A | 14 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(11): Show |
15 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.260-3859G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67679912 | |||||||
| chr16:67679912 | C | CAAA | 8 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(5): Show |
8 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-3862_260-3860d others(5): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67679912 | |||||||
| chr16:67679915 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.260-3862T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67679915 | |||||||
| chr16:67680308 | G | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-4255C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67680308 | |||||||
| chr16:67680657 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
178 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.260-4604T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67680657 | |||||||
| chr16:67681155 | G | C | 1 | a0001c0001t0004g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.259+4302C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67681155 | |||||||
| chr16:67681382 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.259+4075C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67681382 | |||||||
| chr16:67681533 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.259+3924G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67681533 | |||||||
| chr16:67681534 | A | G | 86 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(83): Show |
88 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.259+3923T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67681534 | |||||||
| chr16:67681794 | G | A | 25 | a0001c0001t0002g0140 a0001c0001t0002g0143 a0001c0001t0002g0144 others(22): Show |
25 | HG01109.hp1 HG01884.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.259+3663C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67681794 | |||||||
| chr16:67681804 | CAG | C | 1 | a0001c0001t0001g0006 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.259+3651_259+3652d others(4): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67681804 | |||||||
| chr16:67681810 | C | T | 22 | a0001c0001t0002g0140 a0001c0001t0002g0143 a0001c0001t0002g0144 others(19): Show |
22 | HG01109.hp1 HG01884.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.259+3647G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67681810 | |||||||
| chr16:67681939 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.259+3518C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67681939 | |||||||
| chr16:67682069 | G | A | 2 | a0001c0005t0003g0101 a0001c0005t0003g0102 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.259+3388C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67682069 | |||||||
| chr16:67682099 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.259+3358C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67682099 | |||||||
| chr16:67682184 | C | T | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259+3273G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67682184 | |||||||
| chr16:67682212 | G | C | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259+3245C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67682212 | |||||||
| chr16:67682227 | G | A | 9 | a0001c0001t0002g0019 a0001c0001t0002g0133 a0001c0001t0002g0134 others(6): Show |
9 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.259+3230C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67682227 | |||||||
| chr16:67682244 | G | C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+3213C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67682244 | |||||||
| chr16:67682279 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.259+3178C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67682279 | |||||||
| chr16:67682397 | C | T | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259+3060G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67682397 | |||||||
| chr16:67683105 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.259+2352G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67683105 | |||||||
| chr16:67683190 | A | G | 1 | a0001c0001t0002g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.259+2267T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67683190 | |||||||
| chr16:67683361 | G | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+2096C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67683361 | |||||||
| chr16:67683569 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.259+1888G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67683569 | |||||||
| chr16:67683701 | G | A | 1 | a0001c0001t0002g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.259+1756C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67683701 | |||||||
| chr16:67683783 | G | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0008g0067 |
8 | HG00738.hp1 HG02723.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+1674C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67683783 | |||||||
| chr16:67684381 | T | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+1076A>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67684381 | |||||||
| chr16:67684406 | T | A | 2 | a0001c0001t0004g0099 a0001c0001t0004g0100 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.259+1051A>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67684406 | |||||||
| chr16:67684588 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.259+869A>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67684588 | |||||||
| chr16:67684591 | G | A | 2 | a0001c0001t0002g0150 a0001c0001t0002g0154 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.259+866C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67684591 | |||||||
| chr16:67684647 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.259+810C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67684647 | |||||||
| chr16:67684660 | A | C | 86 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(83): Show |
88 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.259+797T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67684660 | |||||||
| chr16:67684681 | A | G | 41 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(38): Show |
42 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.259+776T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67684681 | |||||||
| chr16:67684910 | T | A | 1 | a0001c0001t0001g0031 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.259+547A>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67684910 | |||||||
| chr16:67685281 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0167 |
3 | HG02451.hp2 HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.259+176G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 2/2 | chr16 | 67685281 | |||||||
| chr16:67685982 | C | T | 6 | a0001c0001t0002g0135 a0001c0001t0002g0159 a0001c0001t0002g0160 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-87-180G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67685982 | |||||||
| chr16:67686144 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-87-342C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67686144 | |||||||
| chr16:67686262 | C | T | 1 | a0001c0001t0002g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-87-460G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67686262 | |||||||
| chr16:67686529 | C | T | 2 | a0001c0001t0004g0099 a0001c0001t0004g0100 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-87-727G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67686529 | |||||||
| chr16:67686621 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-87-819C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67686621 | |||||||
| chr16:67686675 | CA | C | 41 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(38): Show |
42 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.-87-874delT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67686675 | |||||||
| chr16:67686911 | C | G | 3 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 |
3 | HG01884.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-87-1109G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67686911 | |||||||
| chr16:67686982 | A | G | 3 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0166 |
3 | HG02818.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-87-1180T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67686982 | |||||||
| chr16:67687008 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-87-1206A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67687008 | |||||||
| chr16:67687115 | T | A | 2 | a0001c0001t0002g0159 a0001c0001t0002g0160 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-87-1313A>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67687115 | |||||||
| chr16:67687147 | C | CA | 8 | a0001c0001t0002g0015 a0001c0001t0002g0143 a0001c0001t0002g0144 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-87-1346dupT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67687147 | |||||||
| chr16:67687284 | T | C | 2 | a0001c0001t0005g0131 a0001c0001t0005g0132 |
2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-87-1482A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67687284 | |||||||
| chr16:67687411 | C | T | 1 | a0001c0001t0002g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-87-1609G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67687411 | |||||||
| chr16:67687533 | C | T | 1 | a0001c0001t0002g0005 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-87-1731G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67687533 | |||||||
| chr16:67687620 | G | A | 13 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(10): Show |
14 | HG01099.hp1 HG01255.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.-87-1818C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67687620 | |||||||
| chr16:67687640 | CA | C | 32 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(29): Show |
33 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.-87-1839delT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67687640 | |||||||
| chr16:67687694 | G | T | 2 | a0001c0005t0003g0101 a0001c0005t0003g0102 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-87-1892C>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67687694 | |||||||
| chr16:67687808 | TA | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
149 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.-87-2007delT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67687808 | |||||||
| chr16:67687808 | TAA | T | 5 | a0001c0001t0001g0074 a0001c0001t0001g0089 a0001c0001t0001g0093 others(2): Show |
5 | HG01167.hp1 HG01256.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-87-2008_-87-2007d others(4): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67687808 | |||||||
| chr16:67687936 | C | G | 1 | a0001c0001t0002g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-87-2134G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67687936 | |||||||
| chr16:67688139 | G | C | 2 | a0001c0001t0002g0150 a0001c0001t0002g0154 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-87-2337C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688139 | |||||||
| chr16:67688242 | G | T | 1 | a0001c0001t0001g0076 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-87-2440C>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688242 | |||||||
| chr16:67688274 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-87-2472A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688274 | |||||||
| chr16:67688420 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-87-2618A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688420 | |||||||
| chr16:67688425 | T | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-2623A>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688425 | |||||||
| chr16:67688465 | G | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 |
3 | HG01884.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-87-2663C>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688465 | |||||||
| chr16:67688656 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-87-2854G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688656 | |||||||
| chr16:67688734 | C | CT | 42 | a0001c0001t0001g0167 a0001c0001t0002g0008 a0001c0001t0002g0010 others(39): Show |
43 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.-87-2933dupA | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688734 | |||||||
| chr16:67688734 | C | T | 1 | a0001c0001t0007g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-87-2932G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688734 | |||||||
| chr16:67688887 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-87-3085G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688887 | |||||||
| chr16:67688941 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-87-3139C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688941 | |||||||
| chr16:67688966 | C | T | 37 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(34): Show |
38 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.-87-3164G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688966 | |||||||
| chr16:67688981 | T | C | 86 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(83): Show |
88 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.-87-3179A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67688981 | |||||||
| chr16:67689167 | T | C | 17 | a0001c0001t0002g0140 a0001c0001t0002g0146 a0001c0001t0002g0147 others(14): Show |
17 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-87-3365A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67689167 | |||||||
| chr16:67689420 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-87-3618G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67689420 | |||||||
| chr16:67689622 | G | C | 2 | a0001c0001t0004g0099 a0001c0001t0004g0100 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-87-3820C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67689622 | |||||||
| chr16:67689650 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-87-3848C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67689650 | |||||||
| chr16:67689898 | T | C | 37 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(34): Show |
38 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.-87-4096A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67689898 | |||||||
| chr16:67690398 | A | AT | 16 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0035 others(13): Show |
17 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-87-4597dupA | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67690398 | |||||||
| chr16:67690398 | A | T | 1 | a0001c0001t0002g0022 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-87-4596T>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67690398 | |||||||
| chr16:67690656 | C | A | 1 | a0001c0002t0006g0009 | 2 | HG01358.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-87-4854G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67690656 | |||||||
| chr16:67690708 | C | G | 1 | a0001c0001t0002g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-87-4906G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67690708 | |||||||
| chr16:67690830 | A | G | 1 | a0001c0001t0002g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-87-5028T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67690830 | |||||||
| chr16:67690954 | T | C | 86 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(83): Show |
88 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.-87-5152A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67690954 | |||||||
| chr16:67690987 | C | T | 20 | a0001c0001t0002g0140 a0001c0001t0002g0143 a0001c0001t0002g0144 others(17): Show |
20 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.-87-5185G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67690987 | |||||||
| chr16:67691444 | C | G | 86 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(83): Show |
88 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.-87-5642G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67691444 | |||||||
| chr16:67691508 | A | AC | 14 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(11): Show |
15 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-87-5707dupG | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67691508 | |||||||
| chr16:67691508 | A | ACC | 10 | a0001c0001t0002g0019 a0001c0001t0002g0133 a0001c0001t0002g0134 others(7): Show |
10 | HG01433.hp2 HG02622.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-87-5708_-87-5707d others(4): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67691508 | |||||||
| chr16:67691510 | C | A | 3 | a0001c0003t0002g0139 a0001c0003t0002g0141 a0001c0003t0002g0142 |
3 | HG03927.hp1 HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-87-5708G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67691510 | |||||||
| chr16:67691510 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-87-5708G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67691510 | |||||||
| chr16:67691511 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-87-5709G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67691511 | |||||||
| chr16:67691515 | C | A | 1 | a0001c0001t0001g0041 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-87-5713G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67691515 | |||||||
| chr16:67691517 | CA | C | 9 | a0001c0001t0001g0051 a0001c0001t0001g0078 a0001c0001t0001g0083 others(6): Show |
10 | HG01358.hp1 HG01496.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-87-5716delT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67691517 | |||||||
| chr16:67691518 | A | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0074 others(36): Show |
40 | HG00609.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-87-5716T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67691518 | |||||||
| chr16:67691519 | A | C | 18 | a0001c0001t0002g0140 a0001c0001t0002g0146 a0001c0001t0002g0147 others(15): Show |
18 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-87-5717T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67691519 | |||||||
| chr16:67691520 | A | C | 1 | a0001c0001t0002g0154 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-87-5718T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67691520 | |||||||
| chr16:67691959 | T | A | 1 | a0001c0001t0001g0030 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-87-6157A>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67691959 | |||||||
| chr16:67692228 | T | TA | 23 | a0001c0001t0001g0052 a0001c0001t0002g0016 a0001c0001t0002g0017 others(20): Show |
23 | HG01109.hp1 HG01884.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.-87-6427dupT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67692228 | |||||||
| chr16:67692309 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-87-6507G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67692309 | |||||||
| chr16:67692311 | G | GTGGCTCA | 41 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(38): Show |
42 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-87-6516_-87-6510d others(9): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67692311 | |||||||
| chr16:67692320 | G | A | 2 | a0001c0001t0002g0150 a0001c0001t0002g0154 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-87-6518C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67692320 | |||||||
| chr16:67692844 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-87-7042C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67692844 | |||||||
| chr16:67692846 | A | G | 1 | a0001c0001t0002g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-87-7044T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67692846 | |||||||
| chr16:67693048 | A | T | 1 | a0001c0001t0002g0145 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-87-7246T>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67693048 | |||||||
| chr16:67693166 | A | G | 19 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
25 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.-87-7364T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67693166 | |||||||
| chr16:67693249 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-87-7447G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67693249 | |||||||
| chr16:67693285 | G | GT | 15 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0019 others(12): Show |
15 | HG01070.hp2 HG01433.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-87-7484dupA | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67693285 | |||||||
| chr16:67693285 | G | GTT | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0022 others(1): Show |
5 | HG01070.hp1 HG01071.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-7485_-87-7484d others(4): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67693285 | |||||||
| chr16:67693562 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-87-7760C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67693562 | |||||||
| chr16:67693863 | T | G | 1 | a0001c0001t0004g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-87-8061A>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67693863 | |||||||
| chr16:67693934 | AAAAC | A | 5 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-8136_-87-8133d others(6): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67693934 | |||||||
| chr16:67694239 | C | T | 1 | a0001c0001t0005g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-87-8437G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67694239 | |||||||
| chr16:67694466 | T | A | 11 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(8): Show |
12 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-87-8664A>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67694466 | |||||||
| chr16:67694507 | C | T | 2 | a0001c0001t0004g0099 a0001c0001t0004g0100 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-87-8705G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67694507 | |||||||
| chr16:67694551 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0057 |
2 | HG01952.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-87-8749G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67694551 | |||||||
| chr16:67694646 | C | T | 1 | a0001c0001t0004g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-87-8844G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67694646 | |||||||
| chr16:67694987 | C | CT | 8 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG00609.hp2 HG01496.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-87-9186dupA | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67694987 | |||||||
| chr16:67694987 | CT | C | 7 | a0001c0001t0001g0029 a0001c0001t0001g0066 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-87-9186delA | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67694987 | |||||||
| chr16:67694987 | CTTTTTT | C | 17 | a0001c0001t0002g0140 a0001c0001t0002g0146 a0001c0001t0002g0147 others(14): Show |
17 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-87-9191_-87-9186d others(8): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67694987 | |||||||
| chr16:67694987 | CTTTTTTT | C | 15 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(12): Show |
16 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-87-9192_-87-9186d others(9): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67694987 | |||||||
| chr16:67695032 | G | A | 1 | a0001c0001t0008g0067 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-87-9230C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67695032 | |||||||
| chr16:67695038 | G | A | 1 | a0001c0001t0007g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-87-9236C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67695038 | |||||||
| chr16:67695086 | C | T | 3 | a0001c0001t0002g0108 a0001c0001t0002g0119 a0001c0001t0002g0137 |
3 | HG02809.hp1 HG02896.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-87-9284G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67695086 | |||||||
| chr16:67695212 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0049 |
2 | HG01109.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-87-9410C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67695212 | |||||||
| chr16:67695426 | T | TTACTG | 22 | a0001c0001t0002g0140 a0001c0001t0002g0143 a0001c0001t0002g0144 others(19): Show |
22 | HG01109.hp1 HG01884.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.-87-9625_-87-9624i others(7): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67695426 | |||||||
| chr16:67695427 | C | T | 22 | a0001c0001t0002g0140 a0001c0001t0002g0143 a0001c0001t0002g0144 others(19): Show |
22 | HG01109.hp1 HG01884.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.-87-9625G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67695427 | |||||||
| chr16:67695473 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-87-9671C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67695473 | |||||||
| chr16:67695534 | G | GT | 32 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0031 others(29): Show |
32 | HG00609.hp2 HG01109.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.-87-9733dupA | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67695534 | |||||||
| chr16:67695658 | C | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 |
3 | HG01884.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-87-9856G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67695658 | |||||||
| chr16:67695767 | C | T | 4 | a0001c0001t0002g0153 a0001c0001t0002g0155 a0001c0001t0002g0156 others(1): Show |
4 | HG02451.hp1 HG02647.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-87-9965G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67695767 | |||||||
| chr16:67696260 | G | A | 1 | a0001c0004t0001g0007 | 2 | HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-87-10458C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67696260 | |||||||
| chr16:67696510 | G | A | 3 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 |
3 | HG01884.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-87-10708C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67696510 | |||||||
| chr16:67696604 | G | C | 17 | a0001c0001t0002g0140 a0001c0001t0002g0146 a0001c0001t0002g0147 others(14): Show |
17 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-87-10802C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67696604 | |||||||
| chr16:67696618 | C | T | 20 | a0001c0001t0002g0140 a0001c0001t0002g0143 a0001c0001t0002g0144 others(17): Show |
20 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.-87-10816G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67696618 | |||||||
| chr16:67696715 | C | T | 29 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
30 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.-87-10913G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67696715 | |||||||
| chr16:67697075 | A | G | 2 | a0001c0005t0003g0101 a0001c0005t0003g0102 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-87-11273T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67697075 | |||||||
| chr16:67697301 | A | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-11499T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67697301 | |||||||
| chr16:67697917 | G | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-12115C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67697917 | |||||||
| chr16:67698283 | C | T | 41 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(38): Show |
42 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-87-12481G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67698283 | |||||||
| chr16:67698731 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-87-12929C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67698731 | |||||||
| chr16:67699069 | G | A | 3 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 |
3 | HG03041.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-87-13267C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699069 | |||||||
| chr16:67699113 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-87-13311G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699113 | |||||||
| chr16:67699114 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-87-13312C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699114 | |||||||
| chr16:67699117 | C | A | 37 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(34): Show |
38 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.-87-13315G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699117 | |||||||
| chr16:67699210 | T | C | 41 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(38): Show |
42 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.-87-13408A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699210 | |||||||
| chr16:67699334 | C | T | 37 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(34): Show |
38 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.-87-13532G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699334 | |||||||
| chr16:67699419 | G | A | 41 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(38): Show |
42 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-87-13617C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699419 | |||||||
| chr16:67699458 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-87-13656A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699458 | |||||||
| chr16:67699483 | T | C | 4 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-87-13681A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699483 | |||||||
| chr16:67699495 | T | C | 3 | a0001c0001t0002g0008 a0001c0001t0002g0105 a0001c0001t0002g0136 |
4 | NA18940.hp1 NA18991.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-87-13693A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699495 | |||||||
| chr16:67699603 | C | A | 1 | a0001c0001t0002g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-87-13801G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699603 | |||||||
| chr16:67699630 | T | C | 2 | a0001c0001t0002g0033 a0001c0001t0002g0129 |
2 | HG02602.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-87-13828A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699630 | |||||||
| chr16:67699839 | C | T | 4 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-87-14037G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699839 | |||||||
| chr16:67699985 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-87-14183C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67699985 | |||||||
| chr16:67700110 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-87-14308T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67700110 | |||||||
| chr16:67700648 | G | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-14846C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67700648 | |||||||
| chr16:67700651 | G | C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-14849C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67700651 | |||||||
| chr16:67700652 | C | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-14850G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67700652 | |||||||
| chr16:67700653 | A | C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-14851T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67700653 | |||||||
| chr16:67700654 | GTGA | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-14855_-87-1485 others(7): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67700654 | |||||||
| chr16:67700893 | C | T | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-87-15091G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67700893 | |||||||
| chr16:67700972 | G | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-15170C>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67700972 | |||||||
| chr16:67701036 | C | CA | 21 | a0001c0001t0001g0036 a0001c0001t0001g0049 a0001c0001t0002g0005 others(18): Show |
22 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-87-15235dupT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67701036 | |||||||
| chr16:67701036 | CA | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0056 others(2): Show |
5 | HG01256.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-15235delT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67701036 | |||||||
| chr16:67701096 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-87-15294C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67701096 | |||||||
| chr16:67701214 | T | C | 2 | a0001c0001t0002g0150 a0001c0001t0002g0154 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-87-15412A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67701214 | |||||||
| chr16:67701434 | T | C | 2 | a0001c0001t0002g0150 a0001c0001t0002g0154 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-87-15632A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67701434 | |||||||
| chr16:67701492 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0050 |
2 | HG00597.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-87-15690C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67701492 | |||||||
| chr16:67701785 | T | TA | 6 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(3): Show |
7 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-87-15984dupT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67701785 | |||||||
| chr16:67701785 | TA | T | 12 | a0001c0001t0001g0029 a0001c0001t0001g0055 a0001c0001t0001g0088 others(9): Show |
12 | HG01070.hp2 HG02622.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.-87-15984delT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67701785 | |||||||
| chr16:67702028 | G | A | 8 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(5): Show |
8 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-87-16226C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702028 | |||||||
| chr16:67702227 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-87-16425A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702227 | |||||||
| chr16:67702272 | C | T | 2 | a0001c0005t0003g0101 a0001c0005t0003g0102 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-87-16470G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702272 | |||||||
| chr16:67702398 | T | C | 1 | a0001c0001t0002g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-87-16596A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702398 | |||||||
| chr16:67702456 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0096 a0001c0001t0001g0158 |
3 | HG00597.hp2 NA18964.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-87-16654T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702456 | |||||||
| chr16:67702573 | TGTCATGA others(1): Show |
T | 4 | a0001c0001t0002g0008 a0001c0001t0002g0105 a0001c0001t0002g0111 others(1): Show |
5 | HG00438.hp2 NA18940.hp1 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.-88+16582_-88+1658 others(12): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702573 | |||||||
| chr16:67702592 | A | AT | 20 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0041 others(17): Show |
20 | HG00597.hp1 HG00741.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.-88+16570dupA | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702592 | |||||||
| chr16:67702592 | ATTT | A | 20 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(17): Show |
21 | HG01070.hp1 HG01071.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.-88+16568_-88+1657 others(7): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702592 | |||||||
| chr16:67702592 | ATTTTTTT others(3): Show |
A | 17 | a0001c0001t0002g0140 a0001c0001t0002g0146 a0001c0001t0002g0147 others(14): Show |
17 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-88+16561_-88+1657 others(14): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702592 | |||||||
| chr16:67702678 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-88+16485G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702678 | |||||||
| chr16:67702708 | T | G | 42 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(39): Show |
43 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.-88+16455A>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702708 | |||||||
| chr16:67702784 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-88+16379C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702784 | |||||||
| chr16:67702859 | A | C | 2 | a0001c0001t0004g0099 a0001c0001t0004g0100 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-88+16304T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702859 | |||||||
| chr16:67702937 | A | T | 15 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(12): Show |
16 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-88+16226T>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67702937 | |||||||
| chr16:67703116 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-88+16047A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67703116 | |||||||
| chr16:67703319 | C | G | 1 | a0001c0001t0002g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-88+15844G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67703319 | |||||||
| chr16:67703359 | C | T | 2 | a0001c0001t0002g0150 a0001c0001t0002g0154 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-88+15804G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67703359 | |||||||
| chr16:67703382 | A | C | 42 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(39): Show |
43 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.-88+15781T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67703382 | |||||||
| chr16:67703434 | G | GA | 17 | a0001c0001t0001g0096 a0001c0001t0002g0005 a0001c0001t0002g0019 others(14): Show |
18 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-88+15728dupT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67703434 | |||||||
| chr16:67703443 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-88+15720T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67703443 | |||||||
| chr16:67703630 | C | T | 17 | a0001c0001t0002g0140 a0001c0001t0002g0146 a0001c0001t0002g0147 others(14): Show |
17 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-88+15533G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67703630 | |||||||
| chr16:67703870 | C | A | 1 | a0001c0001t0002g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-88+15293G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67703870 | |||||||
| chr16:67704065 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-88+15098A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67704065 | |||||||
| chr16:67704347 | G | C | 2 | a0001c0001t0002g0150 a0001c0001t0002g0154 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-88+14816C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67704347 | |||||||
| chr16:67704647 | A | C | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-88+14516T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67704647 | |||||||
| chr16:67704722 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-88+14441G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67704722 | |||||||
| chr16:67704785 | T | A | 1 | a0001c0001t0002g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-88+14378A>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67704785 | |||||||
| chr16:67705433 | C | G | 1 | a0001c0001t0002g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-88+13730G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67705433 | |||||||
| chr16:67705507 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-88+13656G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67705507 | |||||||
| chr16:67705758 | G | A | 2 | a0001c0001t0004g0099 a0001c0001t0004g0100 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-88+13405C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67705758 | |||||||
| chr16:67705950 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-88+13213T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67705950 | |||||||
| chr16:67705977 | A | AT | 49 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(46): Show |
49 | HG00438.hp1 HG00609.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.-88+13185dupA | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67705977 | |||||||
| chr16:67706000 | G | T | 1 | a0001c0001t0004g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-88+13163C>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67706000 | |||||||
| chr16:67706049 | C | G | 1 | a0001c0001t0002g0120 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-88+13114G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67706049 | |||||||
| chr16:67706121 | C | A | 1 | a0001c0001t0002g0138 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-88+13042G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67706121 | |||||||
| chr16:67706173 | C | T | 22 | a0001c0001t0002g0140 a0001c0001t0002g0143 a0001c0001t0002g0144 others(19): Show |
22 | HG01109.hp1 HG01884.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.-88+12990G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67706173 | |||||||
| chr16:67706221 | C | T | 1 | a0001c0003t0002g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-88+12942G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67706221 | |||||||
| chr16:67706639 | T | C | 17 | a0001c0001t0002g0140 a0001c0001t0002g0146 a0001c0001t0002g0147 others(14): Show |
17 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-88+12524A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67706639 | |||||||
| chr16:67706683 | T | C | 3 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 |
3 | HG03041.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-88+12480A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67706683 | |||||||
| chr16:67707046 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-88+12117C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67707046 | |||||||
| chr16:67707058 | C | CA | 27 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0039 others(24): Show |
29 | HG01099.hp2 HG01109.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.-88+12104dupT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67707058 | |||||||
| chr16:67707176 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-88+11987A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67707176 | |||||||
| chr16:67707763 | C | T | 2 | a0001c0001t0004g0099 a0001c0001t0004g0100 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-88+11400G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67707763 | |||||||
| chr16:67707770 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-88+11393G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67707770 | |||||||
| chr16:67707853 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-88+11310C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67707853 | |||||||
| chr16:67708327 | T | C | 9 | a0001c0001t0002g0019 a0001c0001t0002g0133 a0001c0001t0002g0134 others(6): Show |
9 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-88+10836A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67708327 | |||||||
| chr16:67708338 | G | A | 8 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(5): Show |
8 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-88+10825C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67708338 | |||||||
| chr16:67708423 | G | A | 42 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(39): Show |
43 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.-88+10740C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67708423 | |||||||
| chr16:67709196 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-88+9967T>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67709196 | |||||||
| chr16:67709521 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-88+9642C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67709521 | |||||||
| chr16:67709660 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-88+9503C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67709660 | |||||||
| chr16:67709995 | G | C | 2 | a0001c0001t0002g0150 a0001c0001t0002g0154 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-88+9168C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67709995 | |||||||
| chr16:67710070 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-88+9093G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67710070 | |||||||
| chr16:67710329 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-88+8834C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67710329 | |||||||
| chr16:67710389 | C | CTTTG | 46 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(43): Show |
47 | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.-88+8770_-88+8773d others(6): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67710389 | |||||||
| chr16:67710452 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-88+8711G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67710452 | |||||||
| chr16:67710720 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-88+8443G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67710720 | |||||||
| chr16:67710862 | C | G | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-88+8301G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67710862 | |||||||
| chr16:67710955 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-88+8208A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67710955 | |||||||
| chr16:67711856 | T | A | 1 | a0001c0001t0002g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-88+7307A>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67711856 | |||||||
| chr16:67711935 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-88+7228A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67711935 | |||||||
| chr16:67712018 | C | T | 2 | a0001c0001t0002g0159 a0001c0001t0002g0160 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-88+7145G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712018 | |||||||
| chr16:67712256 | GCTCCCT | G | 15 | a0001c0001t0002g0140 a0001c0001t0002g0146 a0001c0001t0002g0147 others(12): Show |
15 | HG01109.hp1 HG02559.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.-88+6901_-88+6906d others(8): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712256 | |||||||
| chr16:67712262 | T | TCTCCCTC others(24): Show |
1 | a0001c0001t0004g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-88+6870_-88+6900d others(33): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712262 | |||||||
| chr16:67712268 | TCTCCCTC others(5): Show |
T | 1 | a0001c0001t0002g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-88+6883_-88+6894d others(14): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712268 | |||||||
| chr16:67712271 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-88+6892G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712271 | |||||||
| chr16:67712274 | T | C | 1 | a0001c0003t0002g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-88+6889A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712274 | |||||||
| chr16:67712274 | TCTCCCC | T | 21 | a0001c0001t0001g0096 a0001c0001t0002g0005 a0001c0001t0002g0019 others(18): Show |
22 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-88+6883_-88+6888d others(8): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712274 | |||||||
| chr16:67712280 | C | CCTCCCCC others(19): Show |
1 | a0001c0001t0004g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-88+6882_-88+6883i others(28): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712280 | |||||||
| chr16:67712280 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-88+6883G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712280 | |||||||
| chr16:67712299 | CT | C | 2 | a0001c0001t0002g0017 a0001c0001t0002g0098 |
2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-88+6863delA | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712299 | |||||||
| chr16:67712300 | T | C | 1 | a0001c0001t0002g0016 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-88+6863A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712300 | |||||||
| chr16:67712302 | T | C | 4 | a0001c0001t0002g0146 a0001c0001t0002g0164 a0001c0001t0002g0165 others(1): Show |
4 | HG02809.hp2 HG02818.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-88+6861A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712302 | |||||||
| chr16:67712458 | G | GT | 13 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(10): Show |
14 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(11): Show |
intron_variant | MODIFIER | c.-88+6704dupA | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712458 | |||||||
| chr16:67712540 | C | G | 1 | a0001c0001t0004g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-88+6623G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712540 | |||||||
| chr16:67712577 | G | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
4 | HG02109.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-88+6586C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712577 | |||||||
| chr16:67712630 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-88+6533G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712630 | |||||||
| chr16:67712701 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-88+6462C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712701 | |||||||
| chr16:67712704 | A | AC | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0082 others(3): Show |
6 | HG01099.hp1 HG01496.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-88+6458dupG | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712704 | |||||||
| chr16:67712708 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-88+6455G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712708 | |||||||
| chr16:67712708 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-88+6455G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712708 | |||||||
| chr16:67712769 | T | TC | 3 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0098 |
3 | HG01884.hp2 HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-88+6393dupG | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712769 | |||||||
| chr16:67712811 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-88+6352G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712811 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7658): Show |
1 | a0001c0001t0002g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7667): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7710): Show |
1 | a0001c0001t0002g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7719): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7705): Show |
1 | a0001c0001t0002g0105 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7714): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7695): Show |
1 | a0001c0001t0002g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7704): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7697): Show |
1 | a0001c0001t0002g0097 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7706): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7704): Show |
1 | a0001c0001t0002g0110 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7713): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7706): Show |
1 | a0001c0001t0002g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7715): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(8078): Show |
1 | a0001c0005t0003g0101 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(8087): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7700): Show |
3 | a0001c0001t0002g0008 a0001c0001t0002g0111 a0001c0001t0002g0136 |
4 | HG00438.hp2 NA18940.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7709): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7701): Show |
1 | a0001c0001t0002g0022 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7710): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(8077): Show |
1 | a0001c0005t0003g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(8086): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7700): Show |
1 | a0001c0001t0002g0124 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7709): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
1 | a0001c0001t0002g0106 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
3 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0138 |
3 | HG02071.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
1 | a0001c0001t0002g0146 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
1 | a0001c0001t0002g0151 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
1 | a0001c0001t0002g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7706): Show |
1 | a0001c0001t0002g0010 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7715): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7700): Show |
1 | a0001c0006t0002g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7709): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
1 | a0001c0001t0002g0108 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
1 | a0001c0001t0002g0021 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
1 | a0001c0001t0002g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
1 | a0001c0001t0002g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
2 | a0001c0001t0002g0122 a0001c0001t0002g0123 |
2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
2 | a0001c0001t0002g0129 a0001c0001t0007g0128 |
2 | HG03209.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
10 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(7): Show |
10 | HG01167.hp2 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
1 | a0001c0001t0002g0104 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
1 | a0001c0001t0002g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
1 | a0001c0001t0004g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
1 | a0001c0003t0002g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7693): Show |
1 | a0001c0003t0002g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7702): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
7 | a0001c0001t0002g0140 a0001c0001t0002g0147 a0001c0001t0002g0148 others(4): Show |
7 | HG01109.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
1 | a0001c0001t0002g0152 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
3 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0166 |
3 | HG02818.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7696): Show |
1 | a0001c0003t0002g0141 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7705): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7695): Show |
1 | a0001c0001t0002g0017 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7704): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7695): Show |
1 | a0001c0001t0002g0016 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7704): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7697): Show |
1 | a0001c0001t0002g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7706): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
1 | a0001c0001t0002g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
7 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(4): Show |
7 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
1 | a0001c0001t0002g0005 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
1 | a0001c0001t0004g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
1 | a0001c0001t0002g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7697): Show |
2 | a0001c0001t0002g0014 a0001c0001t0002g0120 |
2 | HG01255.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7706): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7697): Show |
1 | a0001c0001t0002g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7706): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7696): Show |
1 | a0001c0001t0010g0169 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7705): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7701): Show |
1 | a0001c0001t0002g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7710): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7700): Show |
1 | a0001c0001t0002g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7709): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7699): Show |
1 | a0001c0001t0002g0145 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7708): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7692): Show |
1 | a0001c0001t0002g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7701): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7690): Show |
1 | a0001c0001t0002g0154 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7699): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7698): Show |
1 | a0001c0001t0005g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7707): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712970 | G | GCCGCAGC others(7697): Show |
1 | a0001c0001t0005g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-88+6192_-88+6193i others(7706): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712970 | |||||||
| chr16:67712972 | G | T | 86 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(83): Show |
88 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.-88+6191C>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712972 | |||||||
| chr16:67712974 | T | C | 86 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(83): Show |
88 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.-88+6189A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712974 | |||||||
| chr16:67712977 | A | G | 86 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(83): Show |
88 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.-88+6186T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67712977 | |||||||
| chr16:67713082 | C | T | 2 | a0001c0001t0002g0150 a0001c0001t0002g0154 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-88+6081G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67713082 | |||||||
| chr16:67713378 | C | G | 2 | a0001c0001t0004g0099 a0001c0001t0004g0100 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-88+5785G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67713378 | |||||||
| chr16:67713403 | C | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0032 others(17): Show |
26 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.-88+5760G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67713403 | |||||||
| chr16:67713661 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-88+5502T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67713661 | |||||||
| chr16:67713829 | A | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0098 |
3 | HG01884.hp2 HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-88+5334T>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67713829 | |||||||
| chr16:67714195 | AGAGGCCA others(60): Show |
A | 2 | a0001c0001t0002g0150 a0001c0001t0002g0154 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-88+4901_-88+4967d others(69): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67714195 | |||||||
| chr16:67714440 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-88+4723A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67714440 | |||||||
| chr16:67714473 | C | CAA | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-88+4688_-88+4689d others(4): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67714473 | |||||||
| chr16:67714473 | CA | C | 7 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(4): Show |
7 | HG00609.hp2 HG01070.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-88+4689delT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67714473 | |||||||
| chr16:67714692 | G | A | 2 | a0001c0003t0002g0141 a0001c0003t0002g0142 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-88+4471C>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67714692 | |||||||
| chr16:67714703 | C | A | 1 | a0001c0001t0002g0018 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-88+4460G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67714703 | |||||||
| chr16:67715215 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-88+3948G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67715215 | |||||||
| chr16:67715395 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-88+3768G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67715395 | |||||||
| chr16:67715434 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-88+3729G>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67715434 | |||||||
| chr16:67715475 | G | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-88+3688C>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67715475 | |||||||
| chr16:67715835 | C | CA | 13 | a0001c0001t0002g0019 a0001c0001t0002g0133 a0001c0001t0002g0134 others(10): Show |
13 | HG01433.hp2 HG02622.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-88+3327dupT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67715835 | |||||||
| chr16:67715835 | CA | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG00597.hp1 HG00597.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-88+3327delT | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67715835 | |||||||
| chr16:67715891 | C | T | 17 | a0001c0001t0002g0140 a0001c0001t0002g0146 a0001c0001t0002g0147 others(14): Show |
17 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-88+3272G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67715891 | |||||||
| chr16:67716637 | C | T | 1 | a0001c0001t0002g0145 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-88+2526G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67716637 | |||||||
| chr16:67716766 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-88+2397A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67716766 | |||||||
| chr16:67717476 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-88+1687C>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67717476 | |||||||
| chr16:67717790 | C | CGATA | 58 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(55): Show |
60 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-88+1369_-88+1372d others(6): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67717790 | |||||||
| chr16:67717790 | C | CGATAGAT others(1): Show |
2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-88+1365_-88+1372d others(10): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67717790 | |||||||
| chr16:67717790 | C | CGATAGAT others(9): Show |
7 | a0001c0001t0002g0016 a0001c0001t0002g0140 a0001c0001t0002g0143 others(4): Show |
7 | HG02257.hp1 HG03041.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-88+1357_-88+1372d others(18): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67717790 | |||||||
| chr16:67717790 | C | CGATAGAT others(13): Show |
10 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0145 others(7): Show |
10 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-88+1353_-88+1372d others(22): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67717790 | |||||||
| chr16:67717790 | C | CGATAGAT others(17): Show |
5 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0153 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-88+1349_-88+1372d others(26): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67717790 | |||||||
| chr16:67717790 | C | CGATAGAT others(21): Show |
3 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 |
3 | HG02647.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-88+1372_-88+1373i others(30): Show |
GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67717790 | |||||||
| chr16:67717813 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-88+1350A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67717813 | |||||||
| chr16:67718059 | T | C | 5 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG02622.hp1 HG02896.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-88+1104A>G | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67718059 | |||||||
| chr16:67718379 | A | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0021 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-88+784T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67718379 | |||||||
| chr16:67718589 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-88+574T>C | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67718589 | |||||||
| chr16:67718812 | C | A | 3 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0166 |
3 | HG02818.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-88+351G>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67718812 | |||||||
| chr16:67718947 | C | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 |
3 | HG01884.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-88+216G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67718947 | |||||||
| chr16:67718992 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-88+171A>T | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67718992 | |||||||
| chr16:67719118 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(3): Show |
6 | HG01099.hp1 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-88+45G>A | GFOD2 | ENSG00000141098.13 | transcript | ENST00000268797.12 | protein_coding | 1/2 | chr16 | 67719118 |