Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2673 |
| ensemblid | ENSG00000198380.13 |
| hgncid | 4241 |
| symbol | GFPT1 |
| name | glutamine--fructose-6-phosphate transaminase 1 |
| refseq_nuc | NM_001244710.2 |
| refseq_prot | NP_001231639.1 |
| ensembl_nuc | ENST00000357308.9 |
| ensembl_prot | ENSP00000349860.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 69319780 |
| end | 69387227 |
| strand | - |
| ver | v1.2 |
| region | chr2:69319780-69387227 |
| region5000 | chr2:69314780-69392227 |
| regionname0 | GFPT1_chr2_69319780_69387227 |
| regionname5000 | GFPT1_chr2_69314780_69392227 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 699 | 365 | 90 | 58 | 169 | 10 | 36 | 127 | GFPT1_chr2_69314780_69392227 | GFPT1 | MCGIF others(694): Show |
chr2 | 69314780 | 69392227 |
| a0002 | 0/0 | 699 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | MCGIF others(694): Show |
chr2 | 69314780 | 69392227 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2097 | 318 | 88 | 57 | 129 | 10 | 32 | GFPT1_chr2_69314780_69392227 | GFPT1 | ATGTG others(2092): Show |
chr2 | 69314780 | 69392227 | ||
| a0001c0002 | 0/0 | 2097 | 44 | 2 | 0 | 39 | 0 | 3 | GFPT1_chr2_69314780_69392227 | GFPT1 | ATGTG others(2092): Show |
chr2 | 69314780 | 69392227 | ||
| a0001c0003 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | ATGTG others(2092): Show |
chr2 | 69314780 | 69392227 | ||
| a0001c0005 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | ATGTG others(2092): Show |
chr2 | 69314780 | 69392227 | ||
| a0001c0006 | 0/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | ATGTG others(2092): Show |
chr2 | 69314780 | 69392227 | ||
| a0002c0004 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | ATGTG others(2092): Show |
chr2 | 69314780 | 69392227 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 8665 | 95 | 4 | 23 | 58 | 1 | 8 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0002 | 0/0 | 8664 | 88 | 30 | 16 | 32 | 2 | 8 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0003 | 0/1 | 8664 | 37 | 14 | 7 | 6 | 4 | 5 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0005 | 0/0 | 8665 | 19 | 2 | 0 | 14 | 0 | 3 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0007 | 0/0 | 8664 | 7 | 7 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0008 | 0/0 | 8664 | 6 | 1 | 3 | 0 | 1 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0009 | 0/0 | 8664 | 5 | 5 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0010 | 0/0 | 8664 | 5 | 0 | 0 | 5 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0011 | 0/0 | 8665 | 4 | 4 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0012 | 0/0 | 8665 | 4 | 0 | 2 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0013 | 0/0 | 8665 | 3 | 3 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0014 | 0/0 | 8663 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8658): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0015 | 0/0 | 8664 | 3 | 2 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0016 | 0/0 | 8665 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0018 | 0/0 | 8663 | 2 | 0 | 1 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8658): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0019 | 0/0 | 8667 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8662): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0020 | 0/0 | 8666 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8661): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0021 | 0/0 | 8664 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0022 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAAG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0023 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0024 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0025 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0026 | 0/0 | 8742 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8737): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0027 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0028 | 0/0 | 8665 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0029 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0030 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0031 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0032 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0033 | 0/0 | 8665 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0034 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0035 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0036 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0037 | 0/0 | 8663 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8658): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0038 | 0/0 | 8663 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8658): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0041 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0042 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0043 | 0/0 | 8664 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0044 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0045 | 0/0 | 8664 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0047 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0048 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0049 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0050 | 0/0 | 8663 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8658): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0052 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0055 | 0/0 | 8665 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0001t0056 | 0/0 | 8665 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0002t0004 | 0/0 | 8661 | 22 | 2 | 0 | 18 | 0 | 2 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8656): Show |
chr2 | 69314780 | 69392227 |
| a0001c0002t0006 | 0/0 | 8661 | 14 | 0 | 0 | 14 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8656): Show |
chr2 | 69314780 | 69392227 |
| a0001c0002t0017 | 0/0 | 8661 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8656): Show |
chr2 | 69314780 | 69392227 |
| a0001c0002t0039 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8655): Show |
chr2 | 69314780 | 69392227 |
| a0001c0002t0040 | 0/0 | 8662 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8657): Show |
chr2 | 69314780 | 69392227 |
| a0001c0002t0046 | 0/0 | 8661 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8656): Show |
chr2 | 69314780 | 69392227 |
| a0001c0002t0051 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8655): Show |
chr2 | 69314780 | 69392227 |
| a0001c0002t0053 | 0/0 | 8661 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8656): Show |
chr2 | 69314780 | 69392227 |
| a0001c0002t0054 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8655): Show |
chr2 | 69314780 | 69392227 |
| a0001c0003t0002 | 0/0 | 8664 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8659): Show |
chr2 | 69314780 | 69392227 |
| a0001c0005t0001 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0001c0006t0001 | 0/0 | 8665 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| a0002c0004t0001 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | GAAGG others(8660): Show |
chr2 | 69314780 | 69392227 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0006 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0037 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0008g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0008g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0008g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0010g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0010g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0010g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0011g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0011g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0011g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0011g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0012g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0012g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0012g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0012g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0013g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0013g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0014g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0014g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0014g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0015g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0015g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0015g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0016g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0016g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0018g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0018g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0019g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0019g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0020g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0020g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0021g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0021g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0022g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0023g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0024g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0025g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0026g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0027g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0028g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0029g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0030g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0031g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0032g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0033g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0034g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0035g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0036g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0037g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0038g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0041g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0042g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0043g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0044g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0045g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0047g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0048g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0049g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0050g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0052g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0055g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0001t0056g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0017g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0017g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0039g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0040g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0046g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0051g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0053g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0002t0054g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0003t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0005t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0001c0006t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| a0002c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0186 | EUR | GBR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00408 | hp1 | a0001 | c0001 | t0027 | g0276 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00544 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00597 | hp1 | a0001 | c0002 | t0004 | g0156 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00597 | hp2 | a0001 | c0001 | t0010 | g0202 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00609 | hp1 | a0001 | c0002 | t0006 | g0126 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00621 | hp1 | a0001 | c0002 | t0006 | g0244 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00673 | hp1 | a0001 | c0001 | t0010 | g0188 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00735 | hp2 | a0001 | c0001 | t0033 | g0248 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00738 | hp2 | a0001 | c0001 | t0008 | g0013 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01069 | hp2 | a0001 | c0003 | t0002 | g0220 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01167 | hp1 | a0001 | c0001 | t0018 | g0176 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01167 | hp2 | a0001 | c0001 | t0038 | g0243 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01243 | hp1 | a0001 | c0001 | t0015 | g0038 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01243 | hp2 | a0001 | c0001 | t0056 | g0339 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0172 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01433 | hp1 | a0001 | c0001 | t0012 | g0034 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01496 | hp1 | a0001 | c0001 | t0055 | g0262 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0221 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | IBS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01515 | hp2 | a0001 | c0001 | t0036 | g0219 | EUR | IBS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0065 | EUR | IBS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01516 | hp2 | a0001 | c0001 | t0008 | g0182 | EUR | IBS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01517 | hp1 | a0001 | c0001 | t0037 | g0183 | EUR | IBS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | IBS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0030 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01978 | hp2 | a0001 | c0001 | t0012 | g0237 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02015 | hp1 | a0001 | c0002 | t0006 | g0153 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02027 | hp1 | a0001 | c0001 | t0045 | g0190 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0101 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02083 | hp1 | a0001 | c0002 | t0004 | g0137 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02132 | hp1 | a0001 | c0002 | t0004 | g0139 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02145 | hp1 | a0001 | c0001 | t0030 | g0330 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CDX | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02257 | hp2 | a0001 | c0001 | t0020 | g0123 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02451 | hp2 | a0001 | c0001 | t0024 | g0049 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0105 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0047 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02717 | hp1 | a0001 | c0001 | t0025 | g0023 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02723 | hp1 | a0001 | c0001 | t0022 | g0020 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02735 | hp1 | a0001 | c0001 | t0050 | g0078 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02738 | hp1 | a0001 | c0002 | t0004 | g0141 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02886 | hp1 | a0001 | c0001 | t0047 | g0196 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02895 | hp2 | a0001 | c0001 | t0019 | g0124 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0045 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02897 | hp1 | a0001 | c0001 | t0019 | g0125 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02922 | hp1 | a0001 | c0001 | t0023 | g0021 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02965 | hp1 | a0001 | c0001 | t0011 | g0120 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0040 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0043 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03041 | hp2 | a0001 | c0001 | t0020 | g0122 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03098 | hp1 | a0001 | c0001 | t0021 | g0193 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03139 | hp2 | a0001 | c0001 | t0034 | g0247 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0118 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0231 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03239 | hp1 | a0001 | c0001 | t0032 | g0275 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03239 | hp2 | a0001 | c0001 | t0008 | g0203 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0046 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0086 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0075 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03540 | hp1 | a0001 | c0001 | t0021 | g0194 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03579 | hp1 | a0001 | c0001 | t0041 | g0106 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03654 | hp2 | a0001 | c0001 | t0042 | g0070 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03669 | hp2 | a0001 | c0001 | t0044 | g0052 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03710 | hp2 | a0001 | c0006 | t0001 | g0333 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03831 | hp1 | a0001 | c0001 | t0031 | g0326 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03834 | hp1 | a0001 | c0001 | t0028 | g0249 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG04184 | hp2 | a0001 | c0002 | t0004 | g0158 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0228 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG04204 | hp2 | a0001 | c0001 | t0049 | g0111 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0117 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG04228 | hp2 | a0001 | c0002 | t0046 | g0050 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | YRI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | YRI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18612 | hp2 | a0001 | c0001 | t0052 | g0099 | EAS | CHB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18906 | hp1 | a0001 | c0001 | t0015 | g0039 | AFR | YRI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | YRI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18942 | hp1 | a0001 | c0001 | t0010 | g0184 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18942 | hp2 | a0001 | c0002 | t0054 | g0151 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18943 | hp1 | a0001 | c0002 | t0006 | g0154 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18946 | hp1 | a0001 | c0001 | t0018 | g0054 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18946 | hp2 | a0001 | c0002 | t0051 | g0130 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18952 | hp1 | a0001 | c0002 | t0017 | g0140 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18952 | hp2 | a0001 | c0001 | t0014 | g0293 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18954 | hp2 | a0001 | c0002 | t0004 | g0131 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18956 | hp1 | a0001 | c0002 | t0004 | g0129 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18963 | hp1 | a0001 | c0002 | t0004 | g0128 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18964 | hp1 | a0001 | c0002 | t0004 | g0157 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18964 | hp2 | a0001 | c0001 | t0012 | g0233 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18966 | hp2 | a0002 | c0004 | t0001 | g0320 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18970 | hp1 | a0001 | c0001 | t0016 | g0307 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18972 | hp2 | a0001 | c0002 | t0006 | g0016 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18973 | hp1 | a0001 | c0002 | t0004 | g0148 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18980 | hp2 | a0001 | c0002 | t0006 | g0245 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18988 | hp2 | a0001 | c0002 | t0006 | g0132 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18992 | hp1 | a0001 | c0002 | t0006 | g0135 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19001 | hp2 | a0001 | c0002 | t0006 | g0246 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19002 | hp1 | a0001 | c0002 | t0006 | g0134 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19003 | hp2 | a0001 | c0002 | t0004 | g0155 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19005 | hp1 | a0001 | c0002 | t0004 | g0145 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19006 | hp1 | a0001 | c0001 | t0010 | g0217 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19009 | hp2 | a0001 | c0001 | t0010 | g0197 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19010 | hp1 | a0001 | c0002 | t0006 | g0136 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19011 | hp2 | a0001 | c0002 | t0004 | g0127 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | LWK | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19030 | hp2 | a0001 | c0001 | t0013 | g0051 | AFR | LWK | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19058 | hp1 | a0001 | c0001 | t0014 | g0296 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19060 | hp2 | a0001 | c0002 | t0004 | g0149 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19063 | hp1 | a0001 | c0002 | t0004 | g0142 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19065 | hp2 | a0001 | c0002 | t0017 | g0150 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19066 | hp2 | a0001 | c0002 | t0004 | g0144 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19067 | hp1 | a0001 | c0001 | t0012 | g0209 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19068 | hp1 | a0001 | c0002 | t0006 | g0159 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19070 | hp1 | a0001 | c0001 | t0029 | g0267 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19070 | hp2 | a0001 | c0002 | t0006 | g0016 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19074 | hp1 | a0001 | c0001 | t0043 | g0181 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19075 | hp1 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19075 | hp2 | a0001 | c0001 | t0014 | g0298 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19077 | hp1 | a0001 | c0005 | t0001 | g0316 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19078 | hp1 | a0001 | c0002 | t0039 | g0152 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19079 | hp1 | a0001 | c0002 | t0053 | g0138 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19080 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19081 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19084 | hp1 | a0001 | c0002 | t0040 | g0147 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19088 | hp2 | a0001 | c0002 | t0004 | g0143 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19089 | hp1 | a0001 | c0001 | t0016 | g0278 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19089 | hp2 | a0001 | c0001 | t0026 | g0168 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19090 | hp2 | a0001 | c0002 | t0006 | g0133 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | YRI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA19240 | hp2 | a0001 | c0001 | t0035 | g0107 | AFR | YRI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ASW | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA20129 | hp2 | a0001 | c0001 | t0013 | g0089 | AFR | ASW | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0074 | EUR | TSI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0191 | EUR | TSI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02109 | hp2 | a0001 | c0001 | t0013 | g0022 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0121 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0119 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | USA | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | USA | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | USA | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0146 | AFR | USA | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | LWK | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| NA21309 | hp2 | a0001 | c0001 | t0048 | g0041 | AFR | LWK | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0037 | REF | REF | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0006 | REF | REF | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69363562 | C | T | 1 | a0002 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.332G>A | p.Arg111His | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/20 | 488/8665 | 332/2100 | 111/699 | chr2 | 69363562 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69329393 | G | A | 1 | a0001c0006 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1629C>T | p.Asp543Asp | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/20 | 1785/8665 | 1629/2100 | 543/699 | chr2 | 69329393 | |||
| chr2:69354499 | G | A | 1 | a0001c0002 | 44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
synonymous_variant | LOW | c.675C>T | p.Leu225Leu | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 8/20 | 831/8665 | 675/2100 | 225/699 | chr2 | 69354499 | |||
| chr2:69356525 | A | C | 1 | a0001c0005 | 1 | NA19077.hp1 | synonymous_variant | LOW | c.576T>G | p.Val192Val | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/20 | 732/8665 | 576/2100 | 192/699 | chr2 | 69356525 | |||
| chr2:69370077 | A | G | 1 | a0001c0003 | 1 | HG01069.hp2 | synonymous_variant | LOW | c.147T>C | p.Asp49Asp | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/20 | 303/8665 | 147/2100 | 49/699 | chr2 | 69370077 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69319823 | A | G | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6366T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 6366 | chr2 | 69319823 | ||||||
| chr2:69319884 | A | G | 1 | a0001c0001t0029 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6305T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 6305 | chr2 | 69319884 | ||||||
| chr2:69320095 | G | A | 1 | a0001c0001t0007 | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6094C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 6094 | chr2 | 69320095 | ||||||
| chr2:69320104 | G | C | 44 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(41): Show |
252 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*6085C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 6085 | chr2 | 69320104 | ||||||
| chr2:69320186 | C | A | 2 | a0001c0001t0034 a0001c0001t0056 |
2 | HG01243.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6003G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 6003 | chr2 | 69320186 | ||||||
| chr2:69320409 | T | C | 1 | a0001c0002t0046 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5780A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 5780 | chr2 | 69320409 | ||||||
| chr2:69320413 | C | G | 1 | a0001c0001t0044 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5776G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 5776 | chr2 | 69320413 | ||||||
| chr2:69320516 | G | A | 1 | a0001c0001t0043 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5673C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 5673 | chr2 | 69320516 | ||||||
| chr2:69320725 | T | C | 2 | a0001c0001t0036 a0001c0001t0037 |
2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5464A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 5464 | chr2 | 69320725 | ||||||
| chr2:69320787 | C | CA | 3 | a0001c0001t0005 a0001c0001t0049 a0001c0001t0052 |
21 | HG02074.hp1 HG02451.hp1 HG02602.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5401dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 5401 | chr2 | 69320787 | ||||||
| chr2:69321188 | C | T | 45 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(42): Show |
253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*5001G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 5001 | chr2 | 69321188 | ||||||
| chr2:69321363 | T | G | 5 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0042 others(2): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4826A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4826 | chr2 | 69321363 | ||||||
| chr2:69321459 | C | T | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(38): Show |
244 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*4730G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4730 | chr2 | 69321459 | ||||||
| chr2:69321509 | A | T | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4680T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4680 | chr2 | 69321509 | ||||||
| chr2:69321574 | C | T | 1 | a0001c0001t0056 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4615G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4615 | chr2 | 69321574 | ||||||
| chr2:69321786 | C | A | 2 | a0001c0001t0013 a0001c0001t0025 |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4403G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4403 | chr2 | 69321786 | ||||||
| chr2:69321845 | ATG | A | 1 | a0001c0001t0014 | 3 | NA18952.hp2 NA19058.hp1 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4342_*4343delCA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4342 | chr2 | 69321845 | ||||||
| chr2:69321886 | T | C | 1 | a0001c0001t0045 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4303A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4303 | chr2 | 69321886 | ||||||
| chr2:69321915 | T | A | 1 | a0001c0001t0034 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4274A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4274 | chr2 | 69321915 | ||||||
| chr2:69322130 | T | C | 42 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(39): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*4059A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4059 | chr2 | 69322130 | ||||||
| chr2:69322136 | A | T | 1 | a0001c0001t0042 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4053T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4053 | chr2 | 69322136 | ||||||
| chr2:69322199 | AAAT | A | 9 | a0001c0002t0004 a0001c0002t0006 a0001c0002t0017 others(6): Show |
44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*3987_*3989delATT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3987 | chr2 | 69322199 | ||||||
| chr2:69322408 | C | A | 4 | a0001c0002t0006 a0001c0002t0039 a0001c0002t0053 others(1): Show |
17 | HG00609.hp1 HG00621.hp1 HG02015.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3781G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3781 | chr2 | 69322408 | ||||||
| chr2:69322613 | T | C | 1 | a0001c0002t0017 | 2 | NA18952.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3576A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3576 | chr2 | 69322613 | ||||||
| chr2:69322751 | T | C | 1 | a0001c0001t0032 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3438A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3438 | chr2 | 69322751 | ||||||
| chr2:69322842 | T | C | 1 | a0001c0001t0030 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3347A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3347 | chr2 | 69322842 | ||||||
| chr2:69322844 | G | A | 1 | a0001c0001t0007 | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3345C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3345 | chr2 | 69322844 | ||||||
| chr2:69322904 | T | C | 45 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(42): Show |
253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*3285A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3285 | chr2 | 69322904 | ||||||
| chr2:69322994 | T | C | 1 | a0001c0001t0047 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3195A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3195 | chr2 | 69322994 | ||||||
| chr2:69323055 | T | C | 1 | a0001c0001t0010 | 5 | HG00597.hp2 HG00673.hp1 NA18942.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3134A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3134 | chr2 | 69323055 | ||||||
| chr2:69323098 | T | G | 42 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(39): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*3091A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3091 | chr2 | 69323098 | ||||||
| chr2:69323124 | C | T | 47 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(44): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*3065G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3065 | chr2 | 69323124 | ||||||
| chr2:69323273 | T | C | 1 | a0001c0001t0033 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2916A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2916 | chr2 | 69323273 | ||||||
| chr2:69323282 | G | A | 2 | a0001c0001t0013 a0001c0001t0025 |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2907C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2907 | chr2 | 69323282 | ||||||
| chr2:69323391 | G | T | 1 | a0001c0001t0041 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2798C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2798 | chr2 | 69323391 | ||||||
| chr2:69323504 | T | C | 2 | a0001c0001t0015 a0001c0001t0048 |
4 | HG01243.hp1 HG02970.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2685A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2685 | chr2 | 69323504 | ||||||
| chr2:69323520 | G | A | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(38): Show |
244 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*2669C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2669 | chr2 | 69323520 | ||||||
| chr2:69323637 | T | C | 1 | a0001c0001t0048 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2552A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2552 | chr2 | 69323637 | ||||||
| chr2:69323678 | A | T | 2 | a0001c0001t0013 a0001c0001t0025 |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2511T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2511 | chr2 | 69323678 | ||||||
| chr2:69323678 | AT | A | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(28): Show |
229 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2510delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2510 | chr2 | 69323678 | ||||||
| chr2:69323678 | ATT | A | 8 | a0001c0001t0018 a0001c0001t0037 a0001c0001t0038 others(5): Show |
9 | HG01167.hp1 HG01167.hp2 HG01517.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2509_*2510delAA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2509 | chr2 | 69323678 | ||||||
| chr2:69323679 | T | A | 2 | a0001c0001t0001 a0001c0001t0012 |
2 | HG01433.hp1 NA18956.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2510A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2510 | chr2 | 69323679 | ||||||
| chr2:69323825 | G | A | 1 | a0001c0001t0033 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2364C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2364 | chr2 | 69323825 | ||||||
| chr2:69323879 | T | C | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(38): Show |
244 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*2310A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2310 | chr2 | 69323879 | ||||||
| chr2:69323920 | T | C | 42 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(39): Show |
245 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*2269A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2269 | chr2 | 69323920 | ||||||
| chr2:69323966 | G | A | 1 | a0001c0001t0052 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2223C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2223 | chr2 | 69323966 | ||||||
| chr2:69323970 | G | A | 2 | a0001c0001t0019 a0001c0001t0020 |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2219C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2219 | chr2 | 69323970 | ||||||
| chr2:69324201 | T | TTG | 2 | a0001c0001t0019 a0001c0001t0020 |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1986_*1987dupCA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1987 | chr2 | 69324201 | ||||||
| chr2:69324369 | C | T | 1 | a0001c0002t0039 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1820G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1820 | chr2 | 69324369 | ||||||
| chr2:69324402 | A | ACAGATCT others(71): Show |
1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1786_*1787insATAG others(74): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1786 | chr2 | 69324402 | ||||||
| chr2:69324451 | G | T | 1 | a0001c0001t0016 | 2 | NA18970.hp1 NA19089.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1738C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1738 | chr2 | 69324451 | ||||||
| chr2:69324547 | A | T | 1 | a0001c0001t0028 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1642T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1642 | chr2 | 69324547 | ||||||
| chr2:69324548 | A | G | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1641T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1641 | chr2 | 69324548 | ||||||
| chr2:69324549 | G | A | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1640C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1640 | chr2 | 69324549 | ||||||
| chr2:69324667 | G | C | 2 | a0001c0002t0053 a0001c0002t0054 |
2 | NA18942.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1522C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1522 | chr2 | 69324667 | ||||||
| chr2:69324687 | A | G | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1502T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1502 | chr2 | 69324687 | ||||||
| chr2:69324705 | G | T | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1484C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1484 | chr2 | 69324705 | ||||||
| chr2:69324837 | A | T | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1352T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1352 | chr2 | 69324837 | ||||||
| chr2:69324945 | C | A | 1 | a0001c0001t0007 | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1244G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1244 | chr2 | 69324945 | ||||||
| chr2:69324995 | G | T | 1 | a0001c0001t0027 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1194C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1194 | chr2 | 69324995 | ||||||
| chr2:69325104 | T | C | 2 | a0001c0001t0021 a0001c0001t0023 |
3 | HG02922.hp1 HG03098.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1085A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1085 | chr2 | 69325104 | ||||||
| chr2:69325136 | C | T | 1 | a0001c0001t0038 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1053G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1053 | chr2 | 69325136 | ||||||
| chr2:69325319 | G | T | 3 | a0001c0001t0008 a0001c0001t0036 a0001c0001t0037 |
8 | HG00738.hp2 HG01361.hp2 HG01496.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*870C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 870 | chr2 | 69325319 | ||||||
| chr2:69325322 | C | T | 1 | a0001c0001t0035 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*867G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 867 | chr2 | 69325322 | ||||||
| chr2:69325333 | A | G | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*856T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 856 | chr2 | 69325333 | ||||||
| chr2:69325389 | C | A | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(38): Show |
244 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*800G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 800 | chr2 | 69325389 | ||||||
| chr2:69325407 | A | C | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*782T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 782 | chr2 | 69325407 | ||||||
| chr2:69325427 | C | G | 1 | a0001c0001t0025 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*762G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 762 | chr2 | 69325427 | ||||||
| chr2:69325586 | C | T | 2 | a0001c0001t0009 a0001c0001t0024 |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*603G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 603 | chr2 | 69325586 | ||||||
| chr2:69325626 | C | A | 1 | a0001c0001t0055 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*563G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 563 | chr2 | 69325626 | ||||||
| chr2:69387186 | G | A | 1 | a0001c0001t0056 | 1 | HG01243.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-115C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/20 | chr2 | 69387186 | |||||||
| chr2:69387217 | C | T | 1 | a0001c0001t0023 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-146G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/20 | 146 | chr2 | 69387217 | ||||||
| chr2:69387224 | C | T | 1 | a0001c0001t0022 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-153G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/20 | 153 | chr2 | 69387224 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69326243 | GA | G | 186 | a0001c0001t0001g0306 a0001c0001t0002g0004 a0001c0001t0002g0011 others(183): Show |
197 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.2056-11delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326243 | |||||||
| chr2:69326243 | GAA | G | 49 | a0001c0001t0002g0033 a0001c0001t0009g0044 a0001c0001t0009g0045 others(46): Show |
52 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.2056-12_2056-11del others(2): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326243 | |||||||
| chr2:69326244 | A | G | 1 | a0001c0001t0026g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2056-11T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326244 | |||||||
| chr2:69326256 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0012g0034 |
2 | HG01433.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2056-23T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326256 | |||||||
| chr2:69326461 | A | T | 1 | a0001c0001t0026g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2056-228T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326461 | |||||||
| chr2:69326488 | A | G | 6 | a0001c0001t0010g0184 a0001c0001t0010g0188 a0001c0001t0010g0197 others(3): Show |
6 | HG00597.hp2 HG00673.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2056-255T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326488 | |||||||
| chr2:69326526 | A | C | 51 | a0001c0001t0001g0252 a0001c0001t0001g0308 a0001c0001t0001g0309 others(48): Show |
54 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2056-293T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326526 | |||||||
| chr2:69326729 | T | TC | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2055+184dupG | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326729 | |||||||
| chr2:69326800 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2055+114C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326800 | |||||||
| chr2:69327106 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1894-31T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327106 | |||||||
| chr2:69327128 | G | T | 5 | a0001c0001t0002g0042 a0001c0001t0015g0038 a0001c0001t0015g0039 others(2): Show |
5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1894-53C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327128 | |||||||
| chr2:69327175 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1894-100T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327175 | |||||||
| chr2:69327182 | C | T | 3 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0048 |
3 | HG02559.hp1 HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1894-107G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327182 | |||||||
| chr2:69327229 | C | A | 1 | a0001c0001t0002g0201 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1894-154G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327229 | |||||||
| chr2:69327238 | G | A | 3 | a0001c0001t0003g0066 a0001c0001t0003g0074 a0001c0001t0003g0075 |
3 | HG01168.hp1 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1894-163C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327238 | |||||||
| chr2:69327254 | T | C | 1 | a0001c0001t0002g0215 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1894-179A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327254 | |||||||
| chr2:69327380 | C | T | 1 | a0001c0001t0026g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1894-305G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327380 | |||||||
| chr2:69327382 | T | C | 1 | a0001c0001t0026g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1894-307A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327382 | |||||||
| chr2:69327420 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1894-345T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327420 | |||||||
| chr2:69327478 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1894-403C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327478 | |||||||
| chr2:69327519 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1894-444A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327519 | |||||||
| chr2:69327739 | G | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0053 a0001c0001t0002g0164 others(1): Show |
5 | HG02056.hp2 HG02135.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1893+532C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327739 | |||||||
| chr2:69327757 | C | G | 1 | a0001c0001t0002g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1893+514G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327757 | |||||||
| chr2:69327829 | G | T | 6 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1893+442C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327829 | |||||||
| chr2:69328094 | C | CA | 14 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0001c0001t0001g0277 others(11): Show |
14 | HG01243.hp2 HG01261.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.1893+176dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69328094 | |||||||
| chr2:69328094 | CA | C | 212 | a0001c0001t0001g0294 a0001c0001t0002g0004 a0001c0001t0002g0011 others(209): Show |
226 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(223): Show |
intron_variant | MODIFIER | c.1893+176delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69328094 | |||||||
| chr2:69328549 | G | T | 1 | a0001c0001t0001g0311 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1726-111C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328549 | |||||||
| chr2:69328700 | C | CTTT | 3 | a0001c0001t0008g0013 a0001c0001t0008g0221 a0001c0003t0002g0220 |
4 | HG00738.hp2 HG01069.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1726-263_1726-262i others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328700 | |||||||
| chr2:69328700 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1726-262G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328700 | |||||||
| chr2:69328701 | C | CT | 90 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(87): Show |
94 | HG00558.hp1 HG00642.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.1726-264dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328701 | |||||||
| chr2:69328701 | C | CTT | 11 | a0001c0001t0002g0094 a0001c0001t0003g0084 a0001c0001t0005g0109 others(8): Show |
11 | HG01516.hp2 HG02257.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1726-265_1726-264d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328701 | |||||||
| chr2:69328701 | C | CTTT | 89 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(86): Show |
95 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1726-266_1726-264d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328701 | |||||||
| chr2:69328701 | C | T | 3 | a0001c0001t0008g0013 a0001c0001t0008g0221 a0001c0003t0002g0220 |
4 | HG00738.hp2 HG01069.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1726-263G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328701 | |||||||
| chr2:69328726 | A | G | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-288T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328726 | |||||||
| chr2:69328770 | G | A | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1726-332C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328770 | |||||||
| chr2:69328843 | G | C | 1 | a0001c0001t0001g0290 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1726-405C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328843 | |||||||
| chr2:69328860 | C | A | 1 | a0001c0001t0001g0334 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1726-422G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328860 | |||||||
| chr2:69328915 | C | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725+382G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328915 | |||||||
| chr2:69329012 | A | C | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1725+285T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69329012 | |||||||
| chr2:69329113 | T | C | 1 | a0001c0001t0001g0331 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1725+184A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69329113 | |||||||
| chr2:69329169 | C | A | 41 | a0001c0002t0004g0003 a0001c0002t0004g0127 a0001c0002t0004g0128 others(38): Show |
44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1725+128G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69329169 | |||||||
| chr2:69329559 | C | T | 7 | a0001c0001t0002g0036 a0001c0001t0002g0110 a0001c0001t0002g0112 others(4): Show |
7 | HG02572.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597+125G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 16/19 | chr2 | 69329559 | |||||||
| chr2:69329569 | G | A | 1 | a0001c0001t0009g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1597+115C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 16/19 | chr2 | 69329569 | |||||||
| chr2:69329931 | G | A | 1 | a0001c0001t0008g0182 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1483-133C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69329931 | |||||||
| chr2:69330016 | G | A | 1 | a0001c0001t0013g0022 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1483-218C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330016 | |||||||
| chr2:69330018 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1483-220C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330018 | |||||||
| chr2:69330338 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1483-540A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330338 | |||||||
| chr2:69330462 | C | G | 1 | a0002c0004t0001g0320 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1483-664G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330462 | |||||||
| chr2:69330495 | A | AT | 49 | a0001c0001t0002g0033 a0001c0001t0009g0044 a0001c0001t0009g0045 others(46): Show |
52 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1483-698dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330495 | |||||||
| chr2:69330512 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1483-714G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330512 | |||||||
| chr2:69330584 | A | T | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483-786T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330584 | |||||||
| chr2:69330980 | C | T | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1483-1182G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330980 | |||||||
| chr2:69330996 | T | A | 5 | a0001c0001t0001g0256 a0001c0001t0001g0266 a0001c0001t0001g0277 others(2): Show |
5 | HG01261.hp2 HG01361.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1483-1198A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330996 | |||||||
| chr2:69331107 | G | A | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1483-1309C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331107 | |||||||
| chr2:69331141 | G | A | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1483-1343C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331141 | |||||||
| chr2:69331434 | C | T | 1 | a0001c0001t0002g0094 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1483-1636G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331434 | |||||||
| chr2:69331452 | C | T | 4 | a0001c0001t0002g0174 a0001c0001t0021g0193 a0001c0001t0021g0194 others(1): Show |
4 | HG02922.hp1 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483-1654G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331452 | |||||||
| chr2:69331456 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1483-1658G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331456 | |||||||
| chr2:69331591 | A | G | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.1483-1793T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331591 | |||||||
| chr2:69331620 | C | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1483-1822G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331620 | |||||||
| chr2:69331641 | T | C | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483-1843A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331641 | |||||||
| chr2:69331709 | A | C | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.1483-1911T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331709 | |||||||
| chr2:69331746 | TAGTA | T | 124 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(121): Show |
132 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.1483-1952_1483-194 others(8): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331746 | |||||||
| chr2:69331774 | A | T | 1 | a0001c0001t0002g0025 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1483-1976T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331774 | |||||||
| chr2:69331810 | T | C | 3 | a0001c0001t0015g0038 a0001c0001t0015g0039 a0001c0001t0048g0041 |
3 | HG01243.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1483-2012A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331810 | |||||||
| chr2:69331838 | A | G | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1483-2040T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331838 | |||||||
| chr2:69331947 | C | T | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483-2149G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331947 | |||||||
| chr2:69332078 | T | C | 1 | a0001c0002t0004g0157 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1483-2280A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332078 | |||||||
| chr2:69332088 | A | G | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483-2290T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332088 | |||||||
| chr2:69332147 | T | C | 1 | a0001c0001t0001g0310 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1483-2349A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332147 | |||||||
| chr2:69332313 | C | CT | 8 | a0001c0001t0002g0042 a0001c0001t0003g0075 a0001c0001t0015g0038 others(5): Show |
8 | HG01243.hp1 HG02970.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1483-2516dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332313 | |||||||
| chr2:69332318 | T | C | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483-2520A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332318 | |||||||
| chr2:69332458 | C | A | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1483-2660G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332458 | |||||||
| chr2:69332458 | C | T | 1 | a0001c0002t0006g0154 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1483-2660G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332458 | |||||||
| chr2:69332488 | G | A | 1 | a0001c0001t0044g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1483-2690C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332488 | |||||||
| chr2:69332507 | G | C | 1 | a0001c0001t0026g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1483-2709C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332507 | |||||||
| chr2:69332767 | G | C | 4 | a0001c0001t0015g0038 a0001c0001t0015g0039 a0001c0001t0015g0040 others(1): Show |
4 | HG01243.hp1 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483-2969C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332767 | |||||||
| chr2:69332797 | C | T | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1483-2999G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332797 | |||||||
| chr2:69332867 | G | C | 1 | a0001c0001t0026g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1483-3069C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332867 | |||||||
| chr2:69332868 | C | G | 1 | a0001c0001t0026g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1483-3070G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332868 | |||||||
| chr2:69332877 | G | GATA | 337 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(334): Show |
362 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.1483-3080_1483-307 others(7): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332877 | |||||||
| chr2:69332892 | A | G | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1483-3094T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332892 | |||||||
| chr2:69332941 | A | G | 1 | a0001c0001t0022g0020 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1483-3143T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332941 | |||||||
| chr2:69333012 | T | G | 37 | a0001c0002t0004g0003 a0001c0002t0004g0131 a0001c0002t0004g0137 others(34): Show |
40 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1483-3214A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333012 | |||||||
| chr2:69333318 | A | G | 1 | a0001c0001t0016g0278 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1483-3520T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333318 | |||||||
| chr2:69333320 | T | C | 1 | a0001c0001t0003g0071 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1483-3522A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333320 | |||||||
| chr2:69333385 | T | A | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483-3587A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333385 | |||||||
| chr2:69333474 | A | G | 1 | a0001c0001t0028g0249 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1483-3676T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333474 | |||||||
| chr2:69333742 | T | C | 49 | a0001c0001t0002g0033 a0001c0001t0009g0044 a0001c0001t0009g0045 others(46): Show |
52 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1483-3944A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333742 | |||||||
| chr2:69333806 | G | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1483-4008C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333806 | |||||||
| chr2:69333817 | A | G | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483-4019T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333817 | |||||||
| chr2:69333908 | A | T | 1 | a0001c0001t0026g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1482+3990T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333908 | |||||||
| chr2:69333909 | G | C | 1 | a0001c0001t0026g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1482+3989C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333909 | |||||||
| chr2:69333910 | C | A | 1 | a0001c0001t0026g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1482+3988G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333910 | |||||||
| chr2:69333911 | A | G | 1 | a0001c0001t0026g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1482+3987T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333911 | |||||||
| chr2:69333940 | G | A | 1 | a0001c0001t0013g0022 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1482+3958C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333940 | |||||||
| chr2:69333941 | T | A | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.1482+3957A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333941 | |||||||
| chr2:69334067 | A | T | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482+3831T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334067 | |||||||
| chr2:69334081 | G | A | 1 | a0001c0001t0030g0330 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1482+3817C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334081 | |||||||
| chr2:69334153 | T | A | 1 | a0001c0001t0002g0211 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1482+3745A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334153 | |||||||
| chr2:69334292 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1482+3606A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334292 | |||||||
| chr2:69334396 | C | A | 11 | a0001c0001t0003g0008 a0001c0001t0003g0072 a0001c0001t0003g0076 others(8): Show |
12 | HG01891.hp2 HG02145.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1482+3502G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334396 | |||||||
| chr2:69334525 | A | T | 1 | a0001c0001t0002g0171 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1482+3373T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334525 | |||||||
| chr2:69334641 | C | T | 1 | a0001c0002t0004g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1482+3257G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334641 | |||||||
| chr2:69334676 | A | T | 30 | a0001c0001t0002g0036 a0001c0001t0002g0094 a0001c0001t0002g0110 others(27): Show |
31 | HG02074.hp1 HG02451.hp1 HG02572.hp1 others(28): Show |
intron_variant | MODIFIER | c.1482+3222T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334676 | |||||||
| chr2:69334730 | A | T | 3 | a0001c0001t0008g0182 a0001c0001t0036g0219 a0001c0001t0037g0183 |
3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1482+3168T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334730 | |||||||
| chr2:69334808 | T | A | 6 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1482+3090A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334808 | |||||||
| chr2:69334836 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1482+3062C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334836 | |||||||
| chr2:69334867 | A | AT | 3 | a0001c0001t0015g0038 a0001c0001t0015g0039 a0001c0001t0048g0041 |
3 | HG01243.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1482+3030dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334867 | |||||||
| chr2:69334995 | T | C | 91 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(88): Show |
98 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1482+2903A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334995 | |||||||
| chr2:69335153 | C | T | 128 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(125): Show |
136 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1482+2745G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335153 | |||||||
| chr2:69335169 | G | A | 2 | a0001c0001t0015g0038 a0001c0001t0048g0041 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1482+2729C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335169 | |||||||
| chr2:69335186 | T | G | 2 | a0001c0001t0002g0170 a0001c0001t0002g0242 |
2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1482+2712A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335186 | |||||||
| chr2:69335405 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1482+2493C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335405 | |||||||
| chr2:69335424 | T | C | 4 | a0001c0001t0001g0250 a0001c0001t0001g0265 a0001c0001t0001g0269 others(1): Show |
4 | NA18963.hp2 NA18972.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.1482+2474A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335424 | |||||||
| chr2:69335447 | ATTTTATG others(8): Show |
A | 1 | a0001c0001t0002g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1482+2436_1482+245 others(19): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335447 | |||||||
| chr2:69335633 | A | T | 1 | a0001c0002t0006g0132 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1482+2265T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335633 | |||||||
| chr2:69335705 | T | C | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482+2193A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335705 | |||||||
| chr2:69335717 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1482+2181G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335717 | |||||||
| chr2:69335791 | C | G | 6 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1482+2107G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335791 | |||||||
| chr2:69335801 | G | A | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.1482+2097C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335801 | |||||||
| chr2:69335813 | G | A | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1482+2085C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335813 | |||||||
| chr2:69336048 | G | A | 57 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(54): Show |
60 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1482+1850C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336048 | |||||||
| chr2:69336050 | T | G | 57 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(54): Show |
60 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1482+1848A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336050 | |||||||
| chr2:69336050 | TG | T | 184 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(181): Show |
195 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(192): Show |
intron_variant | MODIFIER | c.1482+1847delC | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336050 | |||||||
| chr2:69336051 | G | T | 57 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(54): Show |
60 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1482+1847C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336051 | |||||||
| chr2:69336339 | C | CA | 168 | a0001c0001t0001g0250 a0001c0001t0001g0265 a0001c0001t0001g0280 others(165): Show |
177 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.1482+1558dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336339 | |||||||
| chr2:69336339 | C | CAA | 65 | a0001c0001t0002g0004 a0001c0001t0002g0033 a0001c0001t0002g0042 others(62): Show |
70 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1482+1557_1482+155 others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336339 | |||||||
| chr2:69336339 | C | CAAA | 6 | a0001c0001t0015g0038 a0001c0001t0015g0039 a0001c0001t0020g0123 others(3): Show |
6 | HG01243.hp1 HG02257.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1482+1556_1482+155 others(7): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336339 | |||||||
| chr2:69336353 | A | AG | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1482+1544_1482+154 others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336353 | |||||||
| chr2:69336353 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1482+1545T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336353 | |||||||
| chr2:69336387 | A | G | 13 | a0001c0001t0002g0042 a0001c0001t0007g0027 a0001c0001t0007g0028 others(10): Show |
13 | HG01243.hp1 HG01433.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1482+1511T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336387 | |||||||
| chr2:69336415 | T | C | 16 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(13): Show |
16 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1482+1483A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336415 | |||||||
| chr2:69336422 | T | C | 1 | a0001c0001t0015g0040 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1482+1476A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336422 | |||||||
| chr2:69336602 | T | G | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1482+1296A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336602 | |||||||
| chr2:69336635 | T | TA | 8 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(5): Show |
8 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482+1262dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336635 | |||||||
| chr2:69336635 | TA | T | 92 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(89): Show |
99 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1482+1262delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336635 | |||||||
| chr2:69336642 | A | G | 1 | a0001c0001t0012g0034 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1482+1256T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336642 | |||||||
| chr2:69336663 | C | T | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1482+1235G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336663 | |||||||
| chr2:69336800 | T | A | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1482+1098A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336800 | |||||||
| chr2:69336955 | A | C | 4 | a0001c0001t0011g0118 a0001c0001t0011g0119 a0001c0001t0011g0120 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482+943T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336955 | |||||||
| chr2:69337060 | A | AT | 9 | a0001c0001t0001g0250 a0001c0001t0001g0265 a0001c0001t0001g0310 others(6): Show |
9 | HG02074.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1482+837dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337060 | |||||||
| chr2:69337060 | AT | A | 184 | a0001c0001t0001g0268 a0001c0001t0001g0274 a0001c0001t0001g0290 others(181): Show |
195 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(192): Show |
intron_variant | MODIFIER | c.1482+837delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337060 | |||||||
| chr2:69337060 | ATT | A | 10 | a0001c0001t0002g0056 a0001c0001t0002g0195 a0001c0001t0007g0027 others(7): Show |
10 | HG01516.hp2 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1482+836_1482+837d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337060 | |||||||
| chr2:69337161 | T | A | 94 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(91): Show |
101 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1482+737A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337161 | |||||||
| chr2:69337163 | C | T | 2 | a0001c0001t0002g0056 a0001c0001t0012g0034 |
2 | HG01433.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1482+735G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337163 | |||||||
| chr2:69337183 | G | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1482+715C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337183 | |||||||
| chr2:69337191 | G | C | 94 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(91): Show |
101 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1482+707C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337191 | |||||||
| chr2:69337255 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1482+643C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337255 | |||||||
| chr2:69337358 | C | G | 1 | a0001c0001t0002g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1482+540G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337358 | |||||||
| chr2:69337448 | A | G | 23 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0035 others(20): Show |
25 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1482+450T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337448 | |||||||
| chr2:69338059 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG00609.hp2 | splice_region_variant&intron_variant | LOW | c.1325-4A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 14/19 | chr2 | 69338059 | |||||||
| chr2:69338213 | T | C | 91 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(88): Show |
98 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1325-158A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 14/19 | chr2 | 69338213 | |||||||
| chr2:69338221 | C | T | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1325-166G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 14/19 | chr2 | 69338221 | |||||||
| chr2:69338324 | C | G | 2 | a0001c0001t0001g0251 a0001c0001t0001g0325 |
2 | HG01069.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1324+121G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 14/19 | chr2 | 69338324 | |||||||
| chr2:69338431 | TA | T | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1324+13delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 14/19 | chr2 | 69338431 | |||||||
| chr2:69338676 | G | A | 2 | a0001c0001t0020g0122 a0001c0001t0020g0123 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1204-111C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338676 | |||||||
| chr2:69338710 | TA | T | 242 | a0001c0001t0001g0325 a0001c0001t0002g0004 a0001c0001t0002g0011 others(239): Show |
256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.1204-146delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338710 | |||||||
| chr2:69338712 | A | T | 199 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(196): Show |
212 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.1204-147T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338712 | |||||||
| chr2:69338802 | C | CTT | 26 | a0001c0001t0002g0025 a0001c0001t0002g0033 a0001c0001t0002g0094 others(23): Show |
27 | HG01168.hp1 HG01975.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1204-239_1204-238d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338802 | |||||||
| chr2:69338802 | C | CTTT | 202 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(199): Show |
215 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(212): Show |
intron_variant | MODIFIER | c.1204-240_1204-238d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338802 | |||||||
| chr2:69338802 | C | CTTTT | 13 | a0001c0001t0002g0058 a0001c0001t0002g0179 a0001c0001t0002g0201 others(10): Show |
13 | HG00558.hp1 HG00735.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1204-241_1204-238d others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338802 | |||||||
| chr2:69338832 | G | T | 1 | a0001c0001t0005g0096 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1204-267C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338832 | |||||||
| chr2:69338881 | C | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1204-316G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338881 | |||||||
| chr2:69338885 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1204-320G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338885 | |||||||
| chr2:69339125 | G | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-560C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339125 | |||||||
| chr2:69339258 | T | G | 1 | a0001c0001t0002g0186 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1204-693A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339258 | |||||||
| chr2:69339364 | GCTCA | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1204-803_1204-800d others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339364 | |||||||
| chr2:69339390 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0261 a0001c0001t0001g0315 others(1): Show |
5 | HG00408.hp1 HG02056.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.1204-825A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339390 | |||||||
| chr2:69339399 | G | A | 4 | a0001c0001t0002g0173 a0001c0001t0002g0198 a0001c0001t0002g0199 others(1): Show |
4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204-834C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339399 | |||||||
| chr2:69339493 | C | T | 1 | a0001c0001t0005g0105 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1204-928G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339493 | |||||||
| chr2:69339707 | A | G | 1 | a0001c0001t0001g0329 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1204-1142T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339707 | |||||||
| chr2:69339722 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1204-1157A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339722 | |||||||
| chr2:69339814 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1204-1249G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339814 | |||||||
| chr2:69339848 | T | C | 4 | a0001c0001t0011g0118 a0001c0001t0011g0119 a0001c0001t0011g0120 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204-1283A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339848 | |||||||
| chr2:69339965 | T | G | 1 | a0001c0001t0002g0094 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1204-1400A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339965 | |||||||
| chr2:69340139 | ACTTTT | A | 36 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(33): Show |
39 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.1204-1579_1204-157 others(9): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340139 | |||||||
| chr2:69340140 | C | CT | 9 | a0001c0001t0001g0260 a0001c0001t0001g0280 a0001c0001t0001g0281 others(6): Show |
9 | HG01978.hp1 HG02027.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1204-1576dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340140 | |||||||
| chr2:69340140 | CTTT | C | 17 | a0001c0001t0002g0057 a0001c0001t0002g0210 a0001c0001t0002g0227 others(14): Show |
17 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1204-1578_1204-157 others(7): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340140 | |||||||
| chr2:69340140 | CTTTT | C | 184 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(181): Show |
194 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.1204-1579_1204-157 others(8): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340140 | |||||||
| chr2:69340145 | T | A | 36 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(33): Show |
39 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.1204-1580A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340145 | |||||||
| chr2:69340146 | T | A | 1 | a0001c0001t0003g0066 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1204-1581A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340146 | |||||||
| chr2:69340209 | C | T | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.1204-1644G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340209 | |||||||
| chr2:69340219 | GAGGCATG others(1523): Show |
G | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+403_1204-1655 others(3): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340219 | |||||||
| chr2:69340287 | G | A | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204-1722C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340287 | |||||||
| chr2:69340329 | G | A | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(324): Show |
350 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(347): Show |
intron_variant | MODIFIER | c.1204-1764C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340329 | |||||||
| chr2:69340544 | G | T | 240 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(237): Show |
254 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(251): Show |
intron_variant | MODIFIER | c.1203+1608C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340544 | |||||||
| chr2:69340645 | T | TA | 8 | a0001c0001t0002g0110 a0001c0001t0007g0027 a0001c0001t0007g0028 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1203+1506dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340645 | |||||||
| chr2:69340788 | C | T | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1203+1364G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340788 | |||||||
| chr2:69340852 | G | A | 237 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(234): Show |
251 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.1203+1300C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340852 | |||||||
| chr2:69340897 | C | T | 13 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0053 others(10): Show |
15 | HG02056.hp2 HG02135.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.1203+1255G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340897 | |||||||
| chr2:69340981 | A | G | 1 | a0001c0001t0025g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1203+1171T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340981 | |||||||
| chr2:69341006 | T | A | 1 | a0001c0001t0002g0178 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1203+1146A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341006 | |||||||
| chr2:69341018 | G | A | 42 | a0001c0001t0026g0168 a0001c0002t0004g0003 a0001c0002t0004g0127 others(39): Show |
45 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1203+1134C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341018 | |||||||
| chr2:69341051 | T | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203+1101A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341051 | |||||||
| chr2:69341067 | TCCTGCCT others(22): Show |
T | 1 | a0001c0001t0034g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1203+1056_1203+108 others(33): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341067 | |||||||
| chr2:69341117 | C | A | 1 | a0001c0001t0001g0281 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1203+1035G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341117 | |||||||
| chr2:69341125 | A | AT | 7 | a0001c0001t0002g0042 a0001c0001t0015g0038 a0001c0001t0015g0039 others(4): Show |
7 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.1203+1026dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341125 | |||||||
| chr2:69341125 | AT | A | 6 | a0001c0001t0001g0250 a0001c0001t0001g0265 a0001c0001t0001g0269 others(3): Show |
6 | NA18956.hp1 NA18963.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203+1026delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341125 | |||||||
| chr2:69341339 | G | A | 1 | a0001c0002t0004g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1203+813C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341339 | |||||||
| chr2:69341532 | T | C | 3 | a0001c0001t0015g0038 a0001c0001t0015g0039 a0001c0001t0048g0041 |
3 | HG01243.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1203+620A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341532 | |||||||
| chr2:69341550 | A | G | 233 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(230): Show |
247 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.1203+602T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341550 | |||||||
| chr2:69341628 | C | T | 2 | a0001c0001t0034g0247 a0001c0001t0056g0339 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1203+524G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341628 | |||||||
| chr2:69341642 | T | C | 3 | a0001c0001t0001g0268 a0001c0001t0001g0273 a0001c0001t0001g0300 |
3 | HG00741.hp1 HG02717.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1203+510A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341642 | |||||||
| chr2:69341648 | TAC | T | 52 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(49): Show |
55 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.1203+502_1203+503d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341648 | |||||||
| chr2:69341705 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1203+447A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341705 | |||||||
| chr2:69341751 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+401G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341751 | |||||||
| chr2:69341753 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+399G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341753 | |||||||
| chr2:69341754 | A | T | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+398T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341754 | |||||||
| chr2:69341755 | A | C | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+397T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341755 | |||||||
| chr2:69341759 | A | G | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+393T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341759 | |||||||
| chr2:69341760 | A | T | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+392T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341760 | |||||||
| chr2:69341762 | A | G | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+390T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341762 | |||||||
| chr2:69341955 | C | G | 1 | a0001c0001t0003g0069 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1203+197G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341955 | |||||||
| chr2:69342094 | C | T | 1 | a0001c0001t0007g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1203+58G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69342094 | |||||||
| chr2:69342316 | G | T | 5 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0103 others(2): Show |
5 | NA18961.hp2 NA18966.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1106-67C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69342316 | |||||||
| chr2:69342409 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1106-160A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69342409 | |||||||
| chr2:69342710 | T | C | 6 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1106-461A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69342710 | |||||||
| chr2:69342798 | C | T | 182 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(179): Show |
193 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.1106-549G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69342798 | |||||||
| chr2:69342975 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1106-726C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69342975 | |||||||
| chr2:69343123 | T | C | 1 | a0001c0001t0002g0161 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1106-874A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343123 | |||||||
| chr2:69343225 | G | A | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1106-976C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343225 | |||||||
| chr2:69343229 | A | C | 1 | a0001c0001t0034g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1106-980T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343229 | |||||||
| chr2:69343313 | TGAG | T | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106-1067_1106-106 others(7): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343313 | |||||||
| chr2:69343368 | C | A | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1106-1119G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343368 | |||||||
| chr2:69343414 | C | CT | 6 | a0001c0001t0002g0191 a0001c0001t0002g0206 a0001c0001t0013g0022 others(3): Show |
6 | HG00741.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1106-1166dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343414 | |||||||
| chr2:69343414 | CT | C | 23 | a0001c0001t0002g0094 a0001c0001t0002g0166 a0001c0001t0002g0167 others(20): Show |
24 | HG02074.hp1 HG02602.hp2 HG03540.hp2 others(21): Show |
intron_variant | MODIFIER | c.1106-1166delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343414 | |||||||
| chr2:69343433 | C | CA | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1106-1185dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343433 | |||||||
| chr2:69343588 | A | G | 3 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 |
3 | NA18956.hp1 NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1106-1339T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343588 | |||||||
| chr2:69343598 | G | A | 1 | a0001c0002t0046g0050 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1106-1349C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343598 | |||||||
| chr2:69343654 | C | T | 182 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(179): Show |
193 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.1106-1405G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343654 | |||||||
| chr2:69343703 | C | T | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1106-1454G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343703 | |||||||
| chr2:69343992 | T | C | 239 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(236): Show |
253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.1106-1743A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343992 | |||||||
| chr2:69344186 | C | CA | 17 | a0001c0001t0001g0258 a0001c0001t0001g0265 a0001c0001t0001g0269 others(14): Show |
17 | HG00735.hp2 HG01175.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1105+1717dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344186 | |||||||
| chr2:69344186 | C | CAA | 5 | a0001c0001t0001g0018 a0001c0001t0001g0261 a0001c0001t0001g0315 others(2): Show |
6 | HG00408.hp1 HG02056.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105+1716_1105+171 others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344186 | |||||||
| chr2:69344186 | CA | C | 54 | a0001c0001t0001g0270 a0001c0001t0002g0166 a0001c0001t0002g0173 others(51): Show |
57 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.1105+1717delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344186 | |||||||
| chr2:69344186 | CAA | C | 173 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(170): Show |
184 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1105+1716_1105+171 others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344186 | |||||||
| chr2:69344293 | C | T | 4 | a0001c0001t0011g0118 a0001c0001t0011g0119 a0001c0001t0011g0120 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105+1611G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344293 | |||||||
| chr2:69344544 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1105+1360A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344544 | |||||||
| chr2:69344565 | T | C | 1 | a0001c0001t0002g0167 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1105+1339A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344565 | |||||||
| chr2:69344591 | T | C | 41 | a0001c0002t0004g0003 a0001c0002t0004g0127 a0001c0002t0004g0128 others(38): Show |
44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1105+1313A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344591 | |||||||
| chr2:69344656 | A | AT | 77 | a0001c0001t0001g0329 a0001c0001t0003g0007 a0001c0001t0003g0008 others(74): Show |
83 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1105+1247dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344656 | |||||||
| chr2:69344662 | T | A | 1 | a0001c0001t0012g0034 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1105+1242A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344662 | |||||||
| chr2:69344663 | T | A | 8 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0264 others(5): Show |
8 | HG02071.hp1 HG02083.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1105+1241A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344663 | |||||||
| chr2:69344685 | C | T | 5 | a0001c0001t0001g0256 a0001c0001t0001g0266 a0001c0001t0001g0277 others(2): Show |
5 | HG01261.hp2 HG01361.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1105+1219G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344685 | |||||||
| chr2:69344700 | G | A | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1105+1204C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344700 | |||||||
| chr2:69344728 | C | T | 129 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(126): Show |
137 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1105+1176G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344728 | |||||||
| chr2:69344755 | C | G | 1 | a0001c0001t0005g0098 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1105+1149G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344755 | |||||||
| chr2:69344804 | C | T | 2 | a0001c0001t0034g0247 a0001c0001t0056g0339 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1105+1100G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344804 | |||||||
| chr2:69344816 | T | A | 3 | a0001c0001t0002g0236 a0001c0001t0003g0068 a0001c0001t0003g0073 |
3 | HG02630.hp1 HG02818.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1105+1088A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344816 | |||||||
| chr2:69344819 | A | G | 1 | a0001c0001t0028g0249 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1105+1085T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344819 | |||||||
| chr2:69344952 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1105+952C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344952 | |||||||
| chr2:69345159 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1105+745C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69345159 | |||||||
| chr2:69345697 | C | G | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105+207G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69345697 | |||||||
| chr2:69345788 | G | A | 1 | a0001c0002t0004g0148 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1105+116C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69345788 | |||||||
| chr2:69345897 | T | C | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
splice_region_variant&intron_variant | LOW | c.1105+7A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69345897 | |||||||
| chr2:69346141 | T | C | 235 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(232): Show |
249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.1010-142A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346141 | |||||||
| chr2:69346222 | TACA | T | 41 | a0001c0002t0004g0003 a0001c0002t0004g0127 a0001c0002t0004g0128 others(38): Show |
44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1010-226_1010-224d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346222 | |||||||
| chr2:69346387 | T | A | 3 | a0001c0001t0001g0281 a0001c0001t0001g0323 a0001c0005t0001g0316 |
3 | HG02027.hp2 NA18983.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1010-388A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346387 | |||||||
| chr2:69346396 | G | A | 1 | a0001c0002t0004g0139 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1010-397C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346396 | |||||||
| chr2:69346459 | C | T | 2 | a0001c0001t0003g0035 a0001c0001t0003g0086 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1010-460G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346459 | |||||||
| chr2:69346490 | G | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1010-491C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346490 | |||||||
| chr2:69346491 | G | T | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1010-492C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346491 | |||||||
| chr2:69346693 | C | CAT | 5 | a0001c0001t0002g0042 a0001c0001t0015g0038 a0001c0001t0015g0039 others(2): Show |
5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1010-696_1010-695d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346693 | |||||||
| chr2:69346705 | T | G | 1 | a0001c0001t0001g0288 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1010-706A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346705 | |||||||
| chr2:69346891 | G | A | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1010-892C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346891 | |||||||
| chr2:69346898 | A | T | 1 | a0001c0001t0008g0182 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1010-899T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346898 | |||||||
| chr2:69346898 | AGTTTTGT others(3): Show |
A | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1010-909_1010-900d others(12): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346898 | |||||||
| chr2:69346967 | C | T | 1 | a0001c0001t0034g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1010-968G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346967 | |||||||
| chr2:69347060 | C | T | 6 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1010-1061G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347060 | |||||||
| chr2:69347210 | CT | C | 14 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1009+960delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347210 | |||||||
| chr2:69347448 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1009+723G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347448 | |||||||
| chr2:69347480 | C | CT | 186 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(183): Show |
197 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.1009+690dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347480 | |||||||
| chr2:69347526 | G | A | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1009+645C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347526 | |||||||
| chr2:69347622 | C | T | 182 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(179): Show |
193 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.1009+549G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347622 | |||||||
| chr2:69347680 | G | A | 1 | a0001c0001t0005g0098 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1009+491C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347680 | |||||||
| chr2:69347735 | G | A | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009+436C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347735 | |||||||
| chr2:69347936 | TTAA | T | 6 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1009+232_1009+234d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347936 | |||||||
| chr2:69347971 | CATTA | C | 3 | a0001c0001t0003g0066 a0001c0001t0003g0074 a0001c0001t0003g0075 |
3 | HG01168.hp1 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1009+196_1009+199d others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347971 | |||||||
| chr2:69348041 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1009+130C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69348041 | |||||||
| chr2:69348481 | C | A | 1 | a0001c0001t0002g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.846-147G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69348481 | |||||||
| chr2:69348691 | G | C | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.846-357C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69348691 | |||||||
| chr2:69348842 | T | C | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.846-508A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69348842 | |||||||
| chr2:69348900 | G | A | 3 | a0001c0001t0011g0119 a0001c0001t0011g0120 a0001c0001t0011g0121 |
3 | HG02486.hp2 HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.846-566C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69348900 | |||||||
| chr2:69348930 | C | A | 2 | a0001c0001t0003g0080 a0001c0001t0003g0085 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.846-596G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69348930 | |||||||
| chr2:69349012 | C | T | 48 | a0001c0001t0002g0033 a0001c0001t0009g0044 a0001c0001t0009g0045 others(45): Show |
51 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.846-678G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69349012 | |||||||
| chr2:69349015 | G | C | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.846-681C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69349015 | |||||||
| chr2:69349054 | T | A | 1 | a0001c0001t0001g0272 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.846-720A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69349054 | |||||||
| chr2:69349157 | T | A | 1 | a0001c0001t0052g0099 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.846-823A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69349157 | |||||||
| chr2:69349403 | T | C | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.845+675A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69349403 | |||||||
| chr2:69349709 | G | A | 1 | a0001c0001t0015g0039 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.845+369C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69349709 | |||||||
| chr2:69350318 | G | A | 1 | a0001c0001t0011g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.740-135C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350318 | |||||||
| chr2:69350435 | A | T | 5 | a0001c0001t0002g0042 a0001c0001t0015g0038 a0001c0001t0015g0039 others(2): Show |
5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.740-252T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350435 | |||||||
| chr2:69350463 | C | T | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.740-280G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350463 | |||||||
| chr2:69350579 | C | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-396G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350579 | |||||||
| chr2:69350612 | C | T | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.740-429G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350612 | |||||||
| chr2:69350763 | C | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-580G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350763 | |||||||
| chr2:69350852 | G | A | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.740-669C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350852 | |||||||
| chr2:69350861 | C | T | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.740-678G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350861 | |||||||
| chr2:69350916 | A | G | 3 | a0001c0001t0008g0182 a0001c0001t0036g0219 a0001c0001t0037g0183 |
3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.740-733T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350916 | |||||||
| chr2:69350918 | A | G | 4 | a0001c0001t0011g0118 a0001c0001t0011g0119 a0001c0001t0011g0120 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-735T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350918 | |||||||
| chr2:69351078 | G | T | 9 | a0001c0001t0002g0094 a0001c0001t0005g0010 a0001c0001t0005g0092 others(6): Show |
10 | NA18961.hp2 NA18965.hp1 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.740-895C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351078 | |||||||
| chr2:69351159 | C | T | 13 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0053 others(10): Show |
15 | HG02056.hp2 HG02135.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.740-976G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351159 | |||||||
| chr2:69351160 | T | G | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.740-977A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351160 | |||||||
| chr2:69351333 | C | A | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.740-1150G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351333 | |||||||
| chr2:69351524 | G | A | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.740-1341C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351524 | |||||||
| chr2:69351537 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.740-1354G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351537 | |||||||
| chr2:69351791 | A | T | 1 | a0001c0001t0030g0330 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.740-1608T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351791 | |||||||
| chr2:69352008 | T | A | 1 | a0001c0001t0001g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.740-1825A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352008 | |||||||
| chr2:69352031 | G | A | 1 | a0001c0001t0001g0279 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.740-1848C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352031 | |||||||
| chr2:69352068 | C | T | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.740-1885G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352068 | |||||||
| chr2:69352318 | T | A | 238 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(235): Show |
252 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.739+1941A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352318 | |||||||
| chr2:69352332 | C | T | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.739+1927G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352332 | |||||||
| chr2:69352431 | C | T | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.739+1828G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352431 | |||||||
| chr2:69352471 | G | C | 4 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.739+1788C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352471 | |||||||
| chr2:69352483 | C | T | 2 | a0001c0001t0016g0278 a0001c0001t0016g0307 |
2 | NA18970.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.739+1776G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352483 | |||||||
| chr2:69352523 | C | G | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.739+1736G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352523 | |||||||
| chr2:69352562 | G | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+1697C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352562 | |||||||
| chr2:69352604 | C | T | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.739+1655G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352604 | |||||||
| chr2:69352612 | C | CA | 116 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0254 others(113): Show |
126 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.739+1646dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | |||||||
| chr2:69352612 | C | CAA | 106 | a0001c0001t0001g0304 a0001c0001t0002g0004 a0001c0001t0002g0033 others(103): Show |
111 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.739+1645_739+1646d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | |||||||
| chr2:69352612 | C | CAAA | 34 | a0001c0001t0002g0206 a0001c0001t0002g0234 a0001c0001t0002g0239 others(31): Show |
37 | HG00544.hp2 HG00621.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.739+1644_739+1646d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | |||||||
| chr2:69352612 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0013g0022 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.739+1634_739+1646d others(15): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | |||||||
| chr2:69352612 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0013g0051 a0001c0001t0025g0023 |
2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.739+1633_739+1646d others(16): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | |||||||
| chr2:69352612 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0013g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.739+1629_739+1646d others(20): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | |||||||
| chr2:69352612 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.739+1634_739+1646d others(15): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | |||||||
| chr2:69352777 | G | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.739+1482C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352777 | |||||||
| chr2:69352795 | C | G | 1 | a0001c0001t0001g0251 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.739+1464G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352795 | |||||||
| chr2:69352812 | G | A | 3 | a0001c0001t0003g0066 a0001c0001t0003g0074 a0001c0001t0003g0075 |
3 | HG01168.hp1 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.739+1447C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352812 | |||||||
| chr2:69352837 | G | A | 1 | a0001c0001t0005g0109 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.739+1422C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352837 | |||||||
| chr2:69352891 | C | T | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.739+1368G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352891 | |||||||
| chr2:69352947 | G | A | 2 | a0001c0001t0005g0103 a0001c0001t0005g0104 |
2 | NA18984.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.739+1312C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352947 | |||||||
| chr2:69353012 | C | T | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.739+1247G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353012 | |||||||
| chr2:69353041 | T | C | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.739+1218A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353041 | |||||||
| chr2:69353218 | A | C | 6 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.739+1041T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353218 | |||||||
| chr2:69353239 | T | A | 1 | a0001c0001t0001g0302 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.739+1020A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353239 | |||||||
| chr2:69353266 | G | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.739+993C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353266 | |||||||
| chr2:69353301 | T | C | 3 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 |
3 | NA18956.hp1 NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.739+958A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353301 | |||||||
| chr2:69353329 | G | T | 49 | a0001c0001t0002g0033 a0001c0001t0009g0044 a0001c0001t0009g0045 others(46): Show |
52 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.739+930C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353329 | |||||||
| chr2:69353354 | T | C | 1 | a0001c0001t0002g0113 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.739+905A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353354 | |||||||
| chr2:69353528 | T | A | 1 | a0001c0001t0041g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.739+731A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353528 | |||||||
| chr2:69353554 | A | G | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.739+705T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353554 | |||||||
| chr2:69353570 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.739+689C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353570 | |||||||
| chr2:69353605 | A | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.739+654T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353605 | |||||||
| chr2:69353805 | T | G | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+454A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353805 | |||||||
| chr2:69353820 | T | A | 1 | a0001c0001t0043g0181 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.739+439A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353820 | |||||||
| chr2:69353838 | C | T | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.739+421G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353838 | |||||||
| chr2:69353943 | C | T | 41 | a0001c0002t0004g0003 a0001c0002t0004g0127 a0001c0002t0004g0128 others(38): Show |
44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.739+316G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353943 | |||||||
| chr2:69354067 | C | A | 1 | a0001c0001t0003g0076 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.739+192G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69354067 | |||||||
| chr2:69354346 | T | C | 1 | a0001c0002t0004g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.686-34A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 8/19 | chr2 | 69354346 | |||||||
| chr2:69354387 | G | A | 1 | a0001c0001t0049g0111 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.686-75C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 8/19 | chr2 | 69354387 | |||||||
| chr2:69354628 | T | A | 5 | a0001c0001t0005g0096 a0001c0001t0005g0097 a0001c0001t0005g0098 others(2): Show |
5 | NA18612.hp2 NA18939.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.606-60A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354628 | |||||||
| chr2:69354718 | T | TA | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.606-151dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354718 | |||||||
| chr2:69354758 | C | A | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.606-190G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354758 | |||||||
| chr2:69354792 | A | C | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.606-224T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354792 | |||||||
| chr2:69354845 | C | T | 4 | a0001c0002t0006g0159 a0001c0002t0039g0152 a0001c0002t0053g0138 others(1): Show |
4 | NA18942.hp2 NA19068.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.606-277G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354845 | |||||||
| chr2:69354875 | G | A | 1 | a0001c0001t0002g0191 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.606-307C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354875 | |||||||
| chr2:69354896 | C | T | 129 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(126): Show |
137 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.606-328G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354896 | |||||||
| chr2:69354999 | ATATCCAA others(9): Show |
A | 5 | a0001c0001t0002g0042 a0001c0001t0015g0038 a0001c0001t0015g0039 others(2): Show |
5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.606-447_606-432del others(16): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354999 | |||||||
| chr2:69355009 | T | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.606-441A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355009 | |||||||
| chr2:69355082 | ATTTG | A | 3 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0001c0001t0007g0043 |
3 | HG02258.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.606-518_606-515del others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355082 | |||||||
| chr2:69355136 | G | C | 1 | a0001c0001t0003g0076 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.606-568C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355136 | |||||||
| chr2:69355391 | T | TG | 185 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(182): Show |
196 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.606-824dupC | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355391 | |||||||
| chr2:69355394 | T | G | 54 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(51): Show |
57 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.606-826A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355394 | |||||||
| chr2:69355408 | T | TTTC | 238 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(235): Show |
252 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.606-841_606-840ins others(3): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355408 | |||||||
| chr2:69355436 | A | G | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.606-868T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355436 | |||||||
| chr2:69355460 | T | C | 1 | a0001c0001t0008g0221 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.606-892A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355460 | |||||||
| chr2:69355575 | G | A | 3 | a0001c0001t0002g0179 a0001c0001t0002g0201 a0001c0001t0003g0077 |
3 | HG03516.hp1 HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.605+921C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355575 | |||||||
| chr2:69355680 | C | T | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.605+816G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355680 | |||||||
| chr2:69355763 | C | T | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.605+733G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355763 | |||||||
| chr2:69355817 | T | A | 1 | a0001c0001t0031g0326 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.605+679A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355817 | |||||||
| chr2:69355870 | A | G | 5 | a0001c0001t0002g0042 a0001c0001t0015g0038 a0001c0001t0015g0039 others(2): Show |
5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.605+626T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355870 | |||||||
| chr2:69355932 | T | C | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.605+564A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355932 | |||||||
| chr2:69355983 | C | CT | 9 | a0001c0001t0001g0250 a0001c0001t0001g0260 a0001c0001t0001g0264 others(6): Show |
9 | HG01496.hp1 HG01928.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.605+512dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355983 | |||||||
| chr2:69355983 | CT | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(27): Show |
35 | HG00408.hp1 HG00642.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.605+512delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355983 | |||||||
| chr2:69355983 | CTT | C | 92 | a0001c0001t0002g0015 a0001c0001t0002g0036 a0001c0001t0002g0094 others(89): Show |
97 | HG00558.hp1 HG00642.hp2 HG00741.hp2 others(94): Show |
intron_variant | MODIFIER | c.605+511_605+512del others(2): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355983 | |||||||
| chr2:69355983 | CTTT | C | 126 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(123): Show |
134 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.605+510_605+512del others(3): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355983 | |||||||
| chr2:69355983 | CTTTT | C | 11 | a0001c0001t0002g0014 a0001c0001t0002g0033 a0001c0001t0002g0163 others(8): Show |
12 | HG01167.hp1 HG01168.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.605+509_605+512del others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355983 | |||||||
| chr2:69356152 | C | G | 1 | a0001c0001t0001g0332 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.605+344G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69356152 | |||||||
| chr2:69356166 | C | G | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.605+330G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69356166 | |||||||
| chr2:69356238 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.605+258G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69356238 | |||||||
| chr2:69356269 | C | G | 1 | a0001c0001t0003g0067 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.605+227G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69356269 | |||||||
| chr2:69356290 | G | A | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.605+206C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69356290 | |||||||
| chr2:69356740 | C | T | 47 | a0001c0001t0002g0033 a0001c0001t0009g0044 a0001c0001t0009g0045 others(44): Show |
50 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.544-183G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69356740 | |||||||
| chr2:69356741 | AT | A | 230 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(227): Show |
244 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.544-185delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69356741 | |||||||
| chr2:69356743 | T | A | 1 | a0001c0002t0004g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.544-186A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69356743 | |||||||
| chr2:69356764 | A | G | 182 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(179): Show |
193 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.544-207T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69356764 | |||||||
| chr2:69357094 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.544-537A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357094 | |||||||
| chr2:69357263 | AG | A | 133 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(130): Show |
141 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.544-707delC | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357263 | |||||||
| chr2:69357347 | C | G | 2 | a0001c0001t0001g0279 a0001c0001t0001g0331 |
2 | NA18961.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.544-790G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357347 | |||||||
| chr2:69357413 | G | A | 6 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-856C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357413 | |||||||
| chr2:69357467 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.543+862T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357467 | |||||||
| chr2:69357484 | C | A | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.543+845G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357484 | |||||||
| chr2:69357553 | G | C | 1 | a0001c0001t0001g0285 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.543+776C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357553 | |||||||
| chr2:69357612 | G | A | 4 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+717C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357612 | |||||||
| chr2:69357691 | G | C | 1 | a0001c0002t0004g0139 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.543+638C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357691 | |||||||
| chr2:69357790 | C | T | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+539G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357790 | |||||||
| chr2:69358004 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.543+325G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358004 | |||||||
| chr2:69358044 | A | G | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.543+285T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358044 | |||||||
| chr2:69358136 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.543+193C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358136 | |||||||
| chr2:69358146 | T | A | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.543+183A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358146 | |||||||
| chr2:69358154 | G | C | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+175C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358154 | |||||||
| chr2:69358162 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.543+167T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358162 | |||||||
| chr2:69358224 | C | G | 1 | a0001c0001t0012g0233 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.543+105G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358224 | |||||||
| chr2:69358246 | G | C | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.543+83C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358246 | |||||||
| chr2:69358778 | C | A | 9 | a0001c0001t0002g0015 a0001c0001t0002g0173 a0001c0001t0002g0175 others(6): Show |
10 | HG01109.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.409-315G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69358778 | |||||||
| chr2:69358909 | C | T | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+359G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69358909 | |||||||
| chr2:69359137 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.408+131G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69359137 | |||||||
| chr2:69359161 | A | C | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.408+107T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69359161 | |||||||
| chr2:69359171 | C | T | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+97G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69359171 | |||||||
| chr2:69359238 | A | G | 68 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(65): Show |
73 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.408+30T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69359238 | |||||||
| chr2:69359261 | T | A | 6 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.408+7A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69359261 | |||||||
| chr2:69359432 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.350-106G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69359432 | |||||||
| chr2:69359447 | G | A | 1 | a0001c0001t0001g0321 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.350-121C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69359447 | |||||||
| chr2:69359656 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.350-330C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69359656 | |||||||
| chr2:69359756 | A | C | 1 | a0001c0001t0043g0181 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.350-430T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69359756 | |||||||
| chr2:69360156 | T | A | 1 | a0001c0001t0002g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.350-830A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360156 | |||||||
| chr2:69360224 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.350-898C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360224 | |||||||
| chr2:69360243 | C | T | 1 | a0001c0001t0002g0180 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.350-917G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360243 | |||||||
| chr2:69360328 | C | CA | 82 | a0001c0001t0001g0254 a0001c0001t0001g0257 a0001c0001t0001g0286 others(79): Show |
87 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.350-1003dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360328 | |||||||
| chr2:69360328 | C | CAA | 18 | a0001c0001t0001g0277 a0001c0001t0002g0232 a0001c0001t0002g0238 others(15): Show |
18 | HG00609.hp1 HG02148.hp1 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.350-1004_350-1003d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360328 | |||||||
| chr2:69360328 | CAAAAAAA others(2): Show |
C | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.350-1011_350-1003d others(11): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360328 | |||||||
| chr2:69360440 | A | ATT | 8 | a0001c0001t0005g0091 a0001c0001t0005g0096 a0001c0001t0009g0044 others(5): Show |
8 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-1115_350-1114i others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360440 | |||||||
| chr2:69360442 | A | AT | 88 | a0001c0001t0002g0033 a0001c0001t0002g0042 a0001c0001t0002g0208 others(85): Show |
94 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.350-1117dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360442 | |||||||
| chr2:69360442 | A | ATT | 125 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(122): Show |
133 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.350-1118_350-1117d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360442 | |||||||
| chr2:69360442 | A | ATTT | 9 | a0001c0001t0002g0206 a0001c0001t0007g0027 a0001c0001t0007g0028 others(6): Show |
9 | HG00741.hp2 HG01433.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-1119_350-1117d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360442 | |||||||
| chr2:69360442 | A | T | 11 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(8): Show |
11 | HG01109.hp2 HG01928.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.350-1116T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360442 | |||||||
| chr2:69360444 | T | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-1118A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360444 | |||||||
| chr2:69360573 | G | A | 1 | a0001c0001t0034g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.350-1247C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360573 | |||||||
| chr2:69360746 | C | G | 2 | a0001c0001t0019g0124 a0001c0001t0019g0125 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.350-1420G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360746 | |||||||
| chr2:69360923 | C | T | 91 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(88): Show |
98 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.350-1597G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360923 | |||||||
| chr2:69360963 | A | G | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.350-1637T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360963 | |||||||
| chr2:69361031 | G | A | 1 | a0001c0001t0011g0118 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.350-1705C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361031 | |||||||
| chr2:69361309 | G | A | 2 | a0001c0001t0005g0103 a0001c0001t0005g0104 |
2 | NA18984.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.350-1983C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361309 | |||||||
| chr2:69361447 | C | CA | 7 | a0001c0001t0001g0297 a0001c0001t0001g0331 a0001c0001t0002g0216 others(4): Show |
7 | HG02559.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+2097dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361447 | |||||||
| chr2:69361447 | CA | C | 222 | a0001c0001t0001g0256 a0001c0001t0001g0263 a0001c0001t0001g0279 others(219): Show |
236 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(233): Show |
intron_variant | MODIFIER | c.349+2097delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361447 | |||||||
| chr2:69361447 | CAA | C | 10 | a0001c0001t0002g0094 a0001c0001t0002g0112 a0001c0001t0002g0213 others(7): Show |
10 | HG01168.hp1 HG01516.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.349+2096_349+2097d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361447 | |||||||
| chr2:69361519 | C | T | 15 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.349+2026G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361519 | |||||||
| chr2:69361562 | G | A | 2 | a0001c0001t0003g0079 a0001c0001t0003g0082 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.349+1983C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361562 | |||||||
| chr2:69361762 | T | A | 1 | a0001c0001t0001g0335 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.349+1783A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361762 | |||||||
| chr2:69361948 | C | G | 1 | a0001c0001t0041g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.349+1597G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361948 | |||||||
| chr2:69362015 | C | T | 5 | a0001c0001t0005g0096 a0001c0001t0005g0097 a0001c0001t0005g0098 others(2): Show |
5 | NA18612.hp2 NA18939.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+1530G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362015 | |||||||
| chr2:69362066 | A | T | 1 | a0001c0002t0004g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.349+1479T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362066 | |||||||
| chr2:69362205 | C | T | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.349+1340G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362205 | |||||||
| chr2:69362299 | G | A | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+1246C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362299 | |||||||
| chr2:69362384 | T | C | 1 | a0001c0001t0030g0330 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.349+1161A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362384 | |||||||
| chr2:69362557 | G | A | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.349+988C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362557 | |||||||
| chr2:69362572 | C | T | 3 | a0001c0002t0006g0132 a0001c0002t0006g0133 a0001c0002t0006g0134 |
3 | NA18988.hp2 NA19002.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.349+973G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362572 | |||||||
| chr2:69362607 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.349+938G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362607 | |||||||
| chr2:69362747 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.349+798T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362747 | |||||||
| chr2:69362751 | C | T | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.349+794G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362751 | |||||||
| chr2:69362816 | A | T | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.349+729T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362816 | |||||||
| chr2:69362824 | T | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.349+721A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362824 | |||||||
| chr2:69362908 | A | C | 1 | a0001c0001t0002g0179 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.349+637T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362908 | |||||||
| chr2:69363011 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.349+534G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69363011 | |||||||
| chr2:69363017 | G | A | 1 | a0001c0001t0023g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.349+528C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69363017 | |||||||
| chr2:69363108 | T | C | 31 | a0001c0001t0002g0036 a0001c0001t0002g0094 a0001c0001t0002g0110 others(28): Show |
32 | HG02074.hp1 HG02280.hp1 HG02451.hp1 others(29): Show |
intron_variant | MODIFIER | c.349+437A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69363108 | |||||||
| chr2:69363207 | G | A | 41 | a0001c0002t0004g0003 a0001c0002t0004g0127 a0001c0002t0004g0128 others(38): Show |
44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.349+338C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69363207 | |||||||
| chr2:69363682 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.224-12C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363682 | |||||||
| chr2:69363725 | C | T | 4 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(1): Show |
4 | HG01109.hp2 HG01928.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-55G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363725 | |||||||
| chr2:69363801 | C | T | 19 | a0001c0001t0002g0094 a0001c0001t0005g0010 a0001c0001t0005g0092 others(16): Show |
20 | HG02074.hp1 HG02602.hp2 HG04199.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-131G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363801 | |||||||
| chr2:69363809 | A | C | 1 | a0001c0001t0001g0261 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.224-139T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363809 | |||||||
| chr2:69363869 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.224-199G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363869 | |||||||
| chr2:69363891 | G | C | 1 | a0001c0001t0002g0024 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.224-221C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363891 | |||||||
| chr2:69363965 | A | C | 1 | a0001c0001t0002g0166 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.224-295T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363965 | |||||||
| chr2:69363989 | C | A | 1 | a0001c0001t0012g0034 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.224-319G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363989 | |||||||
| chr2:69364032 | C | T | 337 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(334): Show |
362 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.224-362G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364032 | |||||||
| chr2:69364070 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.224-400T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364070 | |||||||
| chr2:69364114 | C | CA | 97 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(94): Show |
103 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.224-445dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364114 | |||||||
| chr2:69364114 | C | CAA | 7 | a0001c0001t0002g0042 a0001c0001t0015g0038 a0001c0001t0015g0039 others(4): Show |
7 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.224-446_224-445dup others(2): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364114 | |||||||
| chr2:69364188 | C | T | 90 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(87): Show |
97 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.224-518G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364188 | |||||||
| chr2:69364540 | C | A | 3 | a0001c0002t0039g0152 a0001c0002t0053g0138 a0001c0002t0054g0151 |
3 | NA18942.hp2 NA19078.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.224-870G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364540 | |||||||
| chr2:69364636 | G | A | 3 | a0001c0001t0001g0335 a0001c0001t0002g0033 a0001c0001t0030g0330 |
3 | HG02145.hp1 HG02723.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.224-966C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364636 | |||||||
| chr2:69364738 | T | C | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.224-1068A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364738 | |||||||
| chr2:69364744 | C | G | 4 | a0001c0001t0002g0161 a0001c0001t0002g0178 a0001c0001t0002g0213 others(1): Show |
4 | NA18953.hp1 NA18955.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-1074G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364744 | |||||||
| chr2:69364784 | C | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0162 a0001c0001t0002g0224 |
4 | NA18969.hp2 NA18993.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-1114G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364784 | |||||||
| chr2:69364811 | A | G | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.224-1141T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364811 | |||||||
| chr2:69364864 | G | A | 1 | a0001c0001t0013g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.224-1194C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364864 | |||||||
| chr2:69364910 | G | A | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.224-1240C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364910 | |||||||
| chr2:69364982 | G | A | 93 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(90): Show |
100 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.224-1312C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364982 | |||||||
| chr2:69364994 | C | CA | 145 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0255 others(142): Show |
159 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.224-1325dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364994 | |||||||
| chr2:69364994 | C | CAA | 78 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0301 others(75): Show |
81 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.224-1326_224-1325d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364994 | |||||||
| chr2:69364994 | C | CAAA | 20 | a0001c0001t0002g0026 a0001c0001t0002g0036 a0001c0001t0002g0042 others(17): Show |
20 | HG01109.hp2 HG02015.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.224-1327_224-1325d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364994 | |||||||
| chr2:69364994 | C | CAAAA | 12 | a0001c0001t0025g0023 a0001c0002t0006g0016 a0001c0002t0006g0126 others(9): Show |
13 | HG00609.hp1 HG00621.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.224-1328_224-1325d others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364994 | |||||||
| chr2:69364994 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0020g0122 a0001c0001t0020g0123 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.224-1335_224-1325d others(13): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364994 | |||||||
| chr2:69365094 | T | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.224-1424A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365094 | |||||||
| chr2:69365111 | C | T | 3 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0048 |
3 | HG02559.hp1 HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.224-1441G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365111 | |||||||
| chr2:69365201 | A | G | 237 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(234): Show |
251 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.224-1531T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365201 | |||||||
| chr2:69365299 | G | A | 41 | a0001c0001t0026g0168 a0001c0002t0004g0003 a0001c0002t0004g0127 others(38): Show |
44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.224-1629C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365299 | |||||||
| chr2:69365360 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.224-1690A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365360 | |||||||
| chr2:69365466 | C | T | 233 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(230): Show |
247 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.224-1796G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365466 | |||||||
| chr2:69365529 | A | T | 239 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(236): Show |
253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.224-1859T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365529 | |||||||
| chr2:69365678 | T | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.224-2008A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365678 | |||||||
| chr2:69365752 | A | G | 233 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(230): Show |
247 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.224-2082T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365752 | |||||||
| chr2:69365808 | C | T | 233 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(230): Show |
247 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.224-2138G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365808 | |||||||
| chr2:69365957 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.224-2287G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365957 | |||||||
| chr2:69365959 | C | T | 1 | a0001c0002t0004g0137 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.224-2289G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365959 | |||||||
| chr2:69365960 | G | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0311 a0001c0001t0001g0312 |
3 | HG00558.hp2 NA19087.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.224-2290C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365960 | |||||||
| chr2:69366142 | A | AATTAAAG others(14): Show |
7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.224-2493_224-2473d others(23): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366142 | |||||||
| chr2:69366182 | C | T | 233 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(230): Show |
247 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.224-2512G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366182 | |||||||
| chr2:69366243 | C | T | 11 | a0001c0002t0006g0016 a0001c0002t0006g0132 a0001c0002t0006g0133 others(8): Show |
12 | HG00621.hp1 HG02015.hp1 NA18943.hp1 others(9): Show |
intron_variant | MODIFIER | c.224-2573G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366243 | |||||||
| chr2:69366259 | G | T | 181 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(178): Show |
192 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.224-2589C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366259 | |||||||
| chr2:69366261 | T | C | 242 | a0001c0001t0001g0291 a0001c0001t0002g0004 a0001c0001t0002g0011 others(239): Show |
256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.224-2591A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366261 | |||||||
| chr2:69366638 | A | G | 1 | a0001c0001t0001g0327 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.224-2968T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366638 | |||||||
| chr2:69366672 | C | T | 1 | a0001c0002t0004g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.224-3002G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366672 | |||||||
| chr2:69367152 | G | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+2849C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367152 | |||||||
| chr2:69367166 | G | C | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.223+2835C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367166 | |||||||
| chr2:69367208 | T | C | 2 | a0001c0001t0034g0247 a0001c0001t0056g0339 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.223+2793A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367208 | |||||||
| chr2:69367215 | G | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.223+2786C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367215 | |||||||
| chr2:69367344 | T | TTTG | 126 | a0001c0001t0001g0264 a0001c0001t0002g0004 a0001c0001t0002g0011 others(123): Show |
134 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.223+2654_223+2656d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367344 | |||||||
| chr2:69367344 | T | TTTGTTG | 12 | a0001c0001t0002g0056 a0001c0001t0009g0044 a0001c0001t0009g0045 others(9): Show |
12 | HG01433.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.223+2651_223+2656d others(8): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367344 | |||||||
| chr2:69367344 | T | TTTGTTGT others(2): Show |
42 | a0001c0001t0026g0168 a0001c0002t0004g0003 a0001c0002t0004g0127 others(39): Show |
45 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.223+2648_223+2656d others(11): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367344 | |||||||
| chr2:69367344 | T | TTTGTTGT others(11): Show |
1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.223+2639_223+2656d others(20): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367344 | |||||||
| chr2:69367347 | G | T | 47 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(44): Show |
50 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.223+2654C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367347 | |||||||
| chr2:69367350 | G | T | 1 | a0001c0001t0003g0071 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.223+2651C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367350 | |||||||
| chr2:69367521 | C | T | 5 | a0001c0001t0002g0042 a0001c0001t0015g0038 a0001c0001t0015g0039 others(2): Show |
5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+2480G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367521 | |||||||
| chr2:69367522 | G | A | 6 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+2479C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367522 | |||||||
| chr2:69367564 | T | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.223+2437A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367564 | |||||||
| chr2:69367585 | A | T | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.223+2416T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367585 | |||||||
| chr2:69367657 | G | A | 1 | a0001c0001t0001g0313 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.223+2344C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367657 | |||||||
| chr2:69367724 | G | C | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+2277C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367724 | |||||||
| chr2:69367842 | T | C | 1 | a0001c0001t0009g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.223+2159A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367842 | |||||||
| chr2:69368210 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.223+1791T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368210 | |||||||
| chr2:69368256 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(2): Show |
5 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1745C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368256 | |||||||
| chr2:69368308 | G | C | 1 | a0001c0001t0002g0204 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.223+1693C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368308 | |||||||
| chr2:69368470 | G | A | 1 | a0001c0002t0039g0152 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.223+1531C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368470 | |||||||
| chr2:69368545 | T | C | 8 | a0001c0001t0001g0255 a0001c0001t0001g0292 a0001c0001t0001g0294 others(5): Show |
8 | HG02165.hp2 NA18952.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+1456A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368545 | |||||||
| chr2:69368556 | C | T | 4 | a0001c0001t0011g0118 a0001c0001t0011g0119 a0001c0001t0011g0120 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+1445G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368556 | |||||||
| chr2:69368590 | T | G | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.223+1411A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368590 | |||||||
| chr2:69368598 | C | A | 1 | a0001c0001t0001g0299 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.223+1403G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368598 | |||||||
| chr2:69368708 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.223+1293C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368708 | |||||||
| chr2:69368715 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223+1286G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368715 | |||||||
| chr2:69368716 | G | A | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.223+1285C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368716 | |||||||
| chr2:69368718 | G | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.223+1283C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368718 | |||||||
| chr2:69368784 | T | C | 2 | a0001c0001t0002g0015 a0001c0001t0002g0207 |
3 | HG02257.hp1 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.223+1217A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368784 | |||||||
| chr2:69369060 | T | C | 237 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(234): Show |
251 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.223+941A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369060 | |||||||
| chr2:69369247 | A | G | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+754T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369247 | |||||||
| chr2:69369369 | A | T | 1 | a0001c0001t0018g0176 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.223+632T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369369 | |||||||
| chr2:69369537 | G | A | 1 | a0001c0002t0004g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.223+464C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369537 | |||||||
| chr2:69369662 | A | G | 1 | a0001c0001t0003g0063 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.223+339T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369662 | |||||||
| chr2:69369932 | T | TA | 42 | a0001c0001t0026g0168 a0001c0002t0004g0003 a0001c0002t0004g0127 others(39): Show |
45 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.223+68dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369932 | |||||||
| chr2:69369996 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG04204.hp1 | splice_region_variant&intron_variant | LOW | c.223+5C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369996 | |||||||
| chr2:69370335 | G | A | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.116-227C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69370335 | |||||||
| chr2:69370417 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.116-309C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69370417 | |||||||
| chr2:69370472 | C | G | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.116-364G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69370472 | |||||||
| chr2:69370694 | G | C | 182 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(179): Show |
193 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.116-586C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69370694 | |||||||
| chr2:69371076 | C | CT | 42 | a0001c0001t0001g0317 a0001c0001t0002g0094 a0001c0001t0002g0213 others(39): Show |
46 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.116-969dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371076 | |||||||
| chr2:69371076 | CT | C | 8 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0313 others(5): Show |
8 | HG02015.hp1 HG02717.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-969delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371076 | |||||||
| chr2:69371081 | T | C | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-973A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371081 | |||||||
| chr2:69371082 | T | C | 1 | a0001c0001t0015g0040 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.116-974A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371082 | |||||||
| chr2:69371111 | C | T | 233 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(230): Show |
247 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.116-1003G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371111 | |||||||
| chr2:69371130 | G | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-1022C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371130 | |||||||
| chr2:69371226 | C | A | 1 | a0001c0001t0001g0302 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.116-1118G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371226 | |||||||
| chr2:69371242 | AT | A | 7 | a0001c0001t0001g0306 a0001c0001t0001g0329 a0001c0001t0002g0224 others(4): Show |
7 | HG00558.hp1 HG01243.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.116-1135delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371242 | |||||||
| chr2:69371371 | G | T | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.116-1263C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371371 | |||||||
| chr2:69371374 | C | T | 1 | a0001c0001t0030g0330 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.116-1266G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371374 | |||||||
| chr2:69371424 | T | A | 233 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(230): Show |
247 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.116-1316A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371424 | |||||||
| chr2:69371483 | A | G | 3 | a0001c0002t0004g0127 a0001c0002t0004g0128 a0001c0002t0004g0129 |
3 | NA18956.hp1 NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.116-1375T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371483 | |||||||
| chr2:69371556 | G | A | 233 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(230): Show |
247 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.116-1448C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371556 | |||||||
| chr2:69371560 | G | A | 10 | a0001c0001t0002g0004 a0001c0001t0002g0232 a0001c0001t0002g0234 others(7): Show |
12 | HG01258.hp1 HG01928.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.116-1452C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371560 | |||||||
| chr2:69371563 | C | T | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.116-1455G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371563 | |||||||
| chr2:69371691 | G | T | 1 | a0001c0001t0002g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.116-1583C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371691 | |||||||
| chr2:69371694 | G | A | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.116-1586C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371694 | |||||||
| chr2:69371762 | G | A | 1 | a0001c0001t0002g0205 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.116-1654C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371762 | |||||||
| chr2:69371763 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.116-1655C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371763 | |||||||
| chr2:69371766 | G | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.116-1658C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371766 | |||||||
| chr2:69371794 | G | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-1686C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371794 | |||||||
| chr2:69371892 | A | C | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.116-1784T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371892 | |||||||
| chr2:69372082 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.115+1924G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372082 | |||||||
| chr2:69372095 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.115+1911C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372095 | |||||||
| chr2:69372198 | C | CA | 19 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(16): Show |
19 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.115+1807dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372198 | |||||||
| chr2:69372198 | CA | C | 9 | a0001c0001t0002g0094 a0001c0001t0002g0116 a0001c0001t0007g0031 others(6): Show |
9 | HG02257.hp2 HG02258.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+1807delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372198 | |||||||
| chr2:69372216 | A | G | 48 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(45): Show |
51 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.115+1790T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372216 | |||||||
| chr2:69372495 | G | A | 12 | a0001c0001t0001g0252 a0001c0001t0001g0308 a0001c0001t0001g0309 others(9): Show |
12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.115+1511C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372495 | |||||||
| chr2:69372784 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.115+1222T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372784 | |||||||
| chr2:69373039 | G | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+967C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373039 | |||||||
| chr2:69373051 | A | G | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.115+955T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373051 | |||||||
| chr2:69373093 | C | T | 2 | a0001c0001t0019g0124 a0001c0001t0019g0125 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.115+913G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373093 | |||||||
| chr2:69373178 | T | G | 1 | a0001c0001t0002g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.115+828A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373178 | |||||||
| chr2:69373252 | C | T | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+754G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373252 | |||||||
| chr2:69373303 | T | C | 35 | a0001c0001t0002g0036 a0001c0001t0002g0094 a0001c0001t0002g0110 others(32): Show |
36 | HG02074.hp1 HG02280.hp1 HG02451.hp1 others(33): Show |
intron_variant | MODIFIER | c.115+703A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373303 | |||||||
| chr2:69373334 | T | A | 239 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(236): Show |
253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.115+672A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373334 | |||||||
| chr2:69373337 | G | A | 2 | a0001c0001t0003g0035 a0001c0001t0003g0086 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.115+669C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373337 | |||||||
| chr2:69373369 | C | A | 8 | a0001c0001t0002g0036 a0001c0001t0002g0110 a0001c0001t0002g0112 others(5): Show |
8 | HG02572.hp1 HG02922.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+637G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373369 | |||||||
| chr2:69373434 | T | C | 1 | a0001c0002t0004g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.115+572A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373434 | |||||||
| chr2:69373522 | C | T | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+484G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373522 | |||||||
| chr2:69373551 | C | T | 131 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(128): Show |
139 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.115+455G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373551 | |||||||
| chr2:69373559 | T | C | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.115+447A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373559 | |||||||
| chr2:69373655 | G | A | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.115+351C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373655 | |||||||
| chr2:69373714 | A | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.115+292T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373714 | |||||||
| chr2:69373772 | T | C | 2 | a0001c0001t0002g0056 a0001c0001t0012g0034 |
2 | HG01433.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.115+234A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373772 | |||||||
| chr2:69373956 | G | A | 1 | a0001c0001t0034g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.115+50C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373956 | |||||||
| chr2:69374319 | C | CT | 228 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(225): Show |
242 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(239): Show |
intron_variant | MODIFIER | c.8-207dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374319 | |||||||
| chr2:69374370 | G | A | 93 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(90): Show |
100 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.8-257C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374370 | |||||||
| chr2:69374400 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.8-287C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374400 | |||||||
| chr2:69374460 | C | T | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-347G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374460 | |||||||
| chr2:69374577 | T | C | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.8-464A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374577 | |||||||
| chr2:69374793 | C | T | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-680G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374793 | |||||||
| chr2:69374860 | G | A | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.8-747C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374860 | |||||||
| chr2:69375062 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.8-949A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375062 | |||||||
| chr2:69375105 | A | G | 1 | a0001c0001t0013g0022 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.8-992T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375105 | |||||||
| chr2:69375137 | T | C | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.8-1024A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375137 | |||||||
| chr2:69375247 | T | A | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.8-1134A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375247 | |||||||
| chr2:69375252 | TA | T | 93 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(90): Show |
100 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.8-1140delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375252 | |||||||
| chr2:69375325 | A | G | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1212T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375325 | |||||||
| chr2:69375343 | T | C | 1 | a0001c0002t0006g0126 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.8-1230A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375343 | |||||||
| chr2:69375355 | C | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-1242G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375355 | |||||||
| chr2:69375437 | C | A | 3 | a0001c0001t0020g0122 a0001c0001t0020g0123 a0001c0001t0038g0243 |
3 | HG01167.hp2 HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.8-1324G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375437 | |||||||
| chr2:69375501 | T | C | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.8-1388A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375501 | |||||||
| chr2:69375676 | C | T | 1 | a0001c0001t0013g0022 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.8-1563G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375676 | |||||||
| chr2:69375952 | C | T | 238 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(235): Show |
252 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.8-1839G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375952 | |||||||
| chr2:69376017 | C | T | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.8-1904G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376017 | |||||||
| chr2:69376043 | T | C | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-1930A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376043 | |||||||
| chr2:69376131 | C | T | 129 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(126): Show |
137 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.8-2018G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376131 | |||||||
| chr2:69376132 | G | C | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.8-2019C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376132 | |||||||
| chr2:69376324 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.8-2211G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376324 | |||||||
| chr2:69376340 | G | A | 4 | a0001c0001t0011g0118 a0001c0001t0011g0119 a0001c0001t0011g0120 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-2227C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376340 | |||||||
| chr2:69376379 | C | T | 1 | a0001c0001t0011g0118 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8-2266G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376379 | |||||||
| chr2:69376429 | T | C | 3 | a0001c0001t0001g0314 a0001c0001t0001g0324 a0001c0001t0001g0327 |
3 | HG00544.hp1 HG02080.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.8-2316A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376429 | |||||||
| chr2:69376467 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.8-2354G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376467 | |||||||
| chr2:69376470 | G | A | 1 | a0001c0001t0034g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.8-2357C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376470 | |||||||
| chr2:69376491 | C | G | 2 | a0001c0001t0013g0051 a0001c0001t0013g0089 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.8-2378G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376491 | |||||||
| chr2:69376523 | G | GA | 166 | a0001c0001t0001g0315 a0001c0001t0002g0004 a0001c0001t0002g0011 others(163): Show |
177 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.8-2411dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376523 | |||||||
| chr2:69376540 | G | GA | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-2428dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376540 | |||||||
| chr2:69376572 | C | A | 1 | a0001c0001t0002g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.8-2459G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376572 | |||||||
| chr2:69376603 | G | A | 15 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.8-2490C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376603 | |||||||
| chr2:69376611 | A | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-2498T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376611 | |||||||
| chr2:69376645 | G | A | 1 | a0001c0005t0001g0316 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.8-2532C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376645 | |||||||
| chr2:69376651 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.8-2538A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376651 | |||||||
| chr2:69376782 | G | C | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-2669C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376782 | |||||||
| chr2:69376948 | G | A | 1 | a0002c0004t0001g0320 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.8-2835C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376948 | |||||||
| chr2:69377086 | C | T | 239 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(236): Show |
253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.8-2973G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377086 | |||||||
| chr2:69377207 | C | CA | 208 | a0001c0001t0001g0257 a0001c0001t0001g0318 a0001c0001t0001g0319 others(205): Show |
221 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(218): Show |
intron_variant | MODIFIER | c.8-3095dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377207 | |||||||
| chr2:69377207 | C | CAA | 16 | a0001c0001t0002g0110 a0001c0001t0002g0230 a0001c0001t0003g0064 others(13): Show |
16 | HG00735.hp2 HG01884.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-3096_8-3095dupTT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377207 | |||||||
| chr2:69377285 | T | G | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.8-3172A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377285 | |||||||
| chr2:69377313 | A | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-3200T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377313 | |||||||
| chr2:69377417 | G | A | 1 | a0001c0001t0049g0111 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.8-3304C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377417 | |||||||
| chr2:69377492 | T | TAC | 14 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0222 others(11): Show |
14 | HG01255.hp2 HG02109.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.8-3380_8-3379insGT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377492 | |||||||
| chr2:69377493 | A | AC | 213 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(210): Show |
227 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(224): Show |
intron_variant | MODIFIER | c.8-3381_8-3380insG | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377493 | |||||||
| chr2:69377494 | A | C | 11 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0063 others(8): Show |
11 | HG00558.hp1 HG02071.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.8-3381T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377494 | |||||||
| chr2:69377498 | T | A | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.8-3385A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377498 | |||||||
| chr2:69377503 | A | T | 2 | a0001c0001t0034g0247 a0001c0001t0056g0339 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.8-3390T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377503 | |||||||
| chr2:69377538 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.8-3425A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377538 | |||||||
| chr2:69377568 | G | A | 3 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0002g0212 |
3 | HG00438.hp2 NA18954.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.8-3455C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377568 | |||||||
| chr2:69377590 | GC | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-3478delG | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377590 | |||||||
| chr2:69377645 | G | A | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-3532C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377645 | |||||||
| chr2:69377765 | C | A | 5 | a0001c0001t0002g0042 a0001c0001t0015g0038 a0001c0001t0015g0039 others(2): Show |
5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-3652G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377765 | |||||||
| chr2:69377795 | A | G | 15 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.8-3682T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377795 | |||||||
| chr2:69377928 | A | T | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-3815T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377928 | |||||||
| chr2:69378056 | C | A | 2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | NA18953.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.8-3943G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378056 | |||||||
| chr2:69378067 | G | A | 3 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0001c0001t0007g0043 |
3 | HG02258.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.8-3954C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378067 | |||||||
| chr2:69378154 | G | A | 1 | a0001c0001t0001g0323 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.8-4041C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378154 | |||||||
| chr2:69378157 | G | A | 1 | a0001c0001t0005g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.8-4044C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378157 | |||||||
| chr2:69378174 | T | C | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.8-4061A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378174 | |||||||
| chr2:69378416 | T | C | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.8-4303A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378416 | |||||||
| chr2:69378420 | T | A | 234 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(231): Show |
248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.8-4307A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378420 | |||||||
| chr2:69378485 | G | T | 2 | a0001c0001t0005g0092 a0001c0001t0005g0093 |
2 | NA18966.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.8-4372C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378485 | |||||||
| chr2:69378498 | C | T | 1 | a0001c0001t0034g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.8-4385G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378498 | |||||||
| chr2:69378692 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.8-4579G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378692 | |||||||
| chr2:69378944 | C | A | 4 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-4831G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378944 | |||||||
| chr2:69379068 | G | A | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-4955C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379068 | |||||||
| chr2:69379071 | C | T | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.8-4958G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379071 | |||||||
| chr2:69379204 | C | T | 94 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(91): Show |
101 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.8-5091G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379204 | |||||||
| chr2:69379388 | G | A | 2 | a0001c0001t0003g0035 a0001c0001t0003g0086 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.8-5275C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379388 | |||||||
| chr2:69379515 | T | A | 38 | a0001c0002t0004g0003 a0001c0002t0004g0131 a0001c0002t0004g0137 others(35): Show |
41 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.8-5402A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379515 | |||||||
| chr2:69379540 | ATTTTC | A | 41 | a0001c0002t0004g0003 a0001c0002t0004g0127 a0001c0002t0004g0128 others(38): Show |
44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.8-5432_8-5428delGA others(3): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379540 | |||||||
| chr2:69379585 | T | C | 1 | a0001c0001t0002g0215 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.8-5472A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379585 | |||||||
| chr2:69379686 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.8-5573A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379686 | |||||||
| chr2:69379715 | T | C | 4 | a0001c0001t0013g0022 a0001c0001t0013g0051 a0001c0001t0013g0089 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-5602A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379715 | |||||||
| chr2:69379717 | T | G | 1 | a0001c0001t0024g0049 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8-5604A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379717 | |||||||
| chr2:69379779 | T | G | 1 | a0001c0001t0044g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.8-5666A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379779 | |||||||
| chr2:69379971 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.8-5858C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379971 | |||||||
| chr2:69380163 | C | A | 1 | a0001c0001t0001g0324 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.8-6050G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380163 | |||||||
| chr2:69380245 | A | G | 239 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(236): Show |
253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.8-6132T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380245 | |||||||
| chr2:69380260 | C | T | 1 | a0001c0001t0005g0091 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.8-6147G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380260 | |||||||
| chr2:69380268 | T | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-6155A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380268 | |||||||
| chr2:69380313 | G | A | 6 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-6200C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380313 | |||||||
| chr2:69380507 | T | C | 2 | a0001c0001t0019g0124 a0001c0001t0019g0125 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.8-6394A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380507 | |||||||
| chr2:69380514 | T | C | 3 | a0001c0001t0007g0031 a0001c0001t0007g0032 a0001c0001t0007g0043 |
3 | HG02258.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.8-6401A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380514 | |||||||
| chr2:69380615 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7+6450C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380615 | |||||||
| chr2:69380768 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7+6297G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380768 | |||||||
| chr2:69380879 | C | G | 1 | a0001c0002t0004g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.7+6186G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380879 | |||||||
| chr2:69381011 | G | A | 1 | a0001c0001t0003g0088 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.7+6054C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381011 | |||||||
| chr2:69381041 | G | A | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7+6024C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381041 | |||||||
| chr2:69381098 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+5967C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381098 | |||||||
| chr2:69381246 | G | C | 1 | a0001c0001t0010g0217 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.7+5819C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381246 | |||||||
| chr2:69381262 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.7+5803G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381262 | |||||||
| chr2:69381344 | C | G | 14 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0053 others(11): Show |
16 | HG02056.hp2 HG02135.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.7+5721G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381344 | |||||||
| chr2:69381408 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7+5657A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381408 | |||||||
| chr2:69381539 | C | T | 2 | a0001c0001t0034g0247 a0001c0001t0056g0339 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.7+5526G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381539 | |||||||
| chr2:69381556 | C | CT | 7 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(4): Show |
7 | HG00609.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+5508dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381556 | |||||||
| chr2:69381556 | CT | C | 17 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0002g0024 others(14): Show |
17 | HG01069.hp1 HG01069.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.7+5508delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381556 | |||||||
| chr2:69381720 | A | AT | 231 | a0001c0001t0001g0250 a0001c0001t0002g0004 a0001c0001t0002g0011 others(228): Show |
245 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.7+5344dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381720 | |||||||
| chr2:69381839 | C | A | 1 | a0001c0001t0002g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7+5226G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381839 | |||||||
| chr2:69381863 | C | CT | 226 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(223): Show |
240 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.7+5201dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381863 | |||||||
| chr2:69381863 | C | CTT | 6 | a0001c0001t0002g0161 a0001c0001t0003g0059 a0001c0001t0003g0060 others(3): Show |
6 | HG01175.hp1 HG01515.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+5200_7+5201dupAA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381863 | |||||||
| chr2:69381870 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.7+5195A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381870 | |||||||
| chr2:69382061 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7+5004C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69382061 | |||||||
| chr2:69382501 | T | C | 31 | a0001c0001t0002g0036 a0001c0001t0002g0094 a0001c0001t0002g0110 others(28): Show |
32 | HG02074.hp1 HG02280.hp1 HG02451.hp1 others(29): Show |
intron_variant | MODIFIER | c.7+4564A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69382501 | |||||||
| chr2:69382671 | T | C | 1 | a0001c0002t0004g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.7+4394A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69382671 | |||||||
| chr2:69382831 | A | T | 337 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(334): Show |
362 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.7+4234T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69382831 | |||||||
| chr2:69382849 | C | T | 48 | a0001c0001t0002g0033 a0001c0001t0009g0044 a0001c0001t0009g0045 others(45): Show |
51 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.7+4216G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69382849 | |||||||
| chr2:69382972 | A | G | 94 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(91): Show |
101 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.7+4093T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69382972 | |||||||
| chr2:69383049 | A | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.7+4016T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383049 | |||||||
| chr2:69383095 | G | C | 1 | a0001c0001t0034g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7+3970C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383095 | |||||||
| chr2:69383371 | A | T | 1 | a0001c0001t0002g0160 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.7+3694T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383371 | |||||||
| chr2:69383585 | T | A | 4 | a0001c0001t0019g0124 a0001c0001t0019g0125 a0001c0001t0020g0122 others(1): Show |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+3480A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383585 | |||||||
| chr2:69383601 | C | CATTT | 5 | a0001c0001t0002g0042 a0001c0001t0015g0038 a0001c0001t0015g0039 others(2): Show |
5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+3460_7+3463dupAA others(2): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383601 | |||||||
| chr2:69383689 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.7+3376A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383689 | |||||||
| chr2:69383733 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0257 others(2): Show |
9 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+3332G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383733 | |||||||
| chr2:69383805 | T | C | 1 | a0001c0001t0030g0330 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7+3260A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383805 | |||||||
| chr2:69383977 | C | T | 1 | a0001c0001t0001g0331 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.7+3088G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383977 | |||||||
| chr2:69384138 | CTTCTCTG others(18): Show |
C | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2902_7+2926delTA others(23): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384138 | |||||||
| chr2:69384199 | A | G | 1 | a0001c0001t0044g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.7+2866T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384199 | |||||||
| chr2:69384353 | C | T | 238 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(235): Show |
252 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.7+2712G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384353 | |||||||
| chr2:69384540 | C | G | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2525G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384540 | |||||||
| chr2:69384541 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2524T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384541 | |||||||
| chr2:69384556 | G | C | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2509C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384556 | |||||||
| chr2:69384557 | C | A | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2508G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384557 | |||||||
| chr2:69384572 | T | G | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2493A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384572 | |||||||
| chr2:69384580 | T | G | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2485A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384580 | |||||||
| chr2:69384619 | C | T | 1 | a0001c0001t0013g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.7+2446G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384619 | |||||||
| chr2:69384620 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2445C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384620 | |||||||
| chr2:69384650 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7+2415A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384650 | |||||||
| chr2:69384654 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2411C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384654 | |||||||
| chr2:69384655 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2410G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384655 | |||||||
| chr2:69384657 | G | C | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2408C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384657 | |||||||
| chr2:69384658 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2407G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384658 | |||||||
| chr2:69384673 | G | A | 1 | a0001c0002t0006g0159 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.7+2392C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384673 | |||||||
| chr2:69384681 | G | A | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+2384C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384681 | |||||||
| chr2:69384693 | C | CA | 7 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0334 others(4): Show |
7 | HG02074.hp2 HG02602.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+2371dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384693 | |||||||
| chr2:69384693 | CA | C | 7 | a0001c0001t0001g0255 a0001c0001t0011g0118 a0001c0001t0011g0119 others(4): Show |
7 | HG01243.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+2371delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384693 | |||||||
| chr2:69384693 | CAA | C | 6 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0002g0241 others(3): Show |
6 | HG02109.hp2 HG02717.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+2370_7+2371delTT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384693 | |||||||
| chr2:69384693 | CAAA | C | 175 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(172): Show |
186 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.7+2369_7+2371delTT others(1): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384693 | |||||||
| chr2:69384693 | CAAAAAAA others(3): Show |
C | 48 | a0001c0001t0002g0033 a0001c0001t0009g0044 a0001c0001t0009g0045 others(45): Show |
51 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.7+2362_7+2371delTT others(8): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384693 | |||||||
| chr2:69384745 | A | G | 7 | a0001c0001t0007g0027 a0001c0001t0007g0028 a0001c0001t0007g0029 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+2320T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384745 | |||||||
| chr2:69384764 | GAAGAAAG others(7): Show |
G | 1 | a0001c0001t0033g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.7+2287_7+2300delTT others(12): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384764 | |||||||
| chr2:69384777 | A | AAAAG | 39 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(36): Show |
42 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.7+2284_7+2287dupCT others(2): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384777 | |||||||
| chr2:69384791 | AAG | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.7+2272_7+2273delCT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384791 | |||||||
| chr2:69384875 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7+2190A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384875 | |||||||
| chr2:69384987 | A | G | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7+2078T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384987 | |||||||
| chr2:69385411 | C | G | 241 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(238): Show |
255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.7+1654G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385411 | |||||||
| chr2:69385426 | C | T | 238 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(235): Show |
252 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.7+1639G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385426 | |||||||
| chr2:69385523 | C | T | 5 | a0001c0001t0002g0042 a0001c0001t0015g0038 a0001c0001t0015g0039 others(2): Show |
5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+1542G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385523 | |||||||
| chr2:69385539 | TA | T | 6 | a0001c0001t0002g0042 a0001c0001t0007g0032 a0001c0001t0015g0038 others(3): Show |
6 | HG01243.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+1525delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385539 | |||||||
| chr2:69385539 | TATTTA | T | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(34): Show |
40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.7+1521_7+1525delTA others(3): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385539 | |||||||
| chr2:69385543 | TA | T | 140 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0014 others(137): Show |
149 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.7+1521delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385543 | |||||||
| chr2:69385544 | A | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0269 a0001c0001t0001g0309 others(9): Show |
12 | HG00609.hp2 HG00735.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.7+1521T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385544 | |||||||
| chr2:69385544 | AT | A | 50 | a0001c0001t0002g0004 a0001c0001t0002g0036 a0001c0001t0002g0094 others(47): Show |
52 | HG00741.hp2 HG01069.hp2 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.7+1520delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385544 | |||||||
| chr2:69385548 | T | A | 1 | a0001c0001t0056g0339 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7+1517A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385548 | |||||||
| chr2:69385549 | T | A | 10 | a0001c0001t0002g0004 a0001c0001t0002g0232 a0001c0001t0002g0234 others(7): Show |
12 | HG01258.hp1 HG01928.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.7+1516A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385549 | |||||||
| chr2:69385746 | A | G | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | NA18948.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.7+1319T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385746 | |||||||
| chr2:69385853 | C | CT | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.7+1211dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385853 | |||||||
| chr2:69386027 | T | TA | 129 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(126): Show |
139 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.7+1037dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386027 | |||||||
| chr2:69386027 | TA | T | 13 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(10): Show |
13 | HG00558.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.7+1037delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386027 | |||||||
| chr2:69386215 | T | A | 1 | a0001c0001t0002g0241 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.7+850A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386215 | |||||||
| chr2:69386286 | C | T | 236 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(233): Show |
250 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(247): Show |
intron_variant | MODIFIER | c.7+779G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386286 | |||||||
| chr2:69386425 | A | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.7+640T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386425 | |||||||
| chr2:69386629 | T | A | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.7+436A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386629 | |||||||
| chr2:69386633 | T | A | 1 | a0001c0001t0038g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.7+432A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386633 | |||||||
| chr2:69386676 | G | T | 2 | a0001c0001t0034g0247 a0001c0001t0056g0339 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.7+389C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386676 | |||||||
| chr2:69386794 | T | C | 236 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(233): Show |
250 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(247): Show |
intron_variant | MODIFIER | c.7+271A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386794 | |||||||
| chr2:69386809 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.7+256C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386809 | |||||||
| chr2:69386826 | A | G | 242 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(239): Show |
256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.7+239T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386826 | |||||||
| chr2:69387025 | C | A | 4 | a0001c0002t0006g0016 a0001c0002t0006g0244 a0001c0002t0006g0245 others(1): Show |
5 | HG00621.hp1 NA18972.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+40G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69387025 | |||||||
| chr2:69387029 | A | G | 238 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(235): Show |
252 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.7+36T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69387029 |