| geneid | 9945 |
|---|---|
| ensemblid | ENSG00000131459.13 |
| hgncid | 4242 |
| symbol | GFPT2 |
| name | glutamine-fructose-6-phosphate transaminase 2 |
| refseq_nuc | NM_005110.4 |
| refseq_prot | NP_005101.1 |
| ensembl_nuc | ENST00000253778.13 |
| ensembl_prot | ENSP00000253778.8 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 180300698 |
| end | 180353336 |
| strand | - |
| ver | v1.2 |
| region | chr5:180300698-180353336 |
| region5000 | chr5:180295698-180358336 |
| regionname0 | GFPT2_chr5_180300698_180353336 |
| regionname5000 | GFPT2_chr5_180295698_180358336 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 682 | 288 | 87 | 52 | 104 | 13 | 30 | 77 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002 | 0/0 | 682 | 101 | 7 | 11 | 67 | 4 | 12 | 48 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0003 | 0/0 | 682 | 18 | 0 | 1 | 14 | 1 | 2 | 14 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0004 | 0/0 | 682 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0005 | 0/0 | 682 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0006 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2049 | 90 | 28 | 24 | 12 | 9 | 15 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0002 | 0/0 | 2049 | 89 | 4 | 11 | 61 | 3 | 10 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0003 | 0/0 | 2049 | 72 | 9 | 13 | 41 | 3 | 6 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0004 | 0/0 | 2049 | 60 | 14 | 10 | 27 | 1 | 8 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0005 | 0/0 | 2049 | 57 | 29 | 5 | 22 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0006 | 0/0 | 2049 | 14 | 0 | 1 | 10 | 1 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0007 | 0/0 | 2049 | 6 | 1 | 0 | 4 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0008 | 0/0 | 2049 | 3 | 0 | 0 | 1 | 0 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0009 | 0/0 | 2049 | 3 | 3 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0010 | 0/0 | 2049 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0011 | 0/0 | 2049 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0012 | 0/0 | 2049 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0013 | 0/0 | 2049 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0014 | 0/0 | 2049 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0015 | 0/0 | 2049 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0016 | 0/0 | 2039 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0017 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0018 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0019 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0020 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| c0021 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 986 | 118 | 30 | 18 | 47 | 6 | 16 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0002 | 0/1 | 977 | 114 | 23 | 29 | 44 | 8 | 9 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0003 | 0/0 | 986 | 67 | 3 | 11 | 43 | 3 | 7 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0004 | 0/0 | 986 | 21 | 12 | 1 | 8 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0005 | 0/0 | 986 | 14 | 0 | 1 | 13 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0006 | 0/0 | 977 | 14 | 9 | 0 | 1 | 1 | 3 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0007 | 0/0 | 986 | 10 | 0 | 0 | 10 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0008 | 0/0 | 986 | 8 | 0 | 5 | 3 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0009 | 0/0 | 977 | 8 | 0 | 0 | 6 | 0 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0010 | 0/0 | 986 | 5 | 0 | 0 | 3 | 0 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0011 | 0/0 | 977 | 4 | 4 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0012 | 0/0 | 986 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0013 | 0/0 | 998 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0014 | 0/0 | 977 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0015 | 0/0 | 977 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0016 | 0/0 | 977 | 2 | 0 | 1 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0017 | 0/0 | 965 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0018 | 0/0 | 986 | 2 | 0 | 0 | 0 | 0 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0019 | 0/0 | 977 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0020 | 0/0 | 968 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0021 | 0/0 | 986 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0022 | 0/0 | 977 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0023 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0024 | 0/0 | 986 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0025 | 0/0 | 986 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0026 | 0/0 | 977 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0027 | 0/0 | 977 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0028 | 0/0 | 977 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0029 | 0/0 | 965 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0030 | 0/0 | 965 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| t0031 | 0/0 | 977 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0281 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0389 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| g0390 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2049 | 90 | 28 | 24 | 12 | 9 | 15 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0003 | 0/0 | 2049 | 72 | 9 | 13 | 41 | 3 | 6 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0004 | 0/0 | 2049 | 60 | 14 | 10 | 27 | 1 | 8 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005 | 0/0 | 2049 | 57 | 29 | 5 | 22 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0009 | 0/0 | 2049 | 3 | 3 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0012 | 0/0 | 2049 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0017 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0018 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0019 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0021 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0002 | 0/0 | 2049 | 89 | 4 | 11 | 61 | 3 | 10 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0007 | 0/0 | 2049 | 6 | 1 | 0 | 4 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0008 | 0/0 | 2049 | 3 | 0 | 0 | 1 | 0 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0015 | 0/0 | 2049 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0020 | 0/0 | 2049 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0003c0006 | 0/0 | 2049 | 14 | 0 | 1 | 10 | 1 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0003c0013 | 0/0 | 2049 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0003c0014 | 0/0 | 2049 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0004c0011 | 0/0 | 2049 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0005c0010 | 0/0 | 2049 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0006c0016 | 0/0 | 2039 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3034 | 32 | 14 | 8 | 3 | 3 | 3 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0001t0002 | 0/1 | 3025 | 42 | 8 | 16 | 8 | 5 | 4 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0001t0006 | 0/0 | 3025 | 9 | 4 | 0 | 1 | 1 | 3 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0001t0010 | 0/0 | 3034 | 2 | 0 | 0 | 0 | 0 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0001t0014 | 0/0 | 3025 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0001t0018 | 0/0 | 3034 | 2 | 0 | 0 | 0 | 0 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0001t0021 | 0/0 | 3034 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0003t0001 | 0/0 | 3034 | 20 | 2 | 1 | 12 | 2 | 3 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0003t0002 | 0/0 | 3025 | 48 | 5 | 11 | 28 | 1 | 3 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0003t0006 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0003t0008 | 0/0 | 3034 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0003t0010 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0003t0026 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0004t0001 | 0/0 | 3034 | 43 | 7 | 8 | 20 | 1 | 7 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0004t0002 | 0/0 | 3025 | 8 | 4 | 2 | 1 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0004t0004 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0004t0006 | 0/0 | 3025 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0004t0010 | 0/0 | 3034 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0004t0013 | 0/0 | 3046 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0004t0024 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0004t0030 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0001 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0002 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0003 | 0/0 | 3034 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0004 | 0/0 | 3034 | 20 | 12 | 1 | 7 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0005 | 0/0 | 3034 | 13 | 0 | 1 | 12 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0006 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0008 | 0/0 | 3034 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0011 | 0/0 | 3025 | 4 | 4 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0015 | 0/0 | 3025 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0016 | 0/0 | 3025 | 2 | 0 | 1 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0017 | 0/0 | 3013 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0019 | 0/0 | 3025 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0023 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0027 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0029 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0005t0031 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0009t0001 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0009t0002 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0009t0006 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0012t0001 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0012t0002 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0017t0001 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0018t0028 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0019t0001 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0001c0021t0002 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0002t0001 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0002t0003 | 0/0 | 3034 | 62 | 3 | 7 | 42 | 3 | 7 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0002t0005 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0002t0007 | 0/0 | 3034 | 10 | 0 | 0 | 10 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0002t0008 | 0/0 | 3034 | 4 | 0 | 4 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0002t0009 | 0/0 | 3025 | 8 | 0 | 0 | 6 | 0 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0002t0020 | 0/0 | 3016 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0002t0022 | 0/0 | 3025 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0002t0025 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0007t0001 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0007t0002 | 0/0 | 3025 | 5 | 0 | 0 | 4 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0008t0001 | 0/0 | 3034 | 3 | 0 | 0 | 1 | 0 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0015t0001 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0002c0020t0002 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0003c0006t0001 | 0/0 | 3034 | 9 | 0 | 1 | 7 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0003c0006t0002 | 0/0 | 3025 | 2 | 0 | 0 | 0 | 1 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0003c0006t0012 | 0/0 | 3034 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0003c0013t0001 | 0/0 | 3034 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0003c0014t0002 | 0/0 | 3025 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0004c0011t0003 | 0/0 | 3034 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0005c0010t0002 | 0/0 | 3025 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| a0006c0016t0003 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | copy fasta | chr5 | 180295698 | 180358336 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0281 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0006g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0006g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0006g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0006g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0006g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0006g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0006g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0006g0389 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0006g0390 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0010g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0010g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0014g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0014g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0018g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0018g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0001t0021g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0006g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0008g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0010g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0003t0026g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0002g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0006g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0006g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0010g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0013g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0013g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0024g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0004t0030g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0006g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0008g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0008g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0011g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0011g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0011g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0011g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0015g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0015g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0016g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0016g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0017g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0017g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0019g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0019g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0023g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0027g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0029g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0005t0031g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0009t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0009t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0009t0006g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0012t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0012t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0017t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0018t0028g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0019t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0001c0021t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0007g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0008g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0008g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0009g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0009g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0009g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0009g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0009g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0009g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0009g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0009g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0020g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0022g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0002t0025g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0007t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0007t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0007t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0007t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0007t0002g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0008t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0008t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0008t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0015t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0002c0020t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0012g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0012g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0006t0012g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0013t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0013t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0014t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0003c0014t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0004c0011t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0005c0010t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0005c0010t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| a0006c0016t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0006 | t0002 | g0014 | EUR | GBR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0297 | EUR | GBR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00140 | hp1 | a0001 | c0003 | t0002 | g0303 | EUR | GBR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00140 | hp2 | a0002 | c0002 | t0003 | g0204 | EUR | GBR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0390 | EUR | FIN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0118 | EUR | FIN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0119 | EUR | FIN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0345 | EUR | FIN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0167 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00423 | hp2 | a0001 | c0004 | t0001 | g0180 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00438 | hp1 | a0002 | c0002 | t0003 | g0099 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00438 | hp2 | a0001 | c0004 | t0010 | g0050 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00544 | hp1 | a0002 | c0002 | t0003 | g0143 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0244 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00558 | hp2 | a0001 | c0003 | t0002 | g0318 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00597 | hp1 | a0002 | c0002 | t0003 | g0097 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00597 | hp2 | a0001 | c0003 | t0002 | g0269 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00609 | hp1 | a0001 | c0005 | t0005 | g0039 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00609 | hp2 | a0002 | c0002 | t0003 | g0121 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00621 | hp2 | a0002 | c0020 | t0002 | g0315 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0061 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00642 | hp1 | a0001 | c0005 | t0016 | g0306 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00642 | hp2 | a0001 | c0004 | t0001 | g0083 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00673 | hp1 | a0001 | c0005 | t0005 | g0043 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00673 | hp2 | a0001 | c0003 | t0001 | g0086 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0354 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0332 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01074 | hp1 | a0002 | c0002 | t0003 | g0123 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01074 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01099 | hp1 | a0002 | c0002 | t0008 | g0012 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01106 | hp1 | a0001 | c0004 | t0002 | g0365 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0350 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01109 | hp2 | a0002 | c0002 | t0008 | g0247 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0346 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01167 | hp2 | a0001 | c0005 | t0004 | g0222 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01175 | hp1 | a0001 | c0003 | t0002 | g0302 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01175 | hp2 | a0002 | c0002 | t0003 | g0111 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01192 | hp1 | a0001 | c0003 | t0008 | g0145 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0253 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01255 | hp2 | a0001 | c0004 | t0001 | g0110 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01257 | hp1 | a0002 | c0002 | t0003 | g0141 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01261 | hp1 | a0004 | c0011 | t0003 | g0008 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01346 | hp1 | a0002 | c0002 | t0003 | g0140 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01346 | hp2 | a0001 | c0004 | t0002 | g0276 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0355 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01358 | hp2 | a0001 | c0005 | t0003 | g0107 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01433 | hp1 | a0001 | c0003 | t0002 | g0286 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0356 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01496 | hp2 | a0004 | c0011 | t0003 | g0008 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01515 | hp1 | a0002 | c0007 | t0002 | g0364 | EUR | IBS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01516 | hp1 | a0002 | c0002 | t0003 | g0106 | EUR | IBS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | IBS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01884 | hp1 | a0001 | c0005 | t0002 | g0358 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01928 | hp2 | a0002 | c0002 | t0008 | g0248 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0343 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01934 | hp2 | a0001 | c0004 | t0001 | g0070 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01943 | hp1 | a0002 | c0002 | t0003 | g0154 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01952 | hp2 | a0001 | c0004 | t0001 | g0187 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01975 | hp1 | a0003 | c0006 | t0001 | g0233 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01978 | hp1 | a0001 | c0004 | t0001 | g0163 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01978 | hp2 | a0001 | c0005 | t0003 | g0134 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01981 | hp1 | a0001 | c0005 | t0005 | g0045 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01981 | hp2 | a0001 | c0003 | t0002 | g0294 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01993 | hp1 | a0001 | c0003 | t0002 | g0363 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01993 | hp2 | a0002 | c0002 | t0003 | g0136 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02004 | hp1 | a0002 | c0002 | t0008 | g0012 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0338 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0378 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02040 | hp1 | a0001 | c0005 | t0005 | g0040 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02040 | hp2 | a0001 | c0004 | t0001 | g0089 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02055 | hp2 | a0001 | c0005 | t0019 | g0388 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02056 | hp1 | a0001 | c0003 | t0002 | g0266 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02056 | hp2 | a0002 | c0002 | t0007 | g0035 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0076 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02071 | hp2 | a0001 | c0005 | t0004 | g0202 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02074 | hp1 | a0001 | c0004 | t0002 | g0326 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0078 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02080 | hp1 | a0001 | c0004 | t0001 | g0080 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02080 | hp2 | a0002 | c0002 | t0009 | g0304 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02083 | hp1 | a0001 | c0004 | t0001 | g0171 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02083 | hp2 | a0002 | c0002 | t0003 | g0249 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0250 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0098 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02132 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0085 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02135 | hp1 | a0002 | c0002 | t0003 | g0133 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0168 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02145 | hp1 | a0001 | c0005 | t0011 | g0298 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02145 | hp2 | a0001 | c0009 | t0006 | g0384 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02148 | hp1 | a0001 | c0003 | t0002 | g0272 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02148 | hp2 | a0002 | c0002 | t0003 | g0135 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02155 | hp1 | a0001 | c0005 | t0004 | g0157 | EAS | CDX | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02155 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | CDX | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | CDX | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02165 | hp2 | a0002 | c0002 | t0003 | g0144 | EAS | CDX | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0379 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02257 | hp2 | a0001 | c0005 | t0015 | g0321 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02258 | hp1 | a0001 | c0005 | t0027 | g0270 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02258 | hp2 | a0001 | c0012 | t0002 | g0261 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02280 | hp1 | a0001 | c0005 | t0004 | g0193 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0189 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02451 | hp1 | a0001 | c0004 | t0006 | g0382 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02523 | hp1 | a0001 | c0004 | t0001 | g0074 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02523 | hp2 | a0002 | c0002 | t0003 | g0142 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0188 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02602 | hp1 | a0001 | c0001 | t0010 | g0049 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02602 | hp2 | a0002 | c0002 | t0003 | g0115 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02615 | hp1 | a0001 | c0005 | t0011 | g0277 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02615 | hp2 | a0001 | c0005 | t0004 | g0198 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0323 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02622 | hp2 | a0001 | c0009 | t0001 | g0172 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0206 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02647 | hp1 | a0001 | c0004 | t0002 | g0285 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02647 | hp2 | a0001 | c0005 | t0004 | g0201 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02683 | hp1 | a0002 | c0002 | t0003 | g0055 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02683 | hp2 | a0001 | c0004 | t0001 | g0108 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02717 | hp1 | a0001 | c0005 | t0004 | g0237 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0320 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02723 | hp1 | a0001 | c0003 | t0002 | g0284 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02723 | hp2 | a0001 | c0005 | t0004 | g0177 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02735 | hp1 | a0001 | c0003 | t0002 | g0273 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02735 | hp2 | a0002 | c0008 | t0001 | g0216 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0381 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02738 | hp2 | a0002 | c0002 | t0003 | g0162 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0352 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0374 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02886 | hp1 | a0001 | c0003 | t0026 | g0353 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0337 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02895 | hp1 | a0001 | c0005 | t0004 | g0151 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02895 | hp2 | a0001 | c0004 | t0002 | g0013 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02896 | hp1 | a0002 | c0015 | t0001 | g0009 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02897 | hp1 | a0002 | c0015 | t0001 | g0009 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02897 | hp2 | a0001 | c0004 | t0002 | g0013 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0340 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02922 | hp2 | a0001 | c0005 | t0004 | g0238 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02965 | hp1 | a0005 | c0010 | t0002 | g0257 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02965 | hp2 | a0001 | c0005 | t0029 | g0370 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02970 | hp1 | a0001 | c0005 | t0017 | g0369 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0322 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0190 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02976 | hp2 | a0001 | c0017 | t0001 | g0220 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03017 | hp1 | a0001 | c0003 | t0002 | g0317 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03017 | hp2 | a0002 | c0002 | t0009 | g0259 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03041 | hp1 | a0001 | c0005 | t0004 | g0196 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0376 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0324 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0185 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0137 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03139 | hp1 | a0001 | c0005 | t0004 | g0113 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0260 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0207 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03209 | hp1 | a0001 | c0005 | t0004 | g0195 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0305 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03225 | hp1 | a0001 | c0005 | t0015 | g0366 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0359 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03239 | hp1 | a0003 | c0006 | t0002 | g0014 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03239 | hp2 | a0003 | c0006 | t0001 | g0232 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03453 | hp1 | a0001 | c0005 | t0019 | g0383 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03486 | hp2 | a0001 | c0005 | t0011 | g0254 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0313 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03490 | hp2 | a0002 | c0002 | t0003 | g0058 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03491 | hp1 | a0001 | c0001 | t0018 | g0372 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0330 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03492 | hp1 | a0001 | c0001 | t0018 | g0373 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03492 | hp2 | a0002 | c0002 | t0003 | g0057 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0386 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03516 | hp2 | a0001 | c0005 | t0004 | g0240 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0245 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03540 | hp2 | a0001 | c0021 | t0002 | g0271 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03579 | hp1 | a0001 | c0004 | t0006 | g0375 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03579 | hp2 | a0005 | c0010 | t0002 | g0256 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03669 | hp1 | a0001 | c0004 | t0001 | g0176 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0389 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0139 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03704 | hp2 | a0001 | c0004 | t0001 | g0077 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0242 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03710 | hp2 | a0002 | c0002 | t0022 | g0021 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0385 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0348 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03927 | hp1 | a0001 | c0005 | t0016 | g0310 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0212 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0312 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03942 | hp2 | a0001 | c0004 | t0001 | g0215 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG04115 | hp1 | a0001 | c0001 | t0021 | g0020 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG04115 | hp2 | a0001 | c0004 | t0001 | g0179 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0209 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG04184 | hp2 | a0001 | c0004 | t0002 | g0347 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0210 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG04199 | hp2 | a0002 | c0002 | t0009 | g0255 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG04204 | hp1 | a0002 | c0008 | t0001 | g0214 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0274 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0218 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18612 | hp1 | a0002 | c0002 | t0007 | g0036 | EAS | CHB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18612 | hp2 | a0001 | c0003 | t0002 | g0357 | EAS | CHB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18747 | hp1 | a0002 | c0002 | t0003 | g0053 | EAS | CHB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18747 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | CHB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18906 | hp1 | a0001 | c0009 | t0002 | g0367 | AFR | YRI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18906 | hp2 | a0002 | c0007 | t0001 | g0197 | AFR | YRI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0016 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18940 | hp2 | a0002 | c0002 | t0003 | g0100 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0327 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18941 | hp2 | a0002 | c0002 | t0003 | g0094 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18943 | hp1 | a0001 | c0005 | t0005 | g0032 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18943 | hp2 | a0001 | c0003 | t0002 | g0291 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18944 | hp1 | a0002 | c0002 | t0009 | g0301 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18944 | hp2 | a0002 | c0007 | t0002 | g0333 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18945 | hp1 | a0002 | c0002 | t0003 | g0068 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18945 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18946 | hp1 | a0003 | c0006 | t0001 | g0224 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18946 | hp2 | a0003 | c0014 | t0002 | g0319 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18947 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18947 | hp2 | a0001 | c0003 | t0002 | g0309 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18949 | hp1 | a0001 | c0004 | t0001 | g0211 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18949 | hp2 | a0001 | c0005 | t0004 | g0165 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18950 | hp1 | a0003 | c0006 | t0001 | g0062 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18950 | hp2 | a0001 | c0005 | t0005 | g0033 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18951 | hp1 | a0001 | c0005 | t0008 | g0079 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18951 | hp2 | a0002 | c0002 | t0003 | g0101 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18952 | hp1 | a0001 | c0003 | t0002 | g0311 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18952 | hp2 | a0002 | c0002 | t0003 | g0158 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18954 | hp1 | a0002 | c0007 | t0002 | g0017 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18954 | hp2 | a0002 | c0008 | t0001 | g0174 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18957 | hp1 | a0002 | c0002 | t0003 | g0096 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18957 | hp2 | a0002 | c0002 | t0005 | g0048 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18959 | hp1 | a0003 | c0006 | t0012 | g0088 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18959 | hp2 | a0001 | c0003 | t0001 | g0243 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18960 | hp1 | a0001 | c0004 | t0024 | g0072 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18960 | hp2 | a0001 | c0004 | t0004 | g0175 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18962 | hp1 | a0001 | c0005 | t0008 | g0064 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18962 | hp2 | a0002 | c0002 | t0003 | g0120 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18964 | hp1 | a0001 | c0004 | t0001 | g0217 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18964 | hp2 | a0001 | c0004 | t0001 | g0011 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0329 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18966 | hp2 | a0003 | c0013 | t0001 | g0227 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18967 | hp1 | a0002 | c0002 | t0003 | g0112 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18967 | hp2 | a0002 | c0002 | t0003 | g0093 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18968 | hp1 | a0001 | c0003 | t0002 | g0362 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18968 | hp2 | a0001 | c0004 | t0001 | g0081 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18969 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18969 | hp2 | a0002 | c0007 | t0002 | g0334 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18970 | hp1 | a0003 | c0006 | t0012 | g0159 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18970 | hp2 | a0002 | c0002 | t0025 | g0251 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18971 | hp1 | a0002 | c0007 | t0002 | g0017 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18971 | hp2 | a0002 | c0002 | t0003 | g0059 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18975 | hp2 | a0001 | c0005 | t0005 | g0044 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18979 | hp1 | a0001 | c0003 | t0002 | g0262 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18979 | hp2 | a0001 | c0004 | t0001 | g0170 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18980 | hp1 | a0002 | c0002 | t0007 | g0030 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18980 | hp2 | a0001 | c0003 | t0002 | g0308 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18981 | hp1 | a0002 | c0002 | t0003 | g0103 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18981 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18983 | hp1 | a0002 | c0002 | t0003 | g0236 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18984 | hp1 | a0002 | c0002 | t0009 | g0287 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18984 | hp2 | a0001 | c0019 | t0001 | g0073 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18985 | hp1 | a0001 | c0003 | t0002 | g0015 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18985 | hp2 | a0002 | c0002 | t0007 | g0026 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18989 | hp1 | a0001 | c0004 | t0001 | g0213 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18989 | hp2 | a0002 | c0002 | t0009 | g0263 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18990 | hp1 | a0001 | c0005 | t0005 | g0029 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18990 | hp2 | a0001 | c0004 | t0013 | g0052 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18993 | hp1 | a0001 | c0003 | t0002 | g0015 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18993 | hp2 | a0001 | c0005 | t0005 | g0041 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18994 | hp1 | a0002 | c0002 | t0003 | g0105 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18994 | hp2 | a0001 | c0005 | t0005 | g0042 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18995 | hp1 | a0003 | c0006 | t0001 | g0230 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18995 | hp2 | a0001 | c0018 | t0028 | g0325 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18997 | hp1 | a0006 | c0016 | t0003 | g0063 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18997 | hp2 | a0001 | c0005 | t0005 | g0027 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0069 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18998 | hp2 | a0002 | c0002 | t0003 | g0166 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18999 | hp1 | a0001 | c0004 | t0001 | g0164 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0241 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19000 | hp1 | a0002 | c0002 | t0003 | g0161 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19000 | hp2 | a0001 | c0003 | t0010 | g0028 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19002 | hp1 | a0001 | c0003 | t0002 | g0316 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19002 | hp2 | a0001 | c0005 | t0004 | g0130 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19004 | hp2 | a0003 | c0013 | t0001 | g0228 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0065 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19007 | hp1 | a0002 | c0002 | t0003 | g0066 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19007 | hp2 | a0001 | c0003 | t0002 | g0361 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19009 | hp1 | a0002 | c0002 | t0003 | g0084 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19009 | hp2 | a0001 | c0005 | t0008 | g0156 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19011 | hp1 | a0001 | c0003 | t0002 | g0289 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19011 | hp2 | a0002 | c0002 | t0003 | g0087 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19012 | hp1 | a0001 | c0004 | t0010 | g0034 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19012 | hp2 | a0001 | c0003 | t0002 | g0300 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19030 | hp1 | a0001 | c0012 | t0001 | g0116 | AFR | LWK | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19030 | hp2 | a0001 | c0005 | t0006 | g0380 | AFR | LWK | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19043 | hp1 | a0001 | c0005 | t0011 | g0278 | AFR | LWK | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19043 | hp2 | a0001 | c0005 | t0031 | g0377 | AFR | LWK | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19054 | hp1 | a0001 | c0005 | t0004 | g0114 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19054 | hp2 | a0001 | c0004 | t0001 | g0178 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19055 | hp1 | a0002 | c0002 | t0003 | g0067 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19055 | hp2 | a0001 | c0005 | t0004 | g0129 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19056 | hp1 | a0002 | c0002 | t0003 | g0104 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | g0328 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19057 | hp2 | a0001 | c0005 | t0004 | g0131 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19060 | hp1 | a0001 | c0004 | t0001 | g0011 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19060 | hp2 | a0003 | c0006 | t0001 | g0226 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19063 | hp2 | a0001 | c0004 | t0001 | g0235 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19064 | hp1 | a0003 | c0006 | t0001 | g0229 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19064 | hp2 | a0003 | c0014 | t0002 | g0307 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19065 | hp1 | a0002 | c0002 | t0009 | g0360 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19065 | hp2 | a0001 | c0003 | t0002 | g0292 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19068 | hp1 | a0002 | c0002 | t0007 | g0025 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19068 | hp2 | a0003 | c0006 | t0001 | g0225 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0060 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19070 | hp2 | a0001 | c0003 | t0002 | g0342 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0267 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19074 | hp2 | a0003 | c0006 | t0001 | g0223 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19077 | hp2 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19079 | hp1 | a0002 | c0002 | t0007 | g0022 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19079 | hp2 | a0002 | c0002 | t0003 | g0092 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19080 | hp1 | a0001 | c0003 | t0002 | g0293 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19080 | hp2 | a0002 | c0002 | t0007 | g0024 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0132 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19081 | hp2 | a0002 | c0002 | t0007 | g0031 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19082 | hp1 | a0001 | c0005 | t0005 | g0023 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19082 | hp2 | a0002 | c0002 | t0003 | g0152 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19083 | hp1 | a0002 | c0002 | t0007 | g0037 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19083 | hp2 | a0002 | c0002 | t0009 | g0295 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19084 | hp1 | a0001 | c0003 | t0002 | g0314 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19084 | hp2 | a0001 | c0004 | t0013 | g0051 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19085 | hp1 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19085 | hp2 | a0001 | c0003 | t0002 | g0252 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0016 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19087 | hp2 | a0003 | c0006 | t0012 | g0173 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19088 | hp1 | a0001 | c0005 | t0005 | g0047 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0095 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19090 | hp1 | a0001 | c0004 | t0001 | g0082 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19090 | hp2 | a0001 | c0003 | t0002 | g0290 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0102 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19091 | hp2 | a0002 | c0002 | t0007 | g0046 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19240 | hp1 | a0001 | c0005 | t0004 | g0192 | AFR | YRI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0205 | AFR | YRI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0160 | AFR | ASW | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA20129 | hp2 | a0001 | c0004 | t0002 | g0258 | AFR | ASW | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0279 | EUR | TSI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA20805 | hp1 | a0002 | c0002 | t0003 | g0203 | EUR | TSI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA20805 | hp2 | a0001 | c0004 | t0001 | g0056 | EUR | TSI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA20905 | hp1 | a0001 | c0001 | t0010 | g0038 | SAS | GIH | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0071 | SAS | GIH | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0117 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0351 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02109 | hp1 | a0002 | c0002 | t0003 | g0155 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0339 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02486 | hp1 | a0001 | c0004 | t0001 | g0147 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02486 | hp2 | a0001 | c0005 | t0017 | g0371 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0341 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03471 | hp1 | a0001 | c0004 | t0030 | g0368 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG06807 | hp1 | a0001 | c0003 | t0006 | g0387 | AFR | USA | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| HG06807 | hp2 | a0001 | c0005 | t0023 | g0239 | AFR | USA | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0344 | AFR | USA | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0075 | AFR | USA | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA21309 | hp1 | a0002 | c0002 | t0020 | g0019 | AFR | LWK | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0281 | REF | REF | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0181 | REF | REF | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180313827
|
T | C | 3 | a0002a0004a0006 | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
missense_variant | MODERATE | c.1411A>G | p.Ile471Val | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/19 | 1530/3034 | 1411/2049 | 471/682 | chr5 | 180313827 | ||
| chr5:180313875
|
T | G | 1 | a0003 | 18 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(15): Show |
missense_variant | MODERATE | c.1363A>C | p.Ile455Leu | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/19 | 1482/3034 | 1363/2049 | 455/682 | chr5 | 180313875 | ||
| chr5:180316385
|
G | T | 1 | a0004 | 2 | HG01261.hp1 HG01496.hp2 |
missense_variant | MODERATE | c.1229C>A | p.Thr410Lys | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/19 | 1348/3034 | 1229/2049 | 410/682 | chr5 | 180316385 | ||
| chr5:180316994
|
CATAGTAT others(3): Show |
C | 1 | a0006 | 1 | NA18997.hp1 | frameshift_variant | HIGH | c.1013_1022delTCAATA others(4): Show |
p.Phe338fs | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 11/19 | 1141/3034 | 1013/2049 | 338/682 | chr5 | 180316994 | ||
| chr5:180318901
|
C | T | 1 | a0005 | 2 | HG02965.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.850G>A | p.Ala284Thr | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/19 | 969/3034 | 850/2049 | 284/682 | chr5 | 180318901 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180302429
|
T | A | 1 | a0001c0019 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.1998A>T | p.Gly666Gly | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/19 | 2117/3034 | 1998/2049 | 666/682 | chr5 | 180302429 | ||
| chr5:180302519
|
A | G | 16 | a0001c0003a0001c0004a0001c0005others(13): Show | 311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
synonymous_variant | LOW | c.1908T>C | p.Ile636Ile | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/19 | 2027/3034 | 1908/2049 | 636/682 | chr5 | 180302519 | ||
| chr5:180307200
|
A | G | 9 | a0001c0004a0001c0012a0001c0018others(6): Show | 86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
synonymous_variant | LOW | c.1650T>C | p.Tyr550Tyr | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/19 | 1769/3034 | 1650/2049 | 550/682 | chr5 | 180307200 | ||
| chr5:180307230
|
C | G | 3 | a0001c0018a0003c0006a0003c0013 | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
synonymous_variant | LOW | c.1620G>C | p.Ser540Ser | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/19 | 1739/3034 | 1620/2049 | 540/682 | chr5 | 180307230 | ||
| chr5:180313954
|
C | T | 1 | a0001c0017 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1284G>A | p.Ala428Ala | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/19 | 1403/3034 | 1284/2049 | 428/682 | chr5 | 180313954 | ||
| chr5:180317009
|
T | G | 4 | a0001c0003a0002c0020a0003c0013others(1): Show | 77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
synonymous_variant | LOW | c.1008A>C | p.Ser336Ser | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 11/19 | 1127/3034 | 1008/2049 | 336/682 | chr5 | 180317009 | ||
| chr5:180318854
|
G | A | 2 | a0001c0009a0001c0021 | 4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
synonymous_variant | LOW | c.897C>T | p.Ala299Ala | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/19 | 1016/3034 | 897/2049 | 299/682 | chr5 | 180318854 | ||
| chr5:180338506
|
G | A | 1 | a0002c0015 | 2 | HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.102C>T | p.Gly34Gly | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/19 | 221/3034 | 102/2049 | 34/682 | chr5 | 180338506 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180300706
|
A | G | 6 | a0001c0003t0008a0001c0005t0005a0001c0005t0008others(3): Show | 24 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*858T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 858 | chr5 | 180300706 | |||||
| chr5:180300804
|
A | C | 5 | a0001c0004t0004a0001c0005t0004a0001c0005t0011others(2): Show | 28 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*760T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 760 | chr5 | 180300804 | |||||
| chr5:180300872
|
G | A | 1 | a0001c0005t0027 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*692C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 692 | chr5 | 180300872 | |||||
| chr5:180300957
|
C | T | 9 | a0001c0005t0003a0002c0002t0003a0002c0002t0007others(6): Show | 88 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*607G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 607 | chr5 | 180300957 | |||||
| chr5:180300975
|
T | C | 1 | a0001c0004t0024 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*589A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 589 | chr5 | 180300975 | |||||
| chr5:180300988
|
G | A | 6 | a0001c0003t0008a0001c0005t0005a0001c0005t0008others(3): Show | 24 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*576C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 576 | chr5 | 180300988 | |||||
| chr5:180301000
|
G | A | 2 | a0001c0018t0028a0003c0006t0012 | 4 | NA18959.hp1 NA18970.hp1 NA18995.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*564C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 564 | chr5 | 180301000 | |||||
| chr5:180301010
|
G | T | 1 | a0001c0004t0024 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*554C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 554 | chr5 | 180301010 | |||||
| chr5:180301328
|
C | G | 5 | a0001c0005t0015a0001c0005t0017a0001c0005t0023others(2): Show | 7 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*236G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 236 | chr5 | 180301328 | |||||
| chr5:180301368
|
C | T | 1 | a0001c0003t0026 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*196G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 196 | chr5 | 180301368 | |||||
| chr5:180301552
|
A | G | 1 | a0001c0001t0014 | 2 | HG03195.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 12 | chr5 | 180301552 | |||||
| chr5:180353263
|
G | A | 1 | a0002c0002t0025 | 1 | NA18970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | chr5 | 180353263 | ||||||
| chr5:180353274
|
G | GGGGCTCC others(5): Show |
1 | a0001c0004t0013 | 2 | NA18990.hp2 NA19084.hp2 |
5_prime_UTR_variant | MODIFIER | c.-69_-58dupACGGAGGA others(4): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 58 | chr5 | 180353274 | |||||
| chr5:180353280
|
CCTCCGTG others(14): Show |
C | 3 | a0001c0004t0030a0001c0005t0017a0001c0005t0029 | 4 | HG02486.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-84_-64delCCCACGGA others(13): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 64 | chr5 | 180353280 | |||||
| chr5:180353292
|
CCTCCGTG others(2): Show |
C | 28 | a0001c0001t0002a0001c0001t0006a0001c0001t0014others(25): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
5_prime_UTR_variant | MODIFIER | c.-84_-76delCCCACGGA others(1): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 76 | chr5 | 180353292 | |||||
| chr5:180353296
|
C | T | 6 | a0001c0001t0010a0001c0003t0010a0001c0004t0010others(3): Show | 29 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-79G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 79 | chr5 | 180353296 | |||||
| chr5:180353305
|
C | T | 1 | a0002c0002t0022 | 1 | HG03710.hp2 | 5_prime_UTR_variant | MODIFIER | c.-88G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 88 | chr5 | 180353305 | |||||
| chr5:180353307
|
TGGGCTCC others(11): Show |
T | 1 | a0002c0002t0020 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-108_-91delGCGGAGC others(11): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 91 | chr5 | 180353307 | |||||
| chr5:180353310
|
G | T | 1 | a0001c0001t0021 | 1 | HG04115.hp1 | 5_prime_UTR_variant | MODIFIER | c.-93C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 93 | chr5 | 180353310 | |||||
| chr5:180353328
|
G | A | 8 | a0001c0001t0006a0001c0001t0018a0001c0003t0006others(5): Show | 19 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-111C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 111 | chr5 | 180353328 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180301707
|
T | C | 167 | a0001c0003t0001g0189a0001c0003t0001g0242a0001c0003t0002g0292others(164): Show | 175 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.2005-99A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180301707 | ||||||
| chr5:180301849
|
T | C | 74 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(71): Show | 79 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.2005-241A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180301849 | ||||||
| chr5:180301860
|
A | C | 166 | a0001c0003t0001g0242a0001c0003t0002g0292a0001c0003t0008g0145others(163): Show | 174 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.2005-252T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180301860 | ||||||
| chr5:180301930
|
T | C | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.2005-322A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180301930 | ||||||
| chr5:180301936
|
T | C | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.2005-328A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180301936 | ||||||
| chr5:180301998
|
C | G | 114 | a0001c0003t0008g0145a0001c0005t0003g0107a0001c0005t0003g0134others(111): Show | 119 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.2005-390G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180301998 | ||||||
| chr5:180302009
|
G | A | 126 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(123): Show | 134 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.2005-401C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302009 | ||||||
| chr5:180302018
|
C | CGGTGGCT others(1694): Show |
1 | a0001c0003t0002g0266 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2004+404_2004+405i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302018 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1693): Show |
1 | a0001c0005t0008g0079 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1702): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
1 | a0002c0002t0003g0053 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
18 | a0001c0003t0008g0145a0001c0005t0005g0023a0001c0005t0005g0027others(15): Show | 18 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
82 | a0001c0005t0003g0107a0001c0005t0003g0134a0002c0002t0003g0002others(79): Show | 87 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1693): Show |
2 | a0001c0005t0005g0041a0001c0005t0005g0047 | 2 | NA18993.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1702): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
7 | a0001c0005t0015g0321a0001c0005t0015g0366a0001c0005t0017g0369others(4): Show | 7 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
1 | a0002c0002t0025g0251 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1695): Show |
1 | a0002c0002t0007g0035 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1704): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1691): Show |
1 | a0001c0005t0005g0029 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1700): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
1 | a0001c0003t0006g0387 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
1 | a0001c0005t0006g0380 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
1 | a0001c0004t0013g0052 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
3 | a0001c0004t0030g0368a0005c0010t0002g0256a0005c0010t0002g0257 | 3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1693): Show |
2 | a0001c0004t0001g0212a0001c0004t0001g0215 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1702): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
46 | a0001c0003t0002g0292a0001c0004t0001g0004a0001c0004t0001g0010others(43): Show | 49 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1693): Show |
1 | a0001c0003t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1702): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
1 | a0001c0003t0002g0362 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
1 | a0001c0003t0002g0352 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
1 | a0003c0014t0002g0307 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
60 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(57): Show | 65 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
1 | a0001c0003t0001g0231 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
1 | a0001c0003t0026g0353 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1695): Show |
1 | a0001c0003t0002g0272 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1704): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302029
|
A | ACCTGTAA others(1694): Show |
4 | a0001c0005t0002g0358a0001c0009t0001g0172a0001c0009t0002g0367others(1): Show | 4 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | ||||||
| chr5:180302062
|
A | G | 239 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(236): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.2004+361T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302062 | ||||||
| chr5:180302085
|
A | T | 3 | a0001c0001t0006g0378a0001c0001t0006g0381a0001c0001t0006g0385 | 3 | HG02015.hp1 HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2004+338T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302085 | ||||||
| chr5:180302104
|
G | A | 5 | a0001c0005t0002g0358a0001c0009t0001g0172a0001c0009t0002g0367others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004+319C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302104 | ||||||
| chr5:180302115
|
G | A | 5 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0001g0245others(2): Show | 5 | HG02630.hp1 HG02647.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2004+308C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302115 | ||||||
| chr5:180302167
|
G | A | 3 | a0001c0005t0011g0298a0002c0002t0008g0012a0002c0002t0008g0248 | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+256C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302167 | ||||||
| chr5:180302201
|
C | T | 5 | a0001c0005t0004g0113a0001c0005t0004g0237a0001c0005t0004g0238others(2): Show | 5 | HG02717.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2004+222G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302201 | ||||||
| chr5:180302283
|
T | A | 75 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(72): Show | 80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.2004+140A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302283 | ||||||
| chr5:180302286
|
CA | C | 7 | a0001c0001t0001g0125a0001c0003t0002g0318a0001c0004t0001g0215others(4): Show | 7 | HG00558.hp2 HG01517.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004+136delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302286 | ||||||
| chr5:180302286
|
CAA | C | 113 | a0001c0003t0008g0145a0001c0005t0003g0107a0001c0005t0003g0134others(110): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.2004+135_2004+136d others(4): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302286 | ||||||
| chr5:180302328
|
C | T | 240 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(237): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.2004+95G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302328 | ||||||
| chr5:180302391
|
T | C | 15 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(12): Show | 16 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(13): Show |
intron_variant | MODIFIER | c.2004+32A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302391 | ||||||
| chr5:180302625
|
A | G | 114 | a0001c0003t0008g0145a0001c0005t0003g0107a0001c0005t0003g0134others(111): Show | 119 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1843-41T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180302625 | ||||||
| chr5:180302853
|
G | A | 1 | a0001c0005t0011g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1843-269C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180302853 | ||||||
| chr5:180302967
|
C | T | 69 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(66): Show | 74 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1843-383G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180302967 | ||||||
| chr5:180303004
|
T | C | 298 | a0001c0001t0018g0372a0001c0001t0018g0373a0001c0003t0001g0065others(295): Show | 313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1843-420A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303004 | ||||||
| chr5:180303045
|
T | C | 72 | a0001c0001t0006g0389a0001c0001t0006g0390a0001c0003t0008g0145others(69): Show | 75 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1843-461A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303045 | ||||||
| chr5:180303056
|
T | C | 52 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(49): Show | 55 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1843-472A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303056 | ||||||
| chr5:180303065
|
TA | T | 51 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(48): Show | 54 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1843-482delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303065 | ||||||
| chr5:180303082
|
T | G | 50 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(47): Show | 53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1843-498A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303082 | ||||||
| chr5:180303090
|
T | C | 58 | a0001c0001t0021g0020a0001c0004t0001g0004a0001c0004t0001g0010others(55): Show | 61 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1843-506A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303090 | ||||||
| chr5:180303092
|
T | C | 50 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(47): Show | 53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1843-508A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303092 | ||||||
| chr5:180303102
|
G | C | 87 | a0001c0001t0006g0386a0001c0003t0001g0168a0001c0003t0008g0145others(84): Show | 90 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1843-518C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303102 | ||||||
| chr5:180303103
|
G | A | 1 | a0001c0001t0006g0386 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1843-519C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303103 | ||||||
| chr5:180303122
|
G | C | 77 | a0001c0003t0008g0145a0001c0004t0001g0004a0001c0004t0001g0010others(74): Show | 80 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1843-538C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303122 | ||||||
| chr5:180303184
|
G | T | 186 | a0001c0003t0008g0145a0001c0004t0001g0004a0001c0004t0001g0010others(183): Show | 194 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.1843-600C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303184 | ||||||
| chr5:180303217
|
C | G | 27 | a0001c0005t0004g0113a0001c0005t0004g0114a0001c0005t0004g0129others(24): Show | 27 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1843-633G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303217 | ||||||
| chr5:180303220
|
A | G | 2 | a0001c0001t0006g0374a0001c0001t0006g0376 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1843-636T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303220 | ||||||
| chr5:180303221
|
C | T | 20 | a0001c0003t0008g0145a0001c0005t0005g0023a0001c0005t0005g0027others(17): Show | 20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-637G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303221 | ||||||
| chr5:180303224
|
C | A | 27 | a0001c0005t0004g0113a0001c0005t0004g0114a0001c0005t0004g0129others(24): Show | 27 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1843-640G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303224 | ||||||
| chr5:180303225
|
G | A | 28 | a0001c0001t0002g0355a0001c0005t0004g0113a0001c0005t0004g0114others(25): Show | 28 | HG01167.hp2 HG01358.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1843-641C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303225 | ||||||
| chr5:180303228
|
A | T | 27 | a0001c0005t0004g0113a0001c0005t0004g0114a0001c0005t0004g0129others(24): Show | 27 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1843-644T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303228 | ||||||
| chr5:180303229
|
CA | C | 184 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(181): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1843-646delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303229 | ||||||
| chr5:180303232
|
A | C | 2 | a0001c0004t0001g0187a0001c0004t0002g0013 | 3 | HG01952.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1843-648T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303232 | ||||||
| chr5:180303234
|
A | C | 2 | a0001c0004t0001g0187a0001c0004t0002g0013 | 3 | HG01952.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1843-650T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303234 | ||||||
| chr5:180303236
|
A | C | 1 | a0001c0004t0002g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1843-652T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303236 | ||||||
| chr5:180303380
|
G | A | 1 | a0002c0002t0003g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1843-796C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303380 | ||||||
| chr5:180303426
|
G | A | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1843-842C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303426 | ||||||
| chr5:180303432
|
G | T | 2 | a0002c0002t0008g0012a0002c0002t0008g0248 | 3 | HG01099.hp1 HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1843-848C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303432 | ||||||
| chr5:180303460
|
A | C | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(44): Show | 50 | HG00280.hp1 HG01255.hp1 HG01258.hp1 others(47): Show |
intron_variant | MODIFIER | c.1843-876T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303460 | ||||||
| chr5:180303478
|
A | G | 48 | a0001c0001t0002g0355a0001c0004t0001g0004a0001c0004t0001g0010others(45): Show | 51 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1843-894T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303478 | ||||||
| chr5:180303700
|
C | G | 1 | a0001c0003t0002g0328 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1842+1072G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303700 | ||||||
| chr5:180303843
|
A | G | 241 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(238): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1842+929T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303843 | ||||||
| chr5:180303938
|
T | C | 117 | a0001c0003t0008g0145a0001c0004t0030g0368a0001c0005t0003g0107others(114): Show | 122 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1842+834A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303938 | ||||||
| chr5:180304014
|
T | C | 241 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(238): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1842+758A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304014 | ||||||
| chr5:180304053
|
A | C | 1 | a0001c0001t0002g0341 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1842+719T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304053 | ||||||
| chr5:180304113
|
G | A | 87 | a0001c0005t0003g0107a0001c0005t0003g0134a0002c0002t0003g0002others(84): Show | 92 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1842+659C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304113 | ||||||
| chr5:180304135
|
G | A | 1 | a0001c0003t0002g0292 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1842+637C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304135 | ||||||
| chr5:180304297
|
G | T | 87 | a0001c0005t0003g0107a0001c0005t0003g0134a0002c0002t0003g0002others(84): Show | 92 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1842+475C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304297 | ||||||
| chr5:180304328
|
T | G | 87 | a0001c0005t0003g0107a0001c0005t0003g0134a0002c0002t0003g0002others(84): Show | 92 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1842+444A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304328 | ||||||
| chr5:180304363
|
C | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0169a0001c0001t0002g0359 | 3 | HG02818.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1842+409G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304363 | ||||||
| chr5:180304377
|
G | A | 239 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(236): Show | 252 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.1842+395C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304377 | ||||||
| chr5:180304412
|
A | G | 1 | a0001c0005t0006g0380 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1842+360T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304412 | ||||||
| chr5:180304433
|
G | A | 1 | a0001c0005t0004g0130 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1842+339C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304433 | ||||||
| chr5:180304466
|
C | A | 127 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(124): Show | 135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1842+306G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304466 | ||||||
| chr5:180304575
|
G | T | 1 | a0001c0004t0001g0056 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1842+197C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304575 | ||||||
| chr5:180304635
|
C | G | 241 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(238): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1842+137G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304635 | ||||||
| chr5:180304695
|
C | T | 127 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(124): Show | 135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1842+77G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304695 | ||||||
| chr5:180304715
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1842+57C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304715 | ||||||
| chr5:180305126
|
C | T | 2 | a0002c0002t0003g0068a0002c0002t0003g0069 | 2 | NA18945.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1675-187G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305126 | ||||||
| chr5:180305221
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1675-282C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305221 | ||||||
| chr5:180305240
|
C | A | 114 | a0001c0003t0008g0145a0001c0005t0003g0107a0001c0005t0003g0134others(111): Show | 119 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1675-301G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305240 | ||||||
| chr5:180305350
|
A | G | 268 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(265): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.1675-411T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305350 | ||||||
| chr5:180305426
|
T | C | 1 | a0001c0003t0002g0320 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1675-487A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305426 | ||||||
| chr5:180305441
|
C | T | 1 | a0001c0004t0002g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1675-502G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305441 | ||||||
| chr5:180305447
|
G | A | 1 | a0001c0012t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1675-508C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305447 | ||||||
| chr5:180305604
|
C | T | 1 | a0001c0005t0011g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1675-665G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305604 | ||||||
| chr5:180305655
|
C | T | 1 | a0001c0005t0011g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1675-716G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305655 | ||||||
| chr5:180305678
|
T | G | 241 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(238): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1675-739A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305678 | ||||||
| chr5:180305680
|
C | A | 19 | a0001c0003t0008g0145a0001c0005t0005g0023a0001c0005t0005g0027others(16): Show | 19 | HG00609.hp1 HG00673.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1675-741G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305680 | ||||||
| chr5:180305680
|
C | T | 50 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(47): Show | 53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1675-741G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305680 | ||||||
| chr5:180305741
|
C | T | 17 | a0001c0005t0005g0023a0001c0005t0005g0027a0001c0005t0005g0029others(14): Show | 17 | HG00609.hp1 HG00673.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.1675-802G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305741 | ||||||
| chr5:180305771
|
A | G | 128 | a0001c0001t0002g0344a0001c0003t0001g0065a0001c0003t0001g0078others(125): Show | 136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1675-832T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305771 | ||||||
| chr5:180305797
|
C | T | 127 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(124): Show | 135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1675-858G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305797 | ||||||
| chr5:180305974
|
T | G | 114 | a0001c0003t0008g0145a0001c0005t0003g0107a0001c0005t0003g0134others(111): Show | 119 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1675-1035A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305974 | ||||||
| chr5:180305983
|
CT | C | 218 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(215): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1675-1045delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305983 | ||||||
| chr5:180305986
|
T | C | 3 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0001g0245 | 3 | HG02630.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1675-1047A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305986 | ||||||
| chr5:180305987
|
T | C | 1 | a0002c0008t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1675-1048A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305987 | ||||||
| chr5:180306016
|
G | A | 1 | a0001c0005t0011g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1675-1077C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306016 | ||||||
| chr5:180306193
|
C | T | 1 | a0002c0008t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1674+983G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306193 | ||||||
| chr5:180306372
|
G | A | 1 | a0002c0008t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1674+804C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306372 | ||||||
| chr5:180306407
|
C | T | 270 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(267): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.1674+769G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306407 | ||||||
| chr5:180306413
|
G | T | 7 | a0001c0005t0015g0321a0001c0005t0015g0366a0001c0005t0017g0369others(4): Show | 7 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+763C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306413 | ||||||
| chr5:180306440
|
T | C | 270 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(267): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.1674+736A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306440 | ||||||
| chr5:180306447
|
A | G | 20 | a0001c0003t0008g0145a0001c0005t0005g0023a0001c0005t0005g0027others(17): Show | 20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1674+729T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306447 | ||||||
| chr5:180306466
|
C | T | 2 | a0001c0004t0001g0187a0001c0004t0002g0013 | 3 | HG01952.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1674+710G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306466 | ||||||
| chr5:180306481
|
T | C | 1 | a0001c0004t0001g0180 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1674+695A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306481 | ||||||
| chr5:180306515
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1674+661C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306515 | ||||||
| chr5:180306551
|
C | T | 1 | a0001c0001t0002g0336 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1674+625G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306551 | ||||||
| chr5:180306691
|
C | T | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1674+485G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306691 | ||||||
| chr5:180306707
|
C | A | 17 | a0001c0005t0005g0023a0001c0005t0005g0027a0001c0005t0005g0029others(14): Show | 17 | HG00609.hp1 HG00673.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.1674+469G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306707 | ||||||
| chr5:180306727
|
G | A | 1 | a0001c0009t0006g0384 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1674+449C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306727 | ||||||
| chr5:180306735
|
C | G | 1 | a0001c0005t0011g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1674+441G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306735 | ||||||
| chr5:180306789
|
G | C | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1674+387C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306789 | ||||||
| chr5:180306865
|
T | G | 1 | a0001c0005t0015g0366 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1674+311A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306865 | ||||||
| chr5:180306916
|
C | T | 7 | a0001c0005t0015g0321a0001c0005t0015g0366a0001c0005t0017g0369others(4): Show | 7 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+260G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306916 | ||||||
| chr5:180306928
|
G | A | 7 | a0001c0004t0001g0211a0001c0004t0001g0212a0001c0004t0001g0213others(4): Show | 7 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+248C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306928 | ||||||
| chr5:180306934
|
T | C | 270 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(267): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.1674+242A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306934 | ||||||
| chr5:180306943
|
C | T | 1 | a0002c0002t0008g0248 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1674+233G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306943 | ||||||
| chr5:180306961
|
T | A | 3 | a0001c0004t0030g0368a0005c0010t0002g0256a0005c0010t0002g0257 | 3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1674+215A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306961 | ||||||
| chr5:180307037
|
C | T | 7 | a0001c0005t0015g0321a0001c0005t0015g0366a0001c0005t0017g0369others(4): Show | 7 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+139G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307037 | ||||||
| chr5:180307075
|
G | A | 22 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0006g0375others(19): Show | 23 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1674+101C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307075 | ||||||
| chr5:180307084
|
C | T | 27 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0001g0205others(24): Show | 28 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1674+92G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307084 | ||||||
| chr5:180307092
|
A | G | 2 | a0005c0010t0002g0256a0005c0010t0002g0257 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1674+84T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307092 | ||||||
| chr5:180307110
|
C | A | 27 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0001g0205others(24): Show | 28 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1674+66G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307110 | ||||||
| chr5:180307139
|
T | C | 121 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0001g0205others(118): Show | 127 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.1674+37A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307139 | ||||||
| chr5:180307145
|
GTGGGGGT others(6): Show |
G | 114 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0001g0205others(111): Show | 120 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1674+18_1674+30del others(13): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307145 | ||||||
| chr5:180307312
|
T | C | 86 | a0001c0005t0003g0134a0002c0002t0003g0002a0002c0002t0003g0007others(83): Show | 91 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1547-9A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307312 | ||||||
| chr5:180307326
|
G | A | 1 | a0001c0005t0005g0043 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1547-23C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307326 | ||||||
| chr5:180307373
|
A | AT | 20 | a0001c0005t0004g0114a0001c0005t0004g0129a0001c0005t0004g0130others(17): Show | 20 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1547-71dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307373 | ||||||
| chr5:180307528
|
A | C | 127 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(124): Show | 135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1547-225T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307528 | ||||||
| chr5:180307587
|
CAG | C | 74 | a0001c0001t0002g0324a0001c0003t0001g0065a0001c0003t0001g0078others(71): Show | 79 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1547-286_1547-285d others(4): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307587 | ||||||
| chr5:180307591
|
G | C | 1 | a0002c0002t0003g0133 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1547-288C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307591 | ||||||
| chr5:180307637
|
C | T | 1 | a0001c0004t0001g0077 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1547-334G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307637 | ||||||
| chr5:180307827
|
T | G | 7 | a0002c0002t0003g0059a0002c0002t0003g0066a0002c0002t0003g0067others(4): Show | 7 | NA18970.hp2 NA18971.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.1547-524A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307827 | ||||||
| chr5:180307884
|
G | A | 51 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(48): Show | 54 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1547-581C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307884 | ||||||
| chr5:180307928
|
T | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0124others(5): Show | 10 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1547-625A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307928 | ||||||
| chr5:180307969
|
G | T | 1 | a0001c0021t0002g0271 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1547-666C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307969 | ||||||
| chr5:180307978
|
T | C | 25 | a0001c0004t0001g0190a0001c0004t0001g0205a0001c0004t0001g0206others(22): Show | 26 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.1547-675A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307978 | ||||||
| chr5:180308031
|
C | T | 48 | a0001c0001t0001g0148a0001c0004t0001g0004a0001c0004t0001g0010others(45): Show | 51 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1547-728G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308031 | ||||||
| chr5:180308038
|
C | T | 25 | a0001c0004t0001g0190a0001c0004t0001g0205a0001c0004t0001g0206others(22): Show | 26 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.1547-735G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308038 | ||||||
| chr5:180308078
|
G | A | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(287): Show | 307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1547-775C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308078 | ||||||
| chr5:180308113
|
G | A | 72 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(69): Show | 77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1547-810C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308113 | ||||||
| chr5:180308124
|
C | T | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-821G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308124 | ||||||
| chr5:180308129
|
G | A | 26 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0001g0205others(23): Show | 27 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.1547-826C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308129 | ||||||
| chr5:180308168
|
G | A | 1 | a0002c0008t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1547-865C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308168 | ||||||
| chr5:180308188
|
G | A | 3 | a0001c0004t0001g0245a0001c0004t0002g0258a0001c0004t0002g0285 | 3 | HG02647.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1547-885C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308188 | ||||||
| chr5:180308204
|
T | C | 1 | a0001c0021t0002g0271 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1547-901A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308204 | ||||||
| chr5:180308213
|
A | G | 114 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0001g0245others(111): Show | 120 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1547-910T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308213 | ||||||
| chr5:180308217
|
C | T | 6 | a0001c0004t0001g0004a0001c0004t0001g0081a0001c0004t0001g0089others(3): Show | 7 | HG00438.hp2 HG02040.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1547-914G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308217 | ||||||
| chr5:180308255
|
C | CA | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-953_1547-952i others(3): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308255 | ||||||
| chr5:180308256
|
G | A | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-953C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308256 | ||||||
| chr5:180308256
|
G | GA | 11 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0001g0205others(8): Show | 11 | HG02451.hp1 HG02630.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1547-954dupT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308256 | ||||||
| chr5:180308269
|
G | A | 1 | a0002c0002t0003g0096 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1547-966C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308269 | ||||||
| chr5:180308270
|
A | G | 1 | a0002c0002t0003g0096 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1547-967T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308270 | ||||||
| chr5:180308359
|
C | T | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(132): Show | 142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1547-1056G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308359 | ||||||
| chr5:180308366
|
G | A | 19 | a0001c0005t0005g0023a0001c0005t0005g0027a0001c0005t0005g0029others(16): Show | 19 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1547-1063C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308366 | ||||||
| chr5:180308449
|
A | C | 162 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(159): Show | 170 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1547-1146T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308449 | ||||||
| chr5:180308547
|
C | T | 30 | a0001c0001t0002g0299a0001c0001t0014g0305a0001c0005t0001g0207others(27): Show | 30 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1547-1244G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308547 | ||||||
| chr5:180308548
|
G | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(132): Show | 142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1547-1245C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308548 | ||||||
| chr5:180308674
|
A | G | 76 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(73): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1547-1371T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308674 | ||||||
| chr5:180308695
|
A | T | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-1392T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308695 | ||||||
| chr5:180308763
|
T | C | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(132): Show | 142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1547-1460A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308763 | ||||||
| chr5:180308792
|
C | A | 19 | a0001c0005t0005g0023a0001c0005t0005g0027a0001c0005t0005g0029others(16): Show | 19 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1547-1489G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308792 | ||||||
| chr5:180308873
|
C | CT | 108 | a0001c0003t0001g0231a0001c0003t0006g0387a0001c0004t0001g0205others(105): Show | 113 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1547-1571dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308873 | ||||||
| chr5:180308873
|
C | CTT | 6 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0006g0375others(3): Show | 6 | HG02056.hp2 HG02451.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1547-1572_1547-157 others(6): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308873 | ||||||
| chr5:180308898
|
C | G | 27 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0001g0205others(24): Show | 28 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1547-1595G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308898 | ||||||
| chr5:180308910
|
C | T | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(26): Show | 31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1547-1607G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308910 | ||||||
| chr5:180308941
|
C | A | 11 | a0002c0002t0003g0092a0002c0002t0003g0093a0002c0002t0003g0094others(8): Show | 11 | HG00438.hp1 HG00597.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.1547-1638G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308941 | ||||||
| chr5:180308954
|
C | T | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(132): Show | 142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1547-1651G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308954 | ||||||
| chr5:180308959
|
A | G | 164 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(161): Show | 173 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1547-1656T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308959 | ||||||
| chr5:180309043
|
T | A | 1 | a0001c0001t0002g0359 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1547-1740A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309043 | ||||||
| chr5:180309123
|
C | T | 22 | a0001c0004t0030g0368a0001c0005t0005g0023a0001c0005t0005g0027others(19): Show | 22 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1547-1820G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309123 | ||||||
| chr5:180309193
|
A | G | 162 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(159): Show | 170 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1547-1890T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309193 | ||||||
| chr5:180309224
|
G | A | 1 | a0002c0002t0003g0139 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1547-1921C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309224 | ||||||
| chr5:180309341
|
A | C | 1 | a0001c0003t0002g0252 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1547-2038T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309341 | ||||||
| chr5:180309367
|
A | G | 106 | a0001c0005t0003g0107a0001c0005t0003g0134a0001c0005t0005g0023others(103): Show | 111 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1547-2064T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309367 | ||||||
| chr5:180309414
|
G | C | 1 | a0001c0009t0002g0367 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1547-2111C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309414 | ||||||
| chr5:180309454
|
CTT | C | 87 | a0001c0005t0003g0107a0001c0005t0003g0134a0002c0002t0003g0002others(84): Show | 92 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1547-2153_1547-215 others(6): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309454 | ||||||
| chr5:180309483
|
T | G | 1 | a0003c0006t0012g0173 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1547-2180A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309483 | ||||||
| chr5:180309512
|
C | T | 2 | a0001c0001t0002g0299a0001c0005t0029g0370 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1547-2209G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309512 | ||||||
| chr5:180309613
|
C | T | 320 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(317): Show | 337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.1547-2310G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309613 | ||||||
| chr5:180309631
|
C | T | 1 | a0001c0004t0001g0245 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1547-2328G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309631 | ||||||
| chr5:180309657
|
T | C | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(132): Show | 142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1547-2354A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309657 | ||||||
| chr5:180309742
|
T | C | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-2439A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309742 | ||||||
| chr5:180309755
|
G | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(132): Show | 142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1547-2452C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309755 | ||||||
| chr5:180309816
|
C | CT | 29 | a0001c0001t0002g0351a0001c0001t0014g0305a0001c0005t0001g0207others(26): Show | 29 | HG01123.hp2 HG01167.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1547-2514dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309816 | ||||||
| chr5:180309839
|
A | C | 261 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(258): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1547-2536T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309839 | ||||||
| chr5:180309842
|
A | G | 261 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(258): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1547-2539T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309842 | ||||||
| chr5:180309936
|
G | A | 261 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(258): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1546+2494C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309936 | ||||||
| chr5:180309959
|
C | T | 1 | a0001c0004t0001g0180 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1546+2471G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309959 | ||||||
| chr5:180309960
|
A | G | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(133): Show | 143 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1546+2470T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309960 | ||||||
| chr5:180309967
|
C | T | 4 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+2463G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309967 | ||||||
| chr5:180310000
|
C | T | 2 | a0002c0002t0003g0057a0002c0002t0003g0058 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1546+2430G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310000 | ||||||
| chr5:180310012
|
A | G | 261 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(258): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1546+2418T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310012 | ||||||
| chr5:180310032
|
G | A | 1 | a0001c0004t0001g0076 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1546+2398C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310032 | ||||||
| chr5:180310104
|
C | T | 20 | a0001c0005t0005g0023a0001c0005t0005g0027a0001c0005t0005g0029others(17): Show | 20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1546+2326G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310104 | ||||||
| chr5:180310106
|
A | G | 320 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(317): Show | 337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.1546+2324T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310106 | ||||||
| chr5:180310125
|
G | A | 1 | a0001c0001t0006g0378 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1546+2305C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310125 | ||||||
| chr5:180310141
|
C | T | 2 | a0003c0006t0001g0232a0003c0006t0002g0014 | 3 | HG00099.hp1 HG03239.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1546+2289G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310141 | ||||||
| chr5:180310256
|
G | C | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(287): Show | 307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1546+2174C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310256 | ||||||
| chr5:180310560
|
G | A | 2 | a0001c0004t0001g0205a0001c0004t0001g0206 | 2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1546+1870C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310560 | ||||||
| chr5:180310630
|
C | T | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(26): Show | 31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1546+1800G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310630 | ||||||
| chr5:180310659
|
C | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(132): Show | 142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1546+1771G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310659 | ||||||
| chr5:180310698
|
ACCGCG | A | 27 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0001g0205others(24): Show | 28 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1546+1727_1546+173 others(9): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310698 | ||||||
| chr5:180310738
|
G | T | 1 | a0001c0012t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1546+1692C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310738 | ||||||
| chr5:180310756
|
C | A | 116 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(113): Show | 123 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1546+1674G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310756 | ||||||
| chr5:180310793
|
G | A | 3 | a0001c0004t0030g0368a0005c0010t0002g0256a0005c0010t0002g0257 | 3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1546+1637C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310793 | ||||||
| chr5:180310832
|
C | CA | 49 | a0001c0001t0001g0090a0001c0001t0001g0138a0001c0001t0001g0169others(46): Show | 49 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+1597dupT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310832
|
C | CAA | 38 | a0001c0001t0002g0348a0001c0001t0006g0385a0001c0005t0004g0114others(35): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1546+1596_1546+159 others(6): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310832
|
C | CAAA | 41 | a0001c0001t0006g0381a0001c0005t0003g0134a0001c0005t0004g0165others(38): Show | 42 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1546+1595_1546+159 others(7): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310832
|
C | CAAAA | 9 | a0001c0005t0003g0107a0002c0002t0003g0069a0002c0002t0003g0133others(6): Show | 9 | HG01257.hp1 HG01358.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1546+1594_1546+159 others(8): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310832
|
CA | C | 27 | a0001c0001t0001g0006a0001c0001t0001g0124a0001c0001t0001g0125others(24): Show | 28 | HG00609.hp1 HG00642.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1546+1597delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310832
|
CAA | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0126others(17): Show | 21 | HG01258.hp1 HG01515.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1546+1596_1546+159 others(6): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310832
|
CAAA | C | 7 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546+1595_1546+159 others(7): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310832
|
CAAAA | C | 52 | a0001c0003t0001g0085a0001c0003t0001g0086a0001c0003t0001g0168others(49): Show | 56 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1546+1594_1546+159 others(8): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310832
|
CAAAAA | C | 61 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0102others(58): Show | 65 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1546+1593_1546+159 others(9): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310832
|
CAAAAAA | C | 9 | a0001c0003t0001g0218a0001c0003t0001g0241a0001c0003t0001g0242others(6): Show | 9 | HG00140.hp1 HG01192.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+1592_1546+159 others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310832
|
CAAAAAAA others(2): Show |
C | 11 | a0003c0006t0001g0224a0003c0006t0001g0225a0003c0006t0001g0226others(8): Show | 12 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(9): Show |
intron_variant | MODIFIER | c.1546+1589_1546+159 others(13): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310832
|
CAAAAAAA others(3): Show |
C | 1 | a0003c0006t0001g0223 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1546+1588_1546+159 others(14): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310832
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0004t0001g0187a0001c0004t0002g0013a0002c0002t0003g0210 | 4 | HG01952.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+1586_1546+159 others(16): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | ||||||
| chr5:180310863
|
A | T | 2 | a0001c0004t0001g0187a0001c0004t0002g0013 | 3 | HG01952.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1546+1567T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310863 | ||||||
| chr5:180310864
|
A | T | 2 | a0001c0003t0001g0188a0001c0003t0002g0322 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1546+1566T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310864 | ||||||
| chr5:180310865
|
T | A | 9 | a0001c0005t0004g0192a0001c0005t0004g0193a0001c0005t0004g0195others(6): Show | 9 | HG01167.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1546+1565A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310865 | ||||||
| chr5:180310873
|
A | G | 3 | a0001c0001t0002g0283a0001c0001t0002g0338a0001c0001t0002g0343 | 3 | HG01099.hp2 HG01934.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1546+1557T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310873 | ||||||
| chr5:180310891
|
T | C | 50 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(47): Show | 53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1546+1539A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310891 | ||||||
| chr5:180310927
|
C | T | 30 | a0001c0001t0002g0299a0001c0001t0014g0305a0001c0005t0001g0207others(27): Show | 30 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1546+1503G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310927 | ||||||
| chr5:180310977
|
G | T | 5 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0006g0375others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+1453C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310977 | ||||||
| chr5:180311025
|
T | G | 1 | a0003c0006t0001g0233 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1546+1405A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311025 | ||||||
| chr5:180311085
|
T | C | 5 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0006g0375others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+1345A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311085 | ||||||
| chr5:180311087
|
G | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(26): Show | 31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1546+1343C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311087 | ||||||
| chr5:180311101
|
A | G | 248 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(245): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1546+1329T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311101 | ||||||
| chr5:180311149
|
G | A | 5 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0006g0375others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+1281C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311149 | ||||||
| chr5:180311162
|
T | C | 190 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(187): Show | 200 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.1546+1268A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311162 | ||||||
| chr5:180311213
|
C | T | 87 | a0001c0005t0003g0107a0001c0005t0003g0134a0002c0002t0003g0002others(84): Show | 92 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1546+1217G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311213 | ||||||
| chr5:180311237
|
T | C | 50 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(47): Show | 53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1546+1193A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311237 | ||||||
| chr5:180311257
|
C | T | 1 | a0002c0002t0009g0295 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1546+1173G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311257 | ||||||
| chr5:180311278
|
A | G | 3 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384 | 3 | HG02145.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1546+1152T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311278 | ||||||
| chr5:180311437
|
T | G | 30 | a0001c0001t0002g0299a0001c0001t0014g0305a0001c0005t0001g0207others(27): Show | 30 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1546+993A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311437 | ||||||
| chr5:180311440
|
T | C | 1 | a0001c0005t0006g0380 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1546+990A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311440 | ||||||
| chr5:180311517
|
T | C | 187 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(184): Show | 198 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.1546+913A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311517 | ||||||
| chr5:180311638
|
A | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(116): Show | 126 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1546+792T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311638 | ||||||
| chr5:180311713
|
C | A | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(135): Show | 145 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1546+717G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311713 | ||||||
| chr5:180311715
|
G | A | 3 | a0001c0004t0030g0368a0005c0010t0002g0256a0005c0010t0002g0257 | 3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1546+715C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311715 | ||||||
| chr5:180311717
|
GA | G | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(135): Show | 145 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1546+712delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311717 | ||||||
| chr5:180311727
|
T | A | 1 | a0002c0002t0003g0204 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1546+703A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311727 | ||||||
| chr5:180311743
|
G | A | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(133): Show | 143 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1546+687C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311743 | ||||||
| chr5:180311782
|
G | A | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(133): Show | 143 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1546+648C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311782 | ||||||
| chr5:180311796
|
G | A | 1 | a0001c0003t0002g0320 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1546+634C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311796 | ||||||
| chr5:180311800
|
A | G | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(135): Show | 145 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1546+630T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311800 | ||||||
| chr5:180311925
|
G | A | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(133): Show | 142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1546+505C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311925 | ||||||
| chr5:180311984
|
AGGCAGGG others(17): Show |
A | 90 | a0001c0004t0030g0368a0001c0005t0003g0107a0001c0005t0003g0134others(87): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1546+422_1546+445d others(26): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311984 | ||||||
| chr5:180311988
|
AGGGAGGT others(33): Show |
A | 76 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(73): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1546+402_1546+441d others(42): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311988 | ||||||
| chr5:180312008
|
G | GACCAGGG others(1): Show |
47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(44): Show | 49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+421_1546+422i others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312008 | ||||||
| chr5:180312009
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+421C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312009 | ||||||
| chr5:180312010
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+420C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312010 | ||||||
| chr5:180312030
|
G | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(25): Show | 30 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1546+400C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312030 | ||||||
| chr5:180312034
|
G | T | 90 | a0001c0004t0030g0368a0001c0005t0003g0107a0001c0005t0003g0134others(87): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1546+396C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312034 | ||||||
| chr5:180312035
|
T | C | 49 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(46): Show | 53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1546+395A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312035 | ||||||
| chr5:180312036
|
G | GAGGACCA others(8): Show |
1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+393_1546+394i others(17): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312036 | ||||||
| chr5:180312049
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+381C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312049 | ||||||
| chr5:180312050
|
G | A | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(44): Show | 49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+380C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312050 | ||||||
| chr5:180312050
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+380C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312050 | ||||||
| chr5:180312050
|
GCAGGGAG others(49): Show |
G | 3 | a0001c0004t0002g0258a0001c0004t0002g0285a0001c0017t0001g0220 | 3 | HG02647.hp1 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1546+324_1546+379d others(58): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312050 | ||||||
| chr5:180312058
|
G | GCAGGGAG others(49): Show |
1 | a0002c0008t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1546+371_1546+372i others(58): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312058 | ||||||
| chr5:180312066
|
GCGGGGAG others(33): Show |
G | 90 | a0001c0004t0030g0368a0001c0005t0003g0107a0001c0005t0003g0134others(87): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1546+324_1546+363d others(42): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312066 | ||||||
| chr5:180312068
|
G | A | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(44): Show | 49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+362C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312068 | ||||||
| chr5:180312068
|
GGGGAGGC others(17): Show |
G | 49 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(46): Show | 53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1546+338_1546+361d others(26): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312068 | ||||||
| chr5:180312074
|
GCTGAGGA others(1): Show |
G | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(44): Show | 49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+348_1546+355d others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312074 | ||||||
| chr5:180312084
|
A | G | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(44): Show | 49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+346T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312084 | ||||||
| chr5:180312091
|
C | T | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(44): Show | 49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+339G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312091 | ||||||
| chr5:180312092
|
A | G | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(44): Show | 49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+338T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312092 | ||||||
| chr5:180312114
|
G | GCAGGGAG others(9): Show |
1 | a0002c0008t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1546+315_1546+316i others(18): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312114 | ||||||
| chr5:180312116
|
A | G | 91 | a0001c0001t0001g0183a0001c0004t0030g0368a0001c0005t0003g0107others(88): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1546+314T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312116 | ||||||
| chr5:180312121
|
G | A | 90 | a0001c0004t0030g0368a0001c0005t0003g0107a0001c0005t0003g0134others(87): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1546+309C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312121 | ||||||
| chr5:180312123
|
C | CAGGGAGG others(9): Show |
1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+306_1546+307i others(18): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312123 | ||||||
| chr5:180312123
|
C | T | 91 | a0001c0003t0001g0146a0001c0004t0030g0368a0001c0005t0003g0107others(88): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1546+307G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312123 | ||||||
| chr5:180312124
|
GGGGAGGC others(17): Show |
G | 4 | a0001c0003t0001g0146a0001c0009t0001g0172a0001c0009t0002g0367others(1): Show | 4 | HG02145.hp2 HG02622.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546+282_1546+305d others(26): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312124 | ||||||
| chr5:180312124
|
GGGGAGGC others(73): Show |
G | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(44): Show | 49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+226_1546+305d others(82): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312124 | ||||||
| chr5:180312137
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+293T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312137 | ||||||
| chr5:180312138
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+292G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312138 | ||||||
| chr5:180312156
|
T | A | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+274A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312156 | ||||||
| chr5:180312158
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+272T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312158 | ||||||
| chr5:180312160
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+270C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312160 | ||||||
| chr5:180312161
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+269T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312161 | ||||||
| chr5:180312162
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+268G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312162 | ||||||
| chr5:180312164
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+266T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312164 | ||||||
| chr5:180312164
|
AGGGAGGC others(25): Show |
A | 72 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(69): Show | 77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1546+234_1546+265d others(34): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312164 | ||||||
| chr5:180312171
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+259G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312171 | ||||||
| chr5:180312172
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+258T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312172 | ||||||
| chr5:180312172
|
AGGGAGGC others(17): Show |
A | 87 | a0001c0005t0003g0107a0001c0005t0003g0134a0002c0002t0003g0002others(84): Show | 92 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1546+234_1546+257d others(26): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312172 | ||||||
| chr5:180312186
|
C | CCAGGGAG others(425): Show |
1 | a0002c0008t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1546+243_1546+244i others(434): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312186 | ||||||
| chr5:180312196
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+234C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312196 | ||||||
| chr5:180312196
|
G | GGGGAGGC others(1): Show |
49 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(46): Show | 53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1546+226_1546+233d others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312196 | ||||||
| chr5:180312196
|
GGGGAGGC others(1): Show |
G | 10 | a0001c0001t0002g0283a0001c0001t0002g0338a0001c0001t0002g0343others(7): Show | 10 | HG01099.hp2 HG01934.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.1546+226_1546+233d others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312196 | ||||||
| chr5:180312204
|
A | G | 165 | a0001c0001t0001g0183a0001c0003t0001g0065a0001c0003t0001g0078others(162): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.1546+226T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312204 | ||||||
| chr5:180312231
|
G | C | 1 | a0001c0004t0001g0056 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1546+199C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312231 | ||||||
| chr5:180312241
|
A | AG | 10 | a0002c0002t0003g0097a0002c0002t0003g0111a0002c0002t0003g0136others(7): Show | 10 | HG00597.hp1 HG01175.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.1546+188dupC | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312241 | ||||||
| chr5:180312244
|
G | T | 1 | a0001c0005t0003g0107 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1546+186C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312244 | ||||||
| chr5:180312247
|
A | G | 86 | a0001c0005t0003g0107a0001c0005t0003g0134a0002c0002t0003g0002others(83): Show | 91 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1546+183T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312247 | ||||||
| chr5:180312247
|
A | T | 1 | a0002c0002t0003g0120 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1546+183T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312247 | ||||||
| chr5:180312256
|
C | T | 3 | a0001c0004t0030g0368a0005c0010t0002g0256a0005c0010t0002g0257 | 3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1546+174G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312256 | ||||||
| chr5:180312557
|
A | G | 1 | a0001c0003t0002g0252 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1432-13T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312557 | ||||||
| chr5:180312826
|
G | C | 1 | a0002c0008t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1432-282C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312826 | ||||||
| chr5:180312836
|
G | A | 3 | a0001c0004t0030g0368a0005c0010t0002g0256a0005c0010t0002g0257 | 3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1432-292C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312836 | ||||||
| chr5:180312839
|
C | T | 1 | a0002c0002t0009g0255 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1432-295G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312839 | ||||||
| chr5:180312858
|
C | A | 1 | a0001c0001t0006g0379 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1432-314G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312858 | ||||||
| chr5:180312867
|
A | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(116): Show | 126 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1432-323T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312867 | ||||||
| chr5:180312925
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(29): Show | 34 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.1432-381G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312925 | ||||||
| chr5:180312926
|
G | A | 3 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384 | 3 | HG02145.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1432-382C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312926 | ||||||
| chr5:180312942
|
A | G | 4 | a0002c0002t0003g0068a0002c0002t0003g0069a0002c0002t0003g0244others(1): Show | 4 | HG00558.hp1 NA18945.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1432-398T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312942 | ||||||
| chr5:180312951
|
G | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(116): Show | 126 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1432-407C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312951 | ||||||
| chr5:180312958
|
G | A | 19 | a0001c0005t0005g0023a0001c0005t0005g0027a0001c0005t0005g0029others(16): Show | 19 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1432-414C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312958 | ||||||
| chr5:180312959
|
T | G | 1 | a0003c0013t0001g0228 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1432-415A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312959 | ||||||
| chr5:180312989
|
A | C | 124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(121): Show | 131 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1432-445T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312989 | ||||||
| chr5:180313020
|
C | A | 1 | a0002c0008t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1432-476G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313020 | ||||||
| chr5:180313020
|
C | G | 294 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(291): Show | 311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1432-476G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313020 | ||||||
| chr5:180313023
|
T | C | 148 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(145): Show | 155 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1432-479A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313023 | ||||||
| chr5:180313046
|
G | A | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1432-502C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313046 | ||||||
| chr5:180313066
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(29): Show | 34 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.1432-522G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313066 | ||||||
| chr5:180313073
|
G | T | 1 | a0002c0008t0001g0216 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1432-529C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313073 | ||||||
| chr5:180313074
|
G | C | 5 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0006g0375others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1432-530C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313074 | ||||||
| chr5:180313080
|
G | A | 124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(121): Show | 131 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1432-536C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313080 | ||||||
| chr5:180313098
|
C | T | 9 | a0001c0005t0004g0192a0001c0005t0004g0193a0001c0005t0004g0195others(6): Show | 9 | HG01167.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1432-554G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313098 | ||||||
| chr5:180313100
|
G | A | 1 | a0001c0005t0031g0377 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1432-556C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313100 | ||||||
| chr5:180313100
|
G | C | 2 | a0001c0004t0001g0004a0001c0004t0001g0178 | 3 | NA18969.hp1 NA18981.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1432-556C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313100 | ||||||
| chr5:180313108
|
C | T | 93 | a0001c0003t0001g0209a0001c0005t0001g0207a0001c0005t0003g0107others(90): Show | 98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1432-564G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313108 | ||||||
| chr5:180313146
|
C | T | 6 | a0003c0006t0001g0223a0003c0006t0001g0224a0003c0006t0001g0225others(3): Show | 6 | NA18946.hp1 NA18966.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1432-602G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313146 | ||||||
| chr5:180313223
|
C | T | 1 | a0001c0004t0002g0365 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1431+584G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313223 | ||||||
| chr5:180313239
|
G | A | 94 | a0001c0005t0001g0207a0001c0005t0003g0107a0001c0005t0003g0134others(91): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1431+568C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313239 | ||||||
| chr5:180313337
|
A | G | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(26): Show | 31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1431+470T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313337 | ||||||
| chr5:180313366
|
C | T | 94 | a0001c0005t0001g0207a0001c0005t0003g0107a0001c0005t0003g0134others(91): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1431+441G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313366 | ||||||
| chr5:180313382
|
G | C | 4 | a0002c0002t0003g0068a0002c0002t0003g0069a0002c0002t0003g0244others(1): Show | 4 | HG00558.hp1 NA18945.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1431+425C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313382 | ||||||
| chr5:180313392
|
C | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG00544.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1431+415G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313392 | ||||||
| chr5:180313398
|
C | T | 316 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(313): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1431+409G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313398 | ||||||
| chr5:180313401
|
C | T | 1 | a0001c0003t0002g0302 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1431+406G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313401 | ||||||
| chr5:180313402
|
T | C | 1 | a0001c0003t0002g0362 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1431+405A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313402 | ||||||
| chr5:180313416
|
C | T | 1 | a0001c0003t0002g0302 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1431+391G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313416 | ||||||
| chr5:180313420
|
T | C | 165 | a0001c0004t0001g0004a0001c0004t0001g0056a0001c0004t0001g0060others(162): Show | 172 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.1431+387A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313420 | ||||||
| chr5:180313451
|
T | C | 77 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(74): Show | 82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1431+356A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313451 | ||||||
| chr5:180313453
|
T | C | 75 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(72): Show | 80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1431+354A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313453 | ||||||
| chr5:180313455
|
G | GT | 77 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(74): Show | 82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1431+351_1431+352i others(3): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313455 | ||||||
| chr5:180313459
|
G | A | 3 | a0001c0001t0002g0283a0001c0001t0002g0338a0001c0001t0002g0343 | 3 | HG01099.hp2 HG01934.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1431+348C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313459 | ||||||
| chr5:180313462
|
T | C | 238 | a0001c0001t0001g0186a0001c0001t0002g0299a0001c0001t0014g0305others(235): Show | 249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.1431+345A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313462 | ||||||
| chr5:180313469
|
A | G | 196 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(193): Show | 208 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.1431+338T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313469 | ||||||
| chr5:180313478
|
T | G | 1 | a0002c0008t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1431+329A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313478 | ||||||
| chr5:180313507
|
G | T | 1 | a0001c0001t0002g0343 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1431+300C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313507 | ||||||
| chr5:180313526
|
C | G | 5 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0006g0375others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1431+281G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313526 | ||||||
| chr5:180313527
|
T | C | 2 | a0001c0004t0001g0205a0001c0004t0001g0206 | 2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1431+280A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313527 | ||||||
| chr5:180313527
|
T | G | 91 | a0001c0005t0003g0107a0001c0005t0003g0134a0001c0005t0004g0113others(88): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1431+280A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313527 | ||||||
| chr5:180313539
|
G | A | 27 | a0001c0001t0014g0305a0001c0004t0002g0258a0001c0004t0002g0285others(24): Show | 27 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1431+268C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313539 | ||||||
| chr5:180313546
|
C | T | 1 | a0001c0005t0029g0370 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1431+261G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313546 | ||||||
| chr5:180313550
|
C | A | 4 | a0002c0002t0003g0057a0002c0002t0003g0058a0002c0002t0003g0137others(1): Show | 4 | HG01943.hp1 HG03130.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1431+257G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313550 | ||||||
| chr5:180313552
|
T | A | 4 | a0002c0002t0003g0057a0002c0002t0003g0058a0002c0002t0003g0137others(1): Show | 4 | HG01943.hp1 HG03130.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1431+255A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313552 | ||||||
| chr5:180313563
|
C | G | 118 | a0001c0001t0002g0299a0001c0001t0014g0305a0001c0003t0001g0065others(115): Show | 123 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1431+244G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313563 | ||||||
| chr5:180313576
|
T | C | 55 | a0001c0001t0001g0126a0001c0001t0001g0186a0001c0004t0001g0004others(52): Show | 59 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1431+231A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313576 | ||||||
| chr5:180313606
|
T | TAAAATA | 94 | a0001c0004t0001g0082a0001c0005t0001g0207a0001c0005t0003g0107others(91): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1431+195_1431+200d others(8): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313606 | ||||||
| chr5:180313626
|
A | T | 3 | a0001c0001t0018g0372a0001c0001t0018g0373a0001c0001t0021g0020 | 3 | HG03491.hp1 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1431+181T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313626 | ||||||
| chr5:180313640
|
C | T | 170 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(167): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1431+167G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313640 | ||||||
| chr5:180313646
|
T | G | 4 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1431+161A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313646 | ||||||
| chr5:180313705
|
G | A | 20 | a0001c0001t0006g0374a0001c0001t0006g0376a0001c0004t0002g0258others(17): Show | 20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1431+102C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313705 | ||||||
| chr5:180314131
|
T | C | 2 | a0002c0002t0003g0111a0002c0002t0003g0155 | 2 | HG01175.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1274-167A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314131 | ||||||
| chr5:180314327
|
G | C | 1 | a0001c0004t0006g0375 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1274-363C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314327 | ||||||
| chr5:180314374
|
C | A | 168 | a0001c0001t0001g0138a0001c0003t0001g0065a0001c0003t0001g0078others(165): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1274-410G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314374 | ||||||
| chr5:180314411
|
A | C | 275 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(272): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.1274-447T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314411 | ||||||
| chr5:180314446
|
A | G | 5 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0006g0375others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1274-482T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314446 | ||||||
| chr5:180314448
|
T | C | 76 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(73): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1274-484A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314448 | ||||||
| chr5:180314534
|
A | G | 105 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(102): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1274-570T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314534 | ||||||
| chr5:180314564
|
A | G | 3 | a0001c0003t0001g0117a0001c0003t0001g0118a0001c0003t0001g0119 | 3 | HG00280.hp2 HG00323.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1274-600T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314564 | ||||||
| chr5:180314633
|
C | T | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1274-669G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314633 | ||||||
| chr5:180314659
|
A | T | 3 | a0001c0004t0001g0070a0001c0004t0001g0071a0001c0004t0001g0077 | 3 | HG01934.hp2 HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1274-695T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314659 | ||||||
| chr5:180314765
|
C | T | 5 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0006g0375others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1274-801G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314765 | ||||||
| chr5:180314879
|
T | G | 2 | a0001c0004t0001g0245a0001c0005t0001g0207 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1274-915A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314879 | ||||||
| chr5:180314894
|
C | T | 25 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(22): Show | 25 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1274-930G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314894 | ||||||
| chr5:180314899
|
C | T | 1 | a0002c0002t0003g0137 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1274-935G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314899 | ||||||
| chr5:180314981
|
C | T | 89 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(86): Show | 94 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1274-1017G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314981 | ||||||
| chr5:180315022
|
C | T | 25 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(22): Show | 25 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1274-1058G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315022 | ||||||
| chr5:180315030
|
C | A | 1 | a0001c0001t0002g0330 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1274-1066G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315030 | ||||||
| chr5:180315161
|
G | A | 20 | a0001c0001t0006g0378a0001c0005t0005g0023a0001c0005t0005g0027others(17): Show | 20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1273+1180C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315161 | ||||||
| chr5:180315169
|
G | GTTTTTC | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1273+1166_1273+117 others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315169 | ||||||
| chr5:180315181
|
C | CT | 9 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384others(6): Show | 9 | HG02145.hp2 HG02148.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1273+1159dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315181 | ||||||
| chr5:180315181
|
C | CTTTTCT | 19 | a0001c0005t0005g0023a0001c0005t0005g0027a0001c0005t0005g0029others(16): Show | 19 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1273+1159_1273+116 others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315181 | ||||||
| chr5:180315201
|
G | A | 41 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(38): Show | 42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+1140C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315201 | ||||||
| chr5:180315204
|
G | A | 41 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(38): Show | 42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+1137C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315204 | ||||||
| chr5:180315208
|
C | T | 1 | a0001c0001t0002g0350 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1273+1133G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315208 | ||||||
| chr5:180315227
|
G | T | 41 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(38): Show | 42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+1114C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315227 | ||||||
| chr5:180315233
|
A | T | 4 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+1108T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315233 | ||||||
| chr5:180315240
|
C | T | 158 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(155): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1273+1101G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315240 | ||||||
| chr5:180315252
|
A | G | 20 | a0001c0001t0014g0305a0001c0005t0004g0114a0001c0005t0004g0129others(17): Show | 20 | HG01167.hp2 HG02071.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.1273+1089T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315252 | ||||||
| chr5:180315262
|
C | G | 24 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(21): Show | 24 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1273+1079G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315262 | ||||||
| chr5:180315263
|
C | T | 41 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(38): Show | 42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+1078G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315263 | ||||||
| chr5:180315279
|
G | A | 283 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(280): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.1273+1062C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315279 | ||||||
| chr5:180315329
|
C | T | 25 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(22): Show | 25 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1273+1012G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315329 | ||||||
| chr5:180315334
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1273+1007G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315334 | ||||||
| chr5:180315347
|
G | T | 41 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(38): Show | 42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+994C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315347 | ||||||
| chr5:180315379
|
T | C | 1 | a0001c0001t0006g0386 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1273+962A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315379 | ||||||
| chr5:180315384
|
G | T | 1 | a0001c0001t0006g0386 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1273+957C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315384 | ||||||
| chr5:180315389
|
A | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG01884.hp2 HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1273+952T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315389 | ||||||
| chr5:180315414
|
G | A | 24 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(21): Show | 24 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1273+927C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315414 | ||||||
| chr5:180315425
|
A | G | 1 | a0001c0021t0002g0271 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1273+916T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315425 | ||||||
| chr5:180315430
|
A | G | 1 | a0001c0021t0002g0271 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1273+911T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315430 | ||||||
| chr5:180315460
|
G | A | 41 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(38): Show | 42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+881C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315460 | ||||||
| chr5:180315468
|
G | A | 41 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(38): Show | 42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+873C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315468 | ||||||
| chr5:180315469
|
C | T | 1 | a0001c0005t0006g0380 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1273+872G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315469 | ||||||
| chr5:180315474
|
G | A | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1273+867C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315474 | ||||||
| chr5:180315530
|
T | C | 14 | a0001c0001t0001g0149a0001c0001t0001g0169a0001c0001t0001g0186others(11): Show | 15 | HG00280.hp1 HG02818.hp1 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.1273+811A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315530 | ||||||
| chr5:180315609
|
G | A | 20 | a0001c0001t0014g0305a0001c0005t0004g0114a0001c0005t0004g0129others(17): Show | 20 | HG01167.hp2 HG02071.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.1273+732C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315609 | ||||||
| chr5:180315628
|
A | G | 41 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(38): Show | 42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+713T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315628 | ||||||
| chr5:180315723
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1273+618C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315723 | ||||||
| chr5:180315934
|
A | G | 1 | a0001c0004t0001g0070 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1273+407T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315934 | ||||||
| chr5:180315988
|
T | C | 41 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(38): Show | 42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+353A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315988 | ||||||
| chr5:180315990
|
C | T | 41 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(38): Show | 42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+351G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315990 | ||||||
| chr5:180316032
|
C | T | 39 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(36): Show | 40 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1273+309G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316032 | ||||||
| chr5:180316084
|
G | A | 41 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(38): Show | 42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+257C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316084 | ||||||
| chr5:180316087
|
A | G | 48 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(45): Show | 52 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1273+254T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316087 | ||||||
| chr5:180316101
|
C | A | 41 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(38): Show | 42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+240G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316101 | ||||||
| chr5:180316174
|
C | T | 25 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(22): Show | 25 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1273+167G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316174 | ||||||
| chr5:180316205
|
C | A | 1 | a0001c0005t0011g0298 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1273+136G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316205 | ||||||
| chr5:180316218
|
C | T | 14 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(11): Show | 15 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(12): Show |
intron_variant | MODIFIER | c.1273+123G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316218 | ||||||
| chr5:180316260
|
G | T | 16 | a0001c0018t0028g0325a0003c0006t0001g0062a0003c0006t0001g0223others(13): Show | 17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1273+81C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316260 | ||||||
| chr5:180316272
|
T | A | 25 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(22): Show | 25 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1273+69A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316272 | ||||||
| chr5:180316294
|
C | T | 1 | a0001c0005t0029g0370 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1273+47G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316294 | ||||||
| chr5:180316308
|
T | C | 3 | a0001c0004t0030g0368a0005c0010t0002g0256a0005c0010t0002g0257 | 3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1273+33A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316308 | ||||||
| chr5:180316541
|
C | A | 1 | a0001c0004t0002g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1153-80G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316541 | ||||||
| chr5:180316553
|
C | T | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(26): Show | 31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1153-92G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316553 | ||||||
| chr5:180316569
|
A | G | 1 | a0002c0007t0002g0333 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1153-108T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316569 | ||||||
| chr5:180316637
|
C | T | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(26): Show | 31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1152+127G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316637 | ||||||
| chr5:180316730
|
C | T | 23 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(20): Show | 25 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1152+34G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316730 | ||||||
| chr5:180316731
|
G | A | 90 | a0001c0001t0001g0138a0001c0004t0001g0180a0001c0005t0003g0107others(87): Show | 95 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1152+33C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316731 | ||||||
| chr5:180316733
|
C | T | 1 | a0001c0003t0002g0267 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1152+31G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316733 | ||||||
| chr5:180316948
|
G | A | 7 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0001g0245others(4): Show | 7 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054+15C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 11/18 | chr5 | 180316948 | ||||||
| chr5:180317270
|
A | G | 1 | a0001c0004t0002g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.959-212T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317270 | ||||||
| chr5:180317364
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.959-306G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317364 | ||||||
| chr5:180317384
|
C | G | 4 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.959-326G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317384 | ||||||
| chr5:180317446
|
C | A | 1 | a0001c0001t0002g0281 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.959-388G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317446 | ||||||
| chr5:180317455
|
T | C | 70 | a0001c0003t0001g0065a0001c0003t0001g0078a0001c0003t0001g0085others(67): Show | 75 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.959-397A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317455 | ||||||
| chr5:180317459
|
C | T | 2 | a0001c0003t0002g0290a0001c0003t0002g0314 | 2 | NA19084.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.959-401G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317459 | ||||||
| chr5:180317464
|
TAAAAACC others(301): Show |
T | 4 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.959-714_959-407del | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317464 | ||||||
| chr5:180317488
|
A | G | 88 | a0001c0001t0001g0138a0001c0004t0001g0180a0001c0005t0003g0107others(85): Show | 92 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.959-430T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317488 | ||||||
| chr5:180317503
|
T | C | 2 | a0001c0001t0002g0339a0001c0001t0002g0340 | 2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.959-445A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317503 | ||||||
| chr5:180317509
|
CAGCACTT others(5): Show |
C | 1 | a0002c0002t0009g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.959-463_959-452del others(12): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317509 | ||||||
| chr5:180317525
|
C | T | 8 | a0001c0004t0001g0056a0001c0004t0001g0061a0001c0004t0001g0075others(5): Show | 8 | HG00639.hp1 HG01106.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.959-467G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317525 | ||||||
| chr5:180317529
|
G | A | 6 | a0001c0004t0001g0056a0001c0004t0001g0061a0001c0004t0001g0075others(3): Show | 6 | HG00639.hp1 HG01106.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.959-471C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317529 | ||||||
| chr5:180317531
|
G | A | 1 | a0001c0003t0001g0132 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.959-473C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317531 | ||||||
| chr5:180317534
|
C | T | 1 | a0001c0003t0002g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.959-476G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317534 | ||||||
| chr5:180317535
|
G | A | 2 | a0001c0004t0002g0258a0001c0004t0002g0285 | 2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.959-477C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317535 | ||||||
| chr5:180317544
|
A | G | 5 | a0001c0001t0006g0386a0001c0003t0002g0273a0001c0004t0001g0205others(2): Show | 5 | HG02630.hp1 HG02735.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.959-486T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317544 | ||||||
| chr5:180317555
|
C | G | 2 | a0002c0002t0003g0066a0002c0002t0003g0100 | 2 | NA18940.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.959-497G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317555 | ||||||
| chr5:180317555
|
C | T | 5 | a0001c0005t0004g0113a0001c0005t0004g0237a0001c0005t0004g0238others(2): Show | 5 | HG02717.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.959-497G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317555 | ||||||
| chr5:180317566
|
C | T | 80 | a0001c0001t0001g0124a0001c0001t0006g0386a0001c0003t0001g0065others(77): Show | 86 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.959-508G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317566 | ||||||
| chr5:180317573
|
A | C | 7 | a0001c0001t0006g0386a0001c0003t0001g0218a0001c0003t0001g0241others(4): Show | 7 | HG01192.hp2 HG02886.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.959-515T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317573 | ||||||
| chr5:180317576
|
A | G | 8 | a0001c0001t0006g0379a0001c0001t0006g0386a0001c0003t0001g0218others(5): Show | 8 | HG01192.hp2 HG02257.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.959-518T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317576 | ||||||
| chr5:180317586
|
C | T | 4 | a0002c0002t0003g0057a0002c0002t0003g0058a0002c0002t0003g0137others(1): Show | 4 | HG01943.hp1 HG03130.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.959-528G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317586 | ||||||
| chr5:180317639
|
G | C | 1 | a0001c0004t0001g0190 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.959-581C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317639 | ||||||
| chr5:180317650
|
T | G | 1 | a0001c0005t0015g0321 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.959-592A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317650 | ||||||
| chr5:180317708
|
G | A | 2 | a0001c0004t0001g0108a0001c0004t0001g0147 | 2 | HG02486.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.959-650C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317708 | ||||||
| chr5:180317714
|
G | C | 318 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(315): Show | 335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.959-656C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317714 | ||||||
| chr5:180317721
|
A | T | 318 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(315): Show | 335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.959-663T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317721 | ||||||
| chr5:180317723
|
C | T | 6 | a0001c0003t0002g0001a0001c0003t0002g0272a0001c0003t0002g0294others(3): Show | 9 | HG01070.hp2 HG01175.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.959-665G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317723 | ||||||
| chr5:180317746
|
A | G | 191 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(188): Show | 203 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.959-688T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317746 | ||||||
| chr5:180317758
|
C | CA | 8 | a0001c0001t0001g0169a0001c0001t0002g0296a0001c0001t0002g0313others(5): Show | 8 | HG01106.hp2 HG02738.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.959-701dupT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317758 | ||||||
| chr5:180317758
|
CA | C | 278 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(275): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.959-701delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317758 | ||||||
| chr5:180317889
|
G | C | 1 | a0002c0008t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.959-831C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317889 | ||||||
| chr5:180317901
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.959-843G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317901 | ||||||
| chr5:180317927
|
C | T | 1 | a0002c0002t0007g0046 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.958+866G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317927 | ||||||
| chr5:180317941
|
A | G | 4 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+852T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317941 | ||||||
| chr5:180317970
|
T | G | 4 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+823A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317970 | ||||||
| chr5:180318027
|
T | C | 4 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+766A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318027 | ||||||
| chr5:180318168
|
C | A | 4 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+625G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318168 | ||||||
| chr5:180318184
|
T | C | 2 | a0003c0014t0002g0307a0003c0014t0002g0319 | 2 | NA18946.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.958+609A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318184 | ||||||
| chr5:180318312
|
C | T | 1 | a0001c0005t0006g0380 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.958+481G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318312 | ||||||
| chr5:180318347
|
C | A | 27 | a0001c0004t0002g0258a0001c0004t0002g0285a0001c0005t0005g0023others(24): Show | 27 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.958+446G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318347 | ||||||
| chr5:180318385
|
G | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(26): Show | 31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.958+408C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318385 | ||||||
| chr5:180318389
|
C | T | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.958+404G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318389 | ||||||
| chr5:180318413
|
C | G | 88 | a0001c0001t0001g0138a0001c0004t0001g0180a0001c0005t0003g0107others(85): Show | 92 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.958+380G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318413 | ||||||
| chr5:180318437
|
C | A | 2 | a0001c0004t0001g0083a0001c0004t0002g0276 | 2 | HG00642.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.958+356G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318437 | ||||||
| chr5:180318461
|
C | T | 1 | a0002c0008t0001g0174 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.958+332G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318461 | ||||||
| chr5:180318515
|
G | A | 1 | a0001c0005t0005g0044 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.958+278C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318515 | ||||||
| chr5:180318534
|
GCAGCTGA others(2): Show |
G | 5 | a0001c0005t0006g0380a0001c0009t0001g0172a0001c0009t0002g0367others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.958+250_958+258del others(9): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318534 | ||||||
| chr5:180318549
|
G | C | 1 | a0001c0004t0002g0365 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.958+244C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318549 | ||||||
| chr5:180318607
|
A | G | 71 | a0001c0001t0001g0138a0001c0004t0001g0180a0002c0002t0001g0122others(68): Show | 74 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.958+186T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318607 | ||||||
| chr5:180318666
|
C | T | 7 | a0001c0004t0001g0185a0001c0004t0001g0190a0001c0004t0006g0382others(4): Show | 7 | HG02451.hp1 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.958+127G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318666 | ||||||
| chr5:180318721
|
C | CAG | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(44): Show | 49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.958+70_958+71dupCT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318721 | ||||||
| chr5:180318760
|
G | A | 3 | a0001c0003t0001g0117a0001c0003t0001g0118a0001c0003t0001g0119 | 3 | HG00280.hp2 HG00323.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.958+33C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318760 | ||||||
| chr5:180318963
|
C | T | 1 | a0002c0002t0003g0120 | 1 | NA18962.hp2 | splice_region_variant&intron_variant | LOW | c.795-7G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180318963 | ||||||
| chr5:180319098
|
G | A | 1 | a0001c0004t0001g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.795-142C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319098 | ||||||
| chr5:180319191
|
A | C | 4 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-235T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319191 | ||||||
| chr5:180319231
|
TATA | T | 25 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(22): Show | 25 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.795-278_795-276del others(3): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319231 | ||||||
| chr5:180319309
|
A | G | 5 | a0001c0005t0003g0134a0002c0002t0003g0123a0002c0002t0003g0135others(2): Show | 6 | HG01074.hp1 HG01261.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-353T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319309 | ||||||
| chr5:180319391
|
C | G | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(26): Show | 31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.795-435G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319391 | ||||||
| chr5:180319551
|
C | G | 1 | a0001c0001t0014g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.795-595G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319551 | ||||||
| chr5:180319708
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.795-752C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319708 | ||||||
| chr5:180319817
|
A | T | 23 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(20): Show | 23 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.795-861T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319817 | ||||||
| chr5:180319852
|
T | G | 26 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(23): Show | 26 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.795-896A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319852 | ||||||
| chr5:180320032
|
G | A | 1 | a0001c0005t0019g0388 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.795-1076C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320032 | ||||||
| chr5:180320100
|
C | A | 28 | a0001c0001t0002g0299a0001c0001t0014g0305a0001c0005t0004g0113others(25): Show | 28 | HG01167.hp2 HG02071.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.795-1144G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320100 | ||||||
| chr5:180320118
|
G | A | 1 | a0001c0003t0002g0266 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.795-1162C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320118 | ||||||
| chr5:180320149
|
T | C | 1 | a0001c0003t0026g0353 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.795-1193A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320149 | ||||||
| chr5:180320149
|
T | G | 2 | a0001c0004t0001g0245a0001c0005t0001g0207 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.795-1193A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320149 | ||||||
| chr5:180320154
|
G | A | 1 | a0001c0004t0001g0187 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.795-1198C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320154 | ||||||
| chr5:180320194
|
G | A | 1 | a0001c0004t0013g0052 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.795-1238C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320194 | ||||||
| chr5:180320235
|
G | A | 1 | a0001c0001t0002g0279 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.795-1279C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320235 | ||||||
| chr5:180320270
|
G | A | 2 | a0001c0001t0002g0299a0001c0005t0029g0370 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.795-1314C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320270 | ||||||
| chr5:180320282
|
G | A | 2 | a0001c0004t0001g0245a0001c0005t0001g0207 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.795-1326C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320282 | ||||||
| chr5:180320291
|
C | A | 2 | a0001c0001t0006g0374a0001c0001t0006g0376 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.795-1335G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320291 | ||||||
| chr5:180320363
|
C | A | 1 | a0001c0001t0001g0221 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.795-1407G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320363 | ||||||
| chr5:180320491
|
G | A | 24 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0004t0002g0258others(21): Show | 24 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.795-1535C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320491 | ||||||
| chr5:180320495
|
G | T | 40 | a0001c0004t0001g0004a0001c0004t0001g0010a0001c0004t0001g0011others(37): Show | 43 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.795-1539C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320495 | ||||||
| chr5:180320511
|
A | G | 324 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(321): Show | 341 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.795-1555T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320511 | ||||||
| chr5:180320539
|
A | G | 298 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(295): Show | 315 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.795-1583T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320539 | ||||||
| chr5:180320543
|
C | T | 1 | a0001c0001t0014g0305 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.795-1587G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320543 | ||||||
| chr5:180320564
|
G | C | 1 | a0001c0005t0005g0029 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.795-1608C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320564 | ||||||
| chr5:180320601
|
C | T | 1 | a0001c0004t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.795-1645G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320601 | ||||||
| chr5:180320809
|
G | C | 50 | a0001c0001t0001g0221a0001c0004t0001g0004a0001c0004t0001g0010others(47): Show | 54 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.795-1853C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320809 | ||||||
| chr5:180320888
|
G | A | 5 | a0001c0004t0001g0011a0001c0004t0001g0171a0001c0004t0001g0235others(2): Show | 6 | HG02074.hp1 HG02083.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-1932C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320888 | ||||||
| chr5:180320949
|
A | G | 1 | a0005c0010t0002g0257 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.795-1993T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320949 | ||||||
| chr5:180320967
|
A | ACTTTGTA others(27): Show |
1 | a0006c0016t0003g0063 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.795-2012_795-2011i others(36): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320967 | ||||||
| chr5:180320982
|
A | ATACAAAT others(26): Show |
1 | a0001c0005t0015g0366 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.795-2027_795-2026i others(35): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320982 | ||||||
| chr5:180320982
|
A | ATACAAAT others(26): Show |
254 | a0001c0001t0001g0054a0001c0001t0001g0138a0001c0001t0001g0150others(251): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.795-2059_795-2027d others(35): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320982 | ||||||
| chr5:180320982
|
A | ATACAAAT others(59): Show |
8 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(5): Show | 8 | HG02602.hp1 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.795-2092_795-2027d others(68): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320982 | ||||||
| chr5:180320982
|
A | G | 1 | a0006c0016t0003g0063 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.795-2026T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320982 | ||||||
| chr5:180321015
|
G | GTACAAAT others(59): Show |
8 | a0001c0003t0001g0188a0001c0004t0001g0185a0001c0004t0006g0382others(5): Show | 8 | HG02145.hp2 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.795-2060_795-2059i others(68): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321015 | ||||||
| chr5:180321127
|
T | C | 6 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-2171A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321127 | ||||||
| chr5:180321183
|
A | AT | 13 | a0001c0001t0001g0054a0001c0001t0001g0150a0001c0001t0001g0183others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.795-2228dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321183 | ||||||
| chr5:180321207
|
C | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0124others(135): Show | 146 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.795-2251G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321207 | ||||||
| chr5:180321300
|
G | A | 1 | a0001c0004t0004g0175 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.795-2344C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321300 | ||||||
| chr5:180321430
|
G | C | 20 | a0001c0001t0010g0038a0001c0005t0005g0023a0001c0005t0005g0027others(17): Show | 20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.795-2474C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321430 | ||||||
| chr5:180321454
|
T | C | 76 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0148others(73): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.795-2498A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321454 | ||||||
| chr5:180321591
|
C | T | 1 | a0001c0004t0001g0164 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.794+2597G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321591 | ||||||
| chr5:180321611
|
G | A | 1 | a0001c0004t0001g0056 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.794+2577C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321611 | ||||||
| chr5:180321631
|
T | C | 96 | a0001c0001t0001g0054a0001c0001t0001g0138a0001c0001t0001g0150others(93): Show | 100 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.794+2557A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321631 | ||||||
| chr5:180321690
|
A | G | 283 | a0001c0001t0001g0054a0001c0001t0001g0138a0001c0001t0001g0150others(280): Show | 297 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.794+2498T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321690 | ||||||
| chr5:180321758
|
G | A | 2 | a0001c0005t0004g0151a0001c0005t0004g0177 | 2 | HG02723.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.794+2430C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321758 | ||||||
| chr5:180321761
|
G | GGTTTT | 10 | a0001c0001t0001g0208a0001c0001t0002g0330a0001c0005t0004g0113others(7): Show | 10 | HG02145.hp2 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.794+2422_794+2426d others(7): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321761 | ||||||
| chr5:180321761
|
GGTTTT | G | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0124others(264): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.794+2422_794+2426d others(7): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321761 | ||||||
| chr5:180321761
|
GGTTTTGT others(3): Show |
G | 12 | a0001c0001t0001g0054a0001c0001t0001g0150a0001c0001t0001g0221others(9): Show | 13 | HG00639.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.794+2417_794+2426d others(12): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321761 | ||||||
| chr5:180321761
|
GGTTTTGT others(8): Show |
G | 21 | a0001c0001t0002g0282a0001c0003t0001g0188a0001c0003t0001g0231others(18): Show | 23 | HG00099.hp1 HG01433.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.794+2412_794+2426d others(17): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321761 | ||||||
| chr5:180321783
|
TTTTGTTT others(7): Show |
T | 1 | a0003c0006t0012g0173 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.794+2391_794+2404d others(16): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321783 | ||||||
| chr5:180321806
|
C | T | 10 | a0002c0002t0003g0092a0002c0002t0003g0093a0002c0002t0003g0094others(7): Show | 10 | HG00438.hp1 HG00597.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.794+2382G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321806 | ||||||
| chr5:180321815
|
G | A | 1 | a0001c0004t0001g0081 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.794+2373C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321815 | ||||||
| chr5:180321822
|
T | C | 4 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0005t0001g0207others(1): Show | 4 | HG02258.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+2366A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321822 | ||||||
| chr5:180321823
|
G | A | 3 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0005t0001g0207 | 3 | HG02630.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.794+2365C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321823 | ||||||
| chr5:180321901
|
A | G | 2 | a0001c0001t0001g0246a0001c0004t0001g0245 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.794+2287T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321901 | ||||||
| chr5:180321929
|
C | G | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2259G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321929 | ||||||
| chr5:180321930
|
T | C | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2258A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321930 | ||||||
| chr5:180321935
|
C | T | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2253G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321935 | ||||||
| chr5:180321949
|
G | A | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2239C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321949 | ||||||
| chr5:180321975
|
A | G | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2213T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321975 | ||||||
| chr5:180321978
|
C | G | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2210G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321978 | ||||||
| chr5:180321989
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.794+2199C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321989 | ||||||
| chr5:180321994
|
G | A | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2194C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321994 | ||||||
| chr5:180321998
|
A | C | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2190T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321998 | ||||||
| chr5:180322002
|
T | C | 1 | a0001c0001t0006g0374 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.794+2186A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322002 | ||||||
| chr5:180322019
|
T | C | 2 | a0001c0001t0006g0386a0001c0005t0004g0202 | 2 | HG02071.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794+2169A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322019 | ||||||
| chr5:180322023
|
A | G | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2165T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322023 | ||||||
| chr5:180322029
|
T | C | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2159A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322029 | ||||||
| chr5:180322030
|
G | A | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2158C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322030 | ||||||
| chr5:180322031
|
T | C | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2157A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322031 | ||||||
| chr5:180322054
|
T | C | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2134A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322054 | ||||||
| chr5:180322060
|
G | T | 1 | a0001c0005t0004g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2128C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322060 | ||||||
| chr5:180322067
|
G | A | 2 | a0001c0001t0006g0376a0001c0004t0006g0375 | 2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.794+2121C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322067 | ||||||
| chr5:180322260
|
G | A | 2 | a0001c0001t0001g0246a0001c0004t0001g0245 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.794+1928C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322260 | ||||||
| chr5:180322357
|
T | C | 1 | a0001c0004t0002g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.794+1831A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322357 | ||||||
| chr5:180322510
|
A | G | 1 | a0001c0001t0006g0386 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.794+1678T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322510 | ||||||
| chr5:180322546
|
A | G | 5 | a0001c0001t0006g0374a0001c0005t0023g0239a0002c0002t0008g0012others(2): Show | 6 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+1642T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322546 | ||||||
| chr5:180322604
|
G | A | 3 | a0001c0001t0002g0341a0001c0001t0002g0350a0001c0001t0002g0351 | 3 | HG01109.hp1 HG01123.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.794+1584C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322604 | ||||||
| chr5:180322728
|
C | CT | 4 | a0001c0001t0001g0246a0001c0004t0001g0245a0001c0004t0002g0013others(1): Show | 5 | HG02818.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+1459dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322728 | ||||||
| chr5:180322736
|
T | A | 3 | a0001c0004t0001g0081a0003c0006t0001g0229a0003c0006t0001g0230 | 3 | NA18968.hp2 NA18995.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.794+1452A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322736 | ||||||
| chr5:180322736
|
T | TA | 18 | a0001c0001t0002g0282a0001c0003t0001g0231a0001c0004t0006g0382others(15): Show | 19 | HG00099.hp1 HG01433.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.794+1451dupT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322736 | ||||||
| chr5:180322737
|
A | T | 163 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0124others(160): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.794+1451T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322737 | ||||||
| chr5:180322738
|
A | T | 3 | a0001c0001t0002g0264a0001c0001t0002g0280a0001c0001t0002g0281 | 3 | HG01257.hp2 HG01258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.794+1450T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322738 | ||||||
| chr5:180322861
|
C | A | 1 | a0002c0008t0001g0214 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.794+1327G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322861 | ||||||
| chr5:180322905
|
G | A | 11 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0006g0378others(8): Show | 11 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.794+1283C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322905 | ||||||
| chr5:180322967
|
G | A | 1 | a0001c0003t0002g0274 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.794+1221C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322967 | ||||||
| chr5:180322984
|
G | A | 39 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(36): Show | 39 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.794+1204C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322984 | ||||||
| chr5:180323237
|
G | A | 1 | a0001c0005t0004g0165 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.794+951C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323237 | ||||||
| chr5:180323315
|
G | A | 3 | a0001c0001t0001g0246a0001c0004t0001g0245a0001c0004t0002g0013 | 4 | HG02818.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+873C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323315 | ||||||
| chr5:180323336
|
C | T | 16 | a0001c0003t0001g0231a0001c0018t0028g0325a0002c0002t0009g0255others(13): Show | 16 | HG01975.hp1 HG03239.hp2 HG04199.hp2 others(13): Show |
intron_variant | MODIFIER | c.794+852G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323336 | ||||||
| chr5:180323337
|
G | A | 76 | a0001c0001t0001g0169a0001c0001t0001g0234a0001c0001t0002g0312others(73): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.794+851C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323337 | ||||||
| chr5:180323381
|
C | G | 1 | a0001c0004t0006g0382 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.794+807G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323381 | ||||||
| chr5:180323489
|
A | G | 3 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0003t0002g0286 | 3 | HG01433.hp1 HG03490.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.794+699T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323489 | ||||||
| chr5:180323550
|
G | C | 1 | a0001c0001t0002g0299 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.794+638C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323550 | ||||||
| chr5:180324111
|
A | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0124others(119): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.794+77T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180324111 | ||||||
| chr5:180324318
|
G | C | 1 | a0001c0005t0023g0239 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.677-13C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324318 | ||||||
| chr5:180324356
|
A | C | 4 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0005t0001g0207others(1): Show | 4 | HG02630.hp1 HG03195.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.677-51T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324356 | ||||||
| chr5:180324390
|
A | G | 53 | a0001c0001t0001g0221a0001c0003t0001g0085a0001c0003t0001g0086others(50): Show | 56 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.677-85T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324390 | ||||||
| chr5:180324402
|
G | T | 9 | a0001c0003t0001g0132a0002c0002t0003g0007a0002c0002t0003g0103others(6): Show | 10 | HG02135.hp1 HG02165.hp2 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.677-97C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324402 | ||||||
| chr5:180324441
|
C | T | 45 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0124others(42): Show | 48 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.677-136G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324441 | ||||||
| chr5:180324653
|
T | C | 1 | a0001c0005t0031g0377 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.676+163A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324653 | ||||||
| chr5:180324763
|
G | A | 1 | a0001c0001t0006g0374 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.676+53C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324763 | ||||||
| chr5:180325031
|
C | T | 34 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(31): Show | 34 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.597-136G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325031 | ||||||
| chr5:180325036
|
G | A | 1 | a0001c0005t0001g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597-141C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325036 | ||||||
| chr5:180325091
|
A | T | 3 | a0001c0001t0006g0374a0001c0001t0006g0376a0001c0004t0006g0375 | 3 | HG02809.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.597-196T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325091 | ||||||
| chr5:180325188
|
C | T | 3 | a0002c0002t0008g0012a0002c0002t0008g0247a0002c0002t0008g0248 | 4 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.597-293G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325188 | ||||||
| chr5:180325205
|
G | A | 1 | a0001c0005t0029g0370 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.597-310C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325205 | ||||||
| chr5:180325215
|
C | T | 199 | a0001c0001t0001g0054a0001c0001t0001g0138a0001c0001t0001g0150others(196): Show | 211 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.597-320G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325215 | ||||||
| chr5:180325277
|
G | A | 17 | a0001c0003t0001g0231a0001c0004t0006g0382a0001c0018t0028g0325others(14): Show | 17 | HG01975.hp1 HG02451.hp1 HG03239.hp2 others(14): Show |
intron_variant | MODIFIER | c.597-382C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325277 | ||||||
| chr5:180325367
|
C | G | 1 | a0001c0005t0004g0151 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.597-472G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325367 | ||||||
| chr5:180325477
|
G | A | 40 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(37): Show | 41 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.597-582C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325477 | ||||||
| chr5:180325504
|
C | T | 1 | a0002c0002t0020g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.597-609G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325504 | ||||||
| chr5:180325506
|
C | T | 1 | a0001c0005t0031g0377 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.597-611G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325506 | ||||||
| chr5:180325680
|
C | T | 3 | a0001c0009t0001g0172a0001c0009t0002g0367a0001c0009t0006g0384 | 3 | HG02145.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.597-785G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325680 | ||||||
| chr5:180325751
|
G | A | 3 | a0002c0002t0008g0012a0002c0002t0008g0247a0002c0002t0008g0248 | 4 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.597-856C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325751 | ||||||
| chr5:180325784
|
T | C | 18 | a0001c0001t0002g0282a0001c0003t0001g0231a0001c0018t0028g0325others(15): Show | 19 | HG00099.hp1 HG01433.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.597-889A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325784 | ||||||
| chr5:180325797
|
C | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0199others(1): Show | 4 | HG01884.hp2 HG02055.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.597-902G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325797 | ||||||
| chr5:180325896
|
G | A | 2 | a0001c0003t0002g0318a0001c0004t0002g0013 | 3 | HG00558.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.597-1001C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325896 | ||||||
| chr5:180326003
|
C | T | 2 | a0001c0003t0001g0189a0001c0004t0001g0190 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.597-1108G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326003 | ||||||
| chr5:180326024
|
C | CTAAA | 133 | a0001c0001t0001g0138a0001c0001t0001g0221a0001c0001t0002g0282others(130): Show | 140 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.597-1133_597-1130d others(6): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326024 | ||||||
| chr5:180326024
|
C | CTAAATAA others(1): Show |
6 | a0001c0001t0001g0186a0001c0004t0001g0076a0001c0004t0006g0382others(3): Show | 6 | HG02071.hp1 HG02451.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.597-1137_597-1130d others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326024 | ||||||
| chr5:180326024
|
CTAAATAA others(1): Show |
C | 5 | a0001c0001t0001g0246a0001c0004t0001g0245a0001c0004t0002g0013others(2): Show | 6 | HG02486.hp2 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.597-1137_597-1130d others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326024 | ||||||
| chr5:180326119
|
T | C | 327 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(324): Show | 345 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.597-1224A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326119 | ||||||
| chr5:180326179
|
A | T | 1 | a0001c0005t0003g0107 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.597-1284T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326179 | ||||||
| chr5:180326185
|
G | T | 261 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(258): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.597-1290C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326185 | ||||||
| chr5:180326218
|
G | T | 54 | a0001c0001t0001g0221a0001c0003t0001g0085a0001c0003t0001g0086others(51): Show | 57 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.597-1323C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326218 | ||||||
| chr5:180326220
|
A | T | 54 | a0001c0001t0001g0221a0001c0003t0001g0085a0001c0003t0001g0086others(51): Show | 57 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.597-1325T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326220 | ||||||
| chr5:180326221
|
A | T | 54 | a0001c0001t0001g0221a0001c0003t0001g0085a0001c0003t0001g0086others(51): Show | 57 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.597-1326T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326221 | ||||||
| chr5:180326305
|
T | C | 2 | a0001c0005t0017g0369a0001c0005t0017g0371 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.597-1410A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326305 | ||||||
| chr5:180326375
|
G | C | 2 | a0001c0005t0017g0369a0001c0005t0017g0371 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.597-1480C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326375 | ||||||
| chr5:180326418
|
T | G | 1 | a0001c0005t0031g0377 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.597-1523A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326418 | ||||||
| chr5:180326498
|
CAAT | C | 20 | a0001c0001t0010g0038a0001c0005t0005g0023a0001c0005t0005g0027others(17): Show | 20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.597-1606_597-1604d others(5): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326498 | ||||||
| chr5:180327006
|
G | A | 2 | a0001c0004t0002g0258a0001c0004t0002g0285 | 2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.596+1271C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327006 | ||||||
| chr5:180327131
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.596+1146C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327131 | ||||||
| chr5:180327236
|
G | A | 1 | a0002c0002t0003g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.596+1041C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327236 | ||||||
| chr5:180327291
|
C | T | 75 | a0001c0001t0001g0169a0001c0001t0001g0234a0001c0001t0002g0312others(72): Show | 80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.596+986G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327291 | ||||||
| chr5:180327373
|
C | A | 71 | a0001c0001t0001g0054a0001c0001t0001g0138a0001c0001t0001g0150others(68): Show | 75 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.596+904G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327373 | ||||||
| chr5:180327576
|
T | C | 2 | a0001c0001t0001g0149a0001c0005t0019g0388 | 2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.596+701A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327576 | ||||||
| chr5:180327657
|
T | C | 145 | a0001c0001t0001g0169a0001c0001t0001g0183a0001c0001t0001g0184others(142): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.596+620A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327657 | ||||||
| chr5:180327664
|
T | C | 1 | a0002c0002t0009g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.596+613A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327664 | ||||||
| chr5:180327685
|
G | A | 1 | a0001c0004t0001g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.596+592C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327685 | ||||||
| chr5:180327687
|
T | C | 1 | a0004c0011t0003g0008 | 2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.596+590A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327687 | ||||||
| chr5:180327715
|
C | A | 2 | a0001c0003t0001g0189a0001c0004t0001g0190 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.596+562G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327715 | ||||||
| chr5:180327758
|
C | T | 16 | a0001c0003t0001g0231a0001c0018t0028g0325a0002c0002t0009g0255others(13): Show | 16 | HG01975.hp1 HG03239.hp2 HG04199.hp2 others(13): Show |
intron_variant | MODIFIER | c.596+519G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327758 | ||||||
| chr5:180327776
|
T | C | 6 | a0001c0001t0001g0246a0001c0004t0001g0245a0001c0004t0002g0013others(3): Show | 7 | HG02074.hp1 HG02486.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.596+501A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327776 | ||||||
| chr5:180328071
|
C | CT | 18 | a0001c0001t0002g0282a0001c0003t0001g0231a0001c0005t0031g0377others(15): Show | 19 | HG00099.hp1 HG01433.hp2 HG03239.hp1 others(16): Show |
intron_variant | MODIFIER | c.596+205dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180328071 | ||||||
| chr5:180328071
|
CT | C | 70 | a0001c0001t0001g0221a0001c0001t0001g0246a0001c0001t0002g0297others(67): Show | 74 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.596+205delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180328071 | ||||||
| chr5:180328107
|
C | T | 2 | a0001c0005t0017g0369a0001c0005t0017g0371 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.596+170G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180328107 | ||||||
| chr5:180328118
|
G | C | 18 | a0001c0001t0002g0282a0001c0003t0001g0231a0001c0018t0028g0325others(15): Show | 19 | HG00099.hp1 HG01433.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.596+159C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180328118 | ||||||
| chr5:180328185
|
G | A | 2 | a0001c0001t0006g0376a0001c0004t0006g0375 | 2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.596+92C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180328185 | ||||||
| chr5:180328207
|
C | T | 1 | a0002c0002t0003g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.596+70G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180328207 | ||||||
| chr5:180328559
|
C | T | 21 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0006g0378others(18): Show | 21 | HG00280.hp1 HG01167.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.535-221G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180328559 | ||||||
| chr5:180328744
|
G | A | 1 | a0001c0004t0006g0382 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.535-406C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180328744 | ||||||
| chr5:180328805
|
T | G | 1 | a0001c0001t0014g0305 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.535-467A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180328805 | ||||||
| chr5:180328873
|
A | G | 39 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(36): Show | 39 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.535-535T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180328873 | ||||||
| chr5:180328973
|
G | A | 5 | a0001c0001t0001g0246a0001c0004t0001g0245a0001c0004t0002g0013others(2): Show | 6 | HG02486.hp2 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-635C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180328973 | ||||||
| chr5:180329001
|
C | T | 72 | a0001c0001t0001g0054a0001c0001t0001g0138a0001c0001t0001g0150others(69): Show | 76 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.535-663G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329001 | ||||||
| chr5:180329044
|
T | C | 1 | a0002c0002t0003g0103 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.535-706A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329044 | ||||||
| chr5:180329207
|
C | T | 3 | a0001c0001t0001g0208a0001c0003t0002g0289a0001c0012t0001g0116 | 3 | HG03471.hp2 NA19011.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.535-869G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329207 | ||||||
| chr5:180329208
|
G | A | 55 | a0001c0001t0001g0221a0001c0003t0001g0085a0001c0003t0001g0086others(52): Show | 58 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.535-870C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329208 | ||||||
| chr5:180329224
|
G | A | 2 | a0001c0005t0017g0369a0001c0005t0017g0371 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.535-886C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329224 | ||||||
| chr5:180329483
|
G | C | 2 | a0001c0005t0017g0369a0001c0005t0017g0371 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.535-1145C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329483 | ||||||
| chr5:180329804
|
G | A | 1 | a0001c0004t0001g0077 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.534+896C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329804 | ||||||
| chr5:180329809
|
G | C | 1 | a0001c0005t0011g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.534+891C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329809 | ||||||
| chr5:180329818
|
C | T | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0124others(26): Show | 32 | HG00140.hp2 HG01255.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.534+882G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329818 | ||||||
| chr5:180329826
|
C | T | 1 | a0002c0002t0003g0103 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.534+874G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329826 | ||||||
| chr5:180329994
|
G | A | 3 | a0002c0002t0008g0012a0002c0002t0008g0247a0002c0002t0008g0248 | 4 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+706C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329994 | ||||||
| chr5:180330031
|
A | C | 1 | a0001c0005t0023g0239 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.534+669T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330031 | ||||||
| chr5:180330031
|
A | G | 18 | a0001c0001t0002g0282a0001c0003t0001g0231a0001c0018t0028g0325others(15): Show | 19 | HG00099.hp1 HG01433.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.534+669T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330031 | ||||||
| chr5:180330073
|
C | T | 1 | a0001c0003t0002g0293 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.534+627G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330073 | ||||||
| chr5:180330187
|
G | A | 1 | a0001c0004t0001g0083 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.534+513C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330187 | ||||||
| chr5:180330188
|
G | C | 7 | a0001c0004t0001g0211a0001c0004t0001g0212a0001c0004t0001g0213others(4): Show | 7 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+512C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330188 | ||||||
| chr5:180330191
|
C | T | 1 | a0001c0003t0002g0320 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.534+509G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330191 | ||||||
| chr5:180330470
|
T | C | 7 | a0001c0004t0001g0211a0001c0004t0001g0212a0001c0004t0001g0213others(4): Show | 7 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+230A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330470 | ||||||
| chr5:180330486
|
C | T | 1 | a0002c0002t0003g0053 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.534+214G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330486 | ||||||
| chr5:180330675
|
T | G | 5 | a0002c0002t0003g0106a0002c0002t0003g0160a0002c0002t0003g0203others(2): Show | 5 | HG00140.hp2 HG01516.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+25A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330675 | ||||||
| chr5:180330883
|
C | T | 1 | a0001c0001t0006g0376 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.400-49G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180330883 | ||||||
| chr5:180331012
|
C | T | 4 | a0001c0004t0001g0089a0002c0002t0003g0112a0002c0002t0003g0120others(1): Show | 4 | HG00609.hp2 HG02040.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-178G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331012 | ||||||
| chr5:180331045
|
C | T | 8 | a0001c0001t0001g0246a0001c0001t0006g0376a0001c0004t0001g0245others(5): Show | 9 | HG02486.hp2 HG02818.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-211G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331045 | ||||||
| chr5:180331046
|
A | G | 8 | a0001c0001t0001g0246a0001c0001t0006g0376a0001c0004t0001g0245others(5): Show | 9 | HG02486.hp2 HG02818.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-212T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331046 | ||||||
| chr5:180331067
|
A | G | 8 | a0001c0001t0001g0246a0001c0001t0006g0376a0001c0004t0001g0245others(5): Show | 9 | HG02145.hp1 HG02486.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-233T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331067 | ||||||
| chr5:180331178
|
C | T | 1 | a0002c0002t0003g0106 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.399+317G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331178 | ||||||
| chr5:180331189
|
C | T | 1 | a0001c0004t0002g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.399+306G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331189 | ||||||
| chr5:180331205
|
G | A | 1 | a0001c0003t0002g0253 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.399+290C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331205 | ||||||
| chr5:180331295
|
A | G | 4 | a0001c0001t0002g0299a0001c0004t0001g0205a0001c0004t0001g0206others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+200T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331295 | ||||||
| chr5:180331323
|
T | C | 21 | a0001c0001t0014g0260a0001c0003t0001g0218a0001c0003t0001g0241others(18): Show | 21 | HG00558.hp1 HG02145.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.399+172A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331323 | ||||||
| chr5:180331608
|
T | A | 1 | a0001c0004t0006g0382 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.341-55A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331608 | ||||||
| chr5:180331710
|
G | A | 3 | a0001c0004t0002g0013a0001c0005t0017g0369a0001c0005t0017g0371 | 4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-157C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331710 | ||||||
| chr5:180331760
|
G | T | 1 | a0001c0004t0010g0034 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.341-207C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331760 | ||||||
| chr5:180331853
|
C | T | 1 | a0001c0003t0001g0168 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.341-300G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331853 | ||||||
| chr5:180331920
|
A | G | 10 | a0001c0003t0001g0209a0001c0004t0001g0211a0001c0004t0001g0212others(7): Show | 10 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.341-367T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331920 | ||||||
| chr5:180331921
|
A | G | 10 | a0001c0003t0001g0209a0001c0004t0001g0211a0001c0004t0001g0212others(7): Show | 10 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.341-368T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331921 | ||||||
| chr5:180331962
|
G | T | 3 | a0001c0004t0002g0013a0001c0005t0017g0369a0001c0005t0017g0371 | 4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-409C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331962 | ||||||
| chr5:180331985
|
G | A | 2 | a0001c0001t0002g0359a0001c0005t0002g0358 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.341-432C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331985 | ||||||
| chr5:180332077
|
A | T | 3 | a0001c0001t0010g0038a0001c0001t0010g0049a0002c0002t0022g0021 | 3 | HG02602.hp1 HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.341-524T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332077 | ||||||
| chr5:180332246
|
C | T | 2 | a0005c0010t0002g0256a0005c0010t0002g0257 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.341-693G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332246 | ||||||
| chr5:180332251
|
G | A | 1 | a0001c0005t0006g0380 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.341-698C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332251 | ||||||
| chr5:180332256
|
AGGGGGAT others(2): Show |
A | 32 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0183others(29): Show | 33 | HG00099.hp1 HG00280.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.341-712_341-704del others(9): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332256 | ||||||
| chr5:180332265
|
C | T | 6 | a0002c0002t0003g0092a0002c0002t0003g0094a0002c0002t0003g0095others(3): Show | 6 | HG00438.hp1 NA18941.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-712G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332265 | ||||||
| chr5:180332282
|
G | T | 1 | a0001c0003t0002g0362 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.341-729C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332282 | ||||||
| chr5:180332314
|
A | G | 5 | a0001c0001t0002g0299a0001c0004t0001g0205a0001c0004t0001g0206others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-761T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332314 | ||||||
| chr5:180332316
|
G | A | 5 | a0001c0001t0002g0299a0001c0004t0001g0205a0001c0004t0001g0206others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-763C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332316 | ||||||
| chr5:180332477
|
C | T | 6 | a0001c0001t0002g0299a0001c0004t0001g0205a0001c0004t0001g0206others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-924G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332477 | ||||||
| chr5:180332496
|
A | AT | 6 | a0001c0001t0002g0299a0001c0004t0001g0205a0001c0004t0001g0206others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-944dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332496 | ||||||
| chr5:180332526
|
A | G | 3 | a0003c0006t0001g0223a0003c0006t0001g0224a0003c0006t0001g0225 | 3 | NA18946.hp1 NA19068.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.341-973T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332526 | ||||||
| chr5:180332668
|
G | T | 1 | a0002c0002t0003g0106 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.341-1115C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332668 | ||||||
| chr5:180332698
|
C | T | 3 | a0002c0002t0008g0012a0002c0002t0008g0247a0002c0002t0008g0248 | 4 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-1145G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332698 | ||||||
| chr5:180332721
|
G | A | 1 | a0001c0001t0002g0344 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.341-1168C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332721 | ||||||
| chr5:180332760
|
G | A | 1 | a0001c0004t0001g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.341-1207C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332760 | ||||||
| chr5:180332810
|
G | A | 2 | a0001c0001t0002g0345a0001c0001t0002g0346 | 2 | HG00323.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.341-1257C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332810 | ||||||
| chr5:180332928
|
T | C | 72 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0183others(69): Show | 74 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.341-1375A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332928 | ||||||
| chr5:180333013
|
C | T | 27 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0183others(24): Show | 27 | HG00280.hp1 HG01167.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.341-1460G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333013 | ||||||
| chr5:180333120
|
T | C | 23 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0199others(20): Show | 23 | HG00140.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.341-1567A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333120 | ||||||
| chr5:180333129
|
C | A | 1 | a0001c0001t0002g0279 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.341-1576G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333129 | ||||||
| chr5:180333239
|
CT | C | 45 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(42): Show | 47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.341-1687delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333239 | ||||||
| chr5:180333298
|
G | A | 1 | a0001c0004t0006g0382 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.341-1745C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333298 | ||||||
| chr5:180333352
|
C | T | 1 | a0002c0002t0008g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.341-1799G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333352 | ||||||
| chr5:180333398
|
C | T | 1 | a0002c0002t0005g0048 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.341-1845G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333398 | ||||||
| chr5:180333463
|
C | T | 1 | a0001c0004t0001g0010 | 2 | HG00733.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.341-1910G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333463 | ||||||
| chr5:180333481
|
G | A | 1 | a0001c0004t0013g0052 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.341-1928C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333481 | ||||||
| chr5:180333481
|
G | T | 3 | a0001c0004t0002g0013a0001c0005t0017g0369a0001c0005t0017g0371 | 4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-1928C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333481 | ||||||
| chr5:180333525
|
T | C | 45 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(42): Show | 47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.341-1972A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333525 | ||||||
| chr5:180333548
|
TTTACA | T | 4 | a0001c0003t0002g0293a0001c0003t0002g0311a0001c0003t0002g0327others(1): Show | 4 | NA18612.hp2 NA18941.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-2000_341-1996d others(7): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333548 | ||||||
| chr5:180333567
|
T | C | 2 | a0001c0001t0006g0376a0001c0004t0006g0375 | 2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.341-2014A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333567 | ||||||
| chr5:180333593
|
C | T | 27 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0183others(24): Show | 27 | HG00280.hp1 HG01167.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.341-2040G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333593 | ||||||
| chr5:180333595
|
A | T | 45 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(42): Show | 47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.341-2042T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333595 | ||||||
| chr5:180333682
|
C | T | 41 | a0001c0001t0010g0038a0001c0001t0010g0049a0001c0003t0001g0231others(38): Show | 42 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.341-2129G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333682 | ||||||
| chr5:180333982
|
G | C | 1 | a0001c0005t0031g0377 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.340+1846C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333982 | ||||||
| chr5:180334163
|
G | C | 292 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0183others(289): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.340+1665C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334163 | ||||||
| chr5:180334182
|
C | T | 1 | a0001c0003t0002g0262 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.340+1646G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334182 | ||||||
| chr5:180334248
|
G | T | 45 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(42): Show | 47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.340+1580C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334248 | ||||||
| chr5:180334279
|
T | A | 9 | a0001c0003t0001g0209a0001c0004t0001g0211a0001c0004t0001g0212others(6): Show | 9 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+1549A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334279 | ||||||
| chr5:180334366
|
C | A | 3 | a0001c0001t0002g0299a0001c0003t0002g0352a0001c0003t0026g0353 | 3 | HG02451.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.340+1462G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334366 | ||||||
| chr5:180334424
|
C | T | 1 | a0001c0005t0008g0156 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.340+1404G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334424 | ||||||
| chr5:180334454
|
G | C | 41 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(38): Show | 42 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.340+1374C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334454 | ||||||
| chr5:180334499
|
A | G | 1 | a0001c0004t0001g0083 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.340+1329T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334499 | ||||||
| chr5:180334609
|
A | G | 6 | a0001c0001t0002g0299a0001c0004t0001g0205a0001c0004t0001g0206others(3): Show | 6 | HG02451.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+1219T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334609 | ||||||
| chr5:180334739
|
C | T | 1 | a0002c0002t0003g0105 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.340+1089G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334739 | ||||||
| chr5:180334769
|
C | T | 45 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(42): Show | 47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.340+1059G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334769 | ||||||
| chr5:180334985
|
G | A | 9 | a0001c0003t0001g0209a0001c0004t0001g0211a0001c0004t0001g0212others(6): Show | 9 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+843C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334985 | ||||||
| chr5:180335097
|
A | G | 292 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0183others(289): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.340+731T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335097 | ||||||
| chr5:180335254
|
A | G | 1 | a0001c0004t0002g0365 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.340+574T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335254 | ||||||
| chr5:180335289
|
C | T | 42 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(39): Show | 43 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.340+539G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335289 | ||||||
| chr5:180335360
|
C | G | 204 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0183others(201): Show | 216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.340+468G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335360 | ||||||
| chr5:180335405
|
T | C | 45 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(42): Show | 47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.340+423A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335405 | ||||||
| chr5:180335414
|
G | A | 1 | a0002c0002t0003g0053 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.340+414C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335414 | ||||||
| chr5:180335590
|
G | A | 3 | a0002c0002t0009g0360a0003c0014t0002g0307a0003c0014t0002g0319 | 3 | NA18946.hp2 NA19064.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.340+238C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335590 | ||||||
| chr5:180335601
|
C | T | 1 | a0001c0003t0002g0262 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.340+227G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335601 | ||||||
| chr5:180335752
|
C | A | 1 | a0001c0005t0008g0156 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.340+76G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335752 | ||||||
| chr5:180335799
|
C | T | 1 | a0001c0005t0001g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.340+29G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335799 | ||||||
| chr5:180335808
|
C | T | 1 | a0001c0004t0001g0245 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.340+20G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335808 | ||||||
| chr5:180336018
|
C | T | 27 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0183others(24): Show | 27 | HG00280.hp1 HG01167.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.215-65G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336018 | ||||||
| chr5:180336149
|
G | C | 1 | a0003c0006t0001g0233 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.215-196C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336149 | ||||||
| chr5:180336175
|
G | C | 1 | a0001c0005t0004g0238 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.215-222C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336175 | ||||||
| chr5:180336290
|
G | A | 41 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(38): Show | 42 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.214+189C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336290 | ||||||
| chr5:180336293
|
G | A | 1 | a0002c0002t0009g0255 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.214+186C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336293 | ||||||
| chr5:180336306
|
A | G | 1 | a0002c0002t0003g0123 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.214+173T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336306 | ||||||
| chr5:180336316
|
C | T | 3 | a0001c0004t0002g0013a0001c0005t0017g0369a0001c0005t0017g0371 | 4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+163G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336316 | ||||||
| chr5:180336319
|
T | C | 13 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0004t0001g0089others(10): Show | 13 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.214+160A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336319 | ||||||
| chr5:180336398
|
T | G | 292 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0183others(289): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.214+81A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336398 | ||||||
| chr5:180336768
|
A | G | 4 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0199others(1): Show | 4 | HG01884.hp2 HG02055.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-191T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336768 | ||||||
| chr5:180336776
|
G | A | 2 | a0001c0001t0001g0246a0001c0004t0001g0245 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.116-199C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336776 | ||||||
| chr5:180336789
|
C | T | 53 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0003t0001g0102others(50): Show | 58 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.116-212G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336789 | ||||||
| chr5:180336876
|
G | A | 27 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0183others(24): Show | 27 | HG00280.hp1 HG01167.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.116-299C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336876 | ||||||
| chr5:180336923
|
T | C | 45 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(42): Show | 47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.116-346A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336923 | ||||||
| chr5:180336935
|
G | A | 1 | a0001c0003t0001g0231 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.116-358C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336935 | ||||||
| chr5:180336952
|
G | A | 3 | a0001c0004t0002g0013a0001c0005t0017g0369a0001c0005t0017g0371 | 4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-375C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336952 | ||||||
| chr5:180337123
|
C | T | 2 | a0001c0001t0001g0246a0001c0004t0001g0245 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.116-546G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337123 | ||||||
| chr5:180337124
|
G | A | 1 | a0002c0015t0001g0009 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.116-547C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337124 | ||||||
| chr5:180337176
|
C | T | 9 | a0002c0002t0003g0092a0002c0002t0003g0093a0002c0002t0003g0094others(6): Show | 9 | HG00438.hp1 HG00597.hp1 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.116-599G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337176 | ||||||
| chr5:180337209
|
C | T | 1 | a0001c0005t0005g0029 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.116-632G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337209 | ||||||
| chr5:180337270
|
C | T | 42 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(39): Show | 43 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.116-693G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337270 | ||||||
| chr5:180337271
|
G | A | 1 | a0001c0005t0016g0306 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.116-694C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337271 | ||||||
| chr5:180337322
|
G | C | 1 | a0001c0004t0001g0180 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.116-745C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337322 | ||||||
| chr5:180337370
|
G | A | 7 | a0001c0005t0004g0113a0001c0005t0004g0237a0001c0005t0004g0238others(4): Show | 7 | HG02145.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.116-793C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337370 | ||||||
| chr5:180337378
|
A | G | 1 | a0002c0002t0003g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.116-801T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337378 | ||||||
| chr5:180337453
|
G | GAAA | 41 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(38): Show | 42 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.116-879_116-877dup others(3): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337453 | ||||||
| chr5:180337453
|
GA | G | 12 | a0001c0001t0002g0288a0001c0005t0004g0113a0001c0005t0004g0237others(9): Show | 13 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.116-877delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337453 | ||||||
| chr5:180337488
|
C | T | 1 | a0002c0002t0005g0048 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.116-911G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337488 | ||||||
| chr5:180337586
|
C | T | 2 | a0001c0004t0001g0205a0001c0004t0001g0206 | 2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.115+907G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337586 | ||||||
| chr5:180337612
|
G | A | 1 | a0003c0014t0002g0307 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.115+881C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337612 | ||||||
| chr5:180337616
|
G | A | 1 | a0001c0005t0005g0045 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.115+877C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337616 | ||||||
| chr5:180337621
|
A | G | 2 | a0001c0003t0001g0189a0001c0004t0001g0190 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.115+872T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337621 | ||||||
| chr5:180337660
|
GCCACCTC others(9): Show |
G | 27 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0183others(24): Show | 27 | HG00280.hp1 HG01167.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.115+817_115+832del others(16): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337660 | ||||||
| chr5:180337678
|
G | A | 27 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0183others(24): Show | 27 | HG00280.hp1 HG01167.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.115+815C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337678 | ||||||
| chr5:180337698
|
C | G | 120 | a0001c0001t0001g0219a0001c0001t0001g0234a0001c0001t0002g0003others(117): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.115+795G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337698 | ||||||
| chr5:180337709
|
T | C | 1 | a0001c0005t0031g0377 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.115+784A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337709 | ||||||
| chr5:180337779
|
C | T | 4 | a0001c0003t0002g0293a0001c0003t0002g0311a0001c0003t0002g0327others(1): Show | 4 | NA18612.hp2 NA18941.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+714G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337779 | ||||||
| chr5:180337926
|
C | T | 3 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0005t0001g0207 | 3 | HG02630.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.115+567G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337926 | ||||||
| chr5:180338019
|
A | C | 45 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(42): Show | 47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.115+474T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338019 | ||||||
| chr5:180338021
|
G | A | 1 | a0002c0002t0025g0251 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.115+472C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338021 | ||||||
| chr5:180338104
|
A | G | 45 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(42): Show | 47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.115+389T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338104 | ||||||
| chr5:180338291
|
G | A | 1 | a0001c0003t0001g0078 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.115+202C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338291 | ||||||
| chr5:180338377
|
C | T | 1 | a0001c0004t0002g0326 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.115+116G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338377 | ||||||
| chr5:180338413
|
AC | A | 8 | a0001c0001t0006g0386a0001c0001t0006g0389a0001c0001t0006g0390others(5): Show | 9 | HG00280.hp1 HG01099.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+79delG | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338413 | ||||||
| chr5:180338467
|
C | T | 173 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0246others(170): Show | 186 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.115+26G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338467 | ||||||
| chr5:180338662
|
G | A | 2 | a0001c0004t0001g0213a0001c0004t0001g0217 | 2 | NA18964.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.8-62C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180338662 | ||||||
| chr5:180338900
|
C | T | 12 | a0001c0003t0001g0231a0002c0002t0003g0053a0003c0006t0001g0223others(9): Show | 12 | HG01975.hp1 HG03239.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-300G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180338900 | ||||||
| chr5:180338949
|
T | C | 4 | a0001c0004t0001g0187a0001c0004t0001g0205a0001c0004t0001g0206others(1): Show | 4 | HG01952.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-349A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180338949 | ||||||
| chr5:180339061
|
G | A | 1 | a0001c0004t0001g0080 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.8-461C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339061 | ||||||
| chr5:180339082
|
A | T | 1 | a0006c0016t0003g0063 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.8-482T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339082 | ||||||
| chr5:180339107
|
C | A | 1 | a0003c0006t0001g0232 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.8-507G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339107 | ||||||
| chr5:180339131
|
G | A | 20 | a0001c0001t0001g0234a0001c0001t0006g0378a0001c0001t0006g0381others(17): Show | 22 | HG00280.hp1 HG01099.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.8-531C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339131 | ||||||
| chr5:180339177
|
C | G | 1 | a0002c0002t0003g0249 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.8-577G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339177 | ||||||
| chr5:180339317
|
T | A | 1 | a0001c0001t0006g0374 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8-717A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339317 | ||||||
| chr5:180339329
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0150 | 2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.8-729C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339329 | ||||||
| chr5:180339359
|
A | G | 9 | a0001c0003t0001g0209a0001c0004t0001g0211a0001c0004t0001g0212others(6): Show | 9 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-759T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339359 | ||||||
| chr5:180339378
|
C | CA | 49 | a0001c0001t0001g0182a0001c0001t0001g0194a0001c0001t0001g0234others(46): Show | 49 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.8-779dupT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339378 | ||||||
| chr5:180339378
|
C | CAA | 10 | a0001c0001t0001g0246a0001c0001t0006g0381a0001c0001t0018g0373others(7): Show | 10 | HG00558.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-780_8-779dupTT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339378 | ||||||
| chr5:180339378
|
CA | C | 68 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(65): Show | 71 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.8-779delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339378 | ||||||
| chr5:180339525
|
T | C | 1 | a0001c0004t0001g0082 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.8-925A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339525 | ||||||
| chr5:180339558
|
G | A | 1 | a0001c0003t0001g0218 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.8-958C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339558 | ||||||
| chr5:180339563
|
G | A | 1 | a0001c0005t0031g0377 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8-963C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339563 | ||||||
| chr5:180339781
|
C | T | 1 | a0002c0002t0003g0106 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.8-1181G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339781 | ||||||
| chr5:180339927
|
T | C | 45 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(42): Show | 46 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.8-1327A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339927 | ||||||
| chr5:180340091
|
A | G | 21 | a0001c0001t0001g0234a0001c0001t0006g0378a0001c0001t0006g0381others(18): Show | 23 | HG00280.hp1 HG01099.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.8-1491T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340091 | ||||||
| chr5:180340107
|
G | T | 1 | a0001c0004t0002g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.8-1507C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340107 | ||||||
| chr5:180340135
|
C | T | 2 | a0001c0001t0002g0275a0001c0004t0002g0276 | 2 | HG01070.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.8-1535G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340135 | ||||||
| chr5:180340137
|
G | A | 1 | a0003c0006t0001g0062 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.8-1537C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340137 | ||||||
| chr5:180340184
|
G | GT | 43 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(40): Show | 44 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.8-1585dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340184 | ||||||
| chr5:180340190
|
T | C | 1 | a0001c0004t0001g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.8-1590A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340190 | ||||||
| chr5:180340190
|
T | G | 31 | a0001c0001t0010g0038a0001c0001t0010g0049a0001c0003t0010g0028others(28): Show | 31 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.8-1590A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340190 | ||||||
| chr5:180340196
|
G | T | 1 | a0002c0002t0003g0210 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.8-1596C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340196 | ||||||
| chr5:180340198
|
T | G | 1 | a0002c0002t0003g0210 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.8-1598A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340198 | ||||||
| chr5:180340299
|
C | T | 3 | a0002c0002t0008g0012a0002c0002t0008g0247a0002c0002t0008g0248 | 4 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-1699G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340299 | ||||||
| chr5:180340309
|
C | A | 1 | a0001c0001t0014g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8-1709G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340309 | ||||||
| chr5:180340331
|
C | T | 1 | a0001c0001t0006g0389 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.8-1731G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340331 | ||||||
| chr5:180340332
|
G | A | 1 | a0001c0021t0002g0271 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.8-1732C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340332 | ||||||
| chr5:180340410
|
T | C | 5 | a0001c0004t0002g0013a0002c0002t0008g0012a0002c0002t0008g0247others(2): Show | 7 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1810A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340410 | ||||||
| chr5:180340426
|
G | A | 1 | a0001c0001t0006g0374 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8-1826C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340426 | ||||||
| chr5:180340511
|
G | GT | 77 | a0001c0001t0001g0194a0001c0001t0001g0234a0001c0001t0002g0312others(74): Show | 79 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.8-1912dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340511 | ||||||
| chr5:180340511
|
G | GTT | 18 | a0001c0001t0006g0385a0001c0001t0014g0305a0001c0003t0002g0001others(15): Show | 21 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.8-1913_8-1912dupAA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340511 | ||||||
| chr5:180340511
|
GT | G | 7 | a0001c0003t0001g0218a0001c0004t0001g0213a0001c0004t0001g0215others(4): Show | 7 | HG02735.hp2 HG03942.hp2 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-1912delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340511 | ||||||
| chr5:180340511
|
GTT | G | 42 | a0001c0001t0001g0221a0001c0001t0006g0374a0001c0003t0001g0065others(39): Show | 43 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.8-1913_8-1912delAA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340511 | ||||||
| chr5:180340575
|
C | G | 16 | a0001c0001t0001g0234a0001c0001t0006g0378a0001c0001t0006g0381others(13): Show | 16 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-1975G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340575 | ||||||
| chr5:180340597
|
C | T | 16 | a0001c0001t0001g0234a0001c0001t0006g0378a0001c0001t0006g0381others(13): Show | 16 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-1997G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340597 | ||||||
| chr5:180340605
|
A | G | 63 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0001t0001g0234others(60): Show | 66 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.8-2005T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340605 | ||||||
| chr5:180340680
|
T | C | 21 | a0001c0001t0001g0208a0001c0001t0001g0234a0001c0001t0006g0378others(18): Show | 23 | HG00280.hp1 HG01099.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.8-2080A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340680 | ||||||
| chr5:180340732
|
T | G | 1 | a0001c0012t0002g0261 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.8-2132A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340732 | ||||||
| chr5:180340765
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.8-2165G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340765 | ||||||
| chr5:180340815
|
C | T | 2 | a0001c0003t0002g0300a0001c0003t0002g0361 | 2 | NA19007.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.8-2215G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340815 | ||||||
| chr5:180340970
|
C | T | 1 | a0001c0001t0006g0374 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8-2370G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340970 | ||||||
| chr5:180341008
|
T | A | 2 | a0001c0001t0006g0376a0001c0004t0006g0375 | 2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.8-2408A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341008 | ||||||
| chr5:180341181
|
A | G | 16 | a0001c0001t0001g0234a0001c0001t0006g0378a0001c0001t0006g0381others(13): Show | 16 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-2581T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341181 | ||||||
| chr5:180341184
|
A | G | 283 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(280): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.8-2584T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341184 | ||||||
| chr5:180341193
|
T | C | 1 | a0002c0002t0009g0360 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.8-2593A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341193 | ||||||
| chr5:180341254
|
A | G | 4 | a0001c0003t0001g0241a0001c0003t0001g0242a0001c0003t0001g0243others(1): Show | 4 | HG00558.hp1 HG03710.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-2654T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341254 | ||||||
| chr5:180341334
|
T | G | 3 | a0001c0001t0002g0299a0001c0003t0002g0352a0001c0003t0026g0353 | 3 | HG02451.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.8-2734A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341334 | ||||||
| chr5:180341355
|
C | G | 2 | a0001c0004t0001g0205a0001c0004t0001g0206 | 2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.8-2755G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341355 | ||||||
| chr5:180341398
|
A | G | 66 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0324others(63): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.8-2798T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341398 | ||||||
| chr5:180341527
|
A | C | 22 | a0001c0001t0001g0208a0001c0001t0001g0234a0001c0001t0006g0378others(19): Show | 24 | HG00280.hp1 HG01099.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.8-2927T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341527 | ||||||
| chr5:180341599
|
G | A | 20 | a0001c0001t0001g0208a0001c0001t0006g0378a0001c0001t0006g0381others(17): Show | 22 | HG00280.hp1 HG01099.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.8-2999C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341599 | ||||||
| chr5:180341802
|
G | A | 1 | a0003c0006t0001g0233 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.8-3202C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341802 | ||||||
| chr5:180341859
|
C | T | 10 | a0001c0003t0001g0209a0001c0003t0001g0218a0001c0004t0001g0211others(7): Show | 10 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-3259G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341859 | ||||||
| chr5:180341911
|
G | C | 5 | a0001c0001t0002g0018a0001c0001t0002g0354a0001c0001t0002g0355others(2): Show | 6 | HG00735.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-3311C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341911 | ||||||
| chr5:180342345
|
C | T | 31 | a0001c0001t0010g0038a0001c0001t0010g0049a0001c0003t0010g0028others(28): Show | 31 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.8-3745G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342345 | ||||||
| chr5:180342378
|
A | C | 2 | a0001c0003t0001g0189a0001c0004t0001g0190 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.8-3778T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342378 | ||||||
| chr5:180342407
|
G | GT | 170 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0199others(167): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.8-3808dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342407 | ||||||
| chr5:180342407
|
G | GTT | 30 | a0001c0001t0002g0296a0001c0001t0002g0297a0001c0001t0002g0299others(27): Show | 31 | HG00099.hp2 HG00597.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.8-3809_8-3808dupAA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342407 | ||||||
| chr5:180342407
|
GT | G | 54 | a0001c0001t0001g0153a0001c0001t0001g0221a0001c0001t0006g0374others(51): Show | 55 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.8-3808delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342407 | ||||||
| chr5:180342407
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0005t0005g0047 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.8-3819_8-3808delAA others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342407 | ||||||
| chr5:180342415
|
T | G | 2 | a0001c0003t0001g0189a0001c0004t0001g0190 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.8-3815A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342415 | ||||||
| chr5:180342415
|
T | TG | 12 | a0001c0003t0001g0231a0002c0002t0003g0053a0003c0006t0001g0223others(9): Show | 12 | HG01975.hp1 HG03239.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-3816_8-3815insC | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342415 | ||||||
| chr5:180342627
|
C | T | 4 | a0001c0001t0002g0265a0001c0001t0002g0288a0001c0004t0001g0110others(1): Show | 4 | HG01255.hp2 NA18984.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-4027G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342627 | ||||||
| chr5:180342654
|
C | T | 1 | a0001c0003t0002g0286 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.8-4054G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342654 | ||||||
| chr5:180342658
|
T | C | 11 | a0001c0001t0001g0219a0001c0003t0001g0209a0001c0003t0001g0218others(8): Show | 11 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.8-4058A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342658 | ||||||
| chr5:180342697
|
C | G | 2 | a0001c0003t0002g0284a0001c0004t0002g0285 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.8-4097G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342697 | ||||||
| chr5:180342793
|
T | G | 2 | a0001c0005t0017g0369a0001c0005t0017g0371 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.8-4193A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342793 | ||||||
| chr5:180342964
|
G | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(120): Show | 129 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.8-4364C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342964 | ||||||
| chr5:180343047
|
T | G | 2 | a0001c0001t0006g0381a0001c0001t0006g0385 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.8-4447A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343047 | ||||||
| chr5:180343163
|
G | A | 2 | a0001c0005t0006g0380a0001c0005t0031g0377 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.8-4563C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343163 | ||||||
| chr5:180343243
|
C | T | 3 | a0001c0004t0006g0382a0001c0005t0019g0383a0001c0005t0019g0388 | 3 | HG02055.hp2 HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.8-4643G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343243 | ||||||
| chr5:180343258
|
C | T | 1 | a0001c0001t0006g0374 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8-4658G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343258 | ||||||
| chr5:180343554
|
G | A | 12 | a0001c0003t0001g0231a0002c0002t0003g0053a0003c0006t0001g0223others(9): Show | 12 | HG01975.hp1 HG03239.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-4954C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343554 | ||||||
| chr5:180343559
|
T | C | 11 | a0001c0001t0001g0219a0001c0003t0001g0209a0001c0003t0001g0218others(8): Show | 11 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.8-4959A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343559 | ||||||
| chr5:180343656
|
G | A | 1 | a0001c0003t0002g0357 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.8-5056C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343656 | ||||||
| chr5:180343757
|
A | G | 42 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(39): Show | 43 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.8-5157T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343757 | ||||||
| chr5:180343946
|
G | A | 1 | a0001c0004t0001g0083 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.8-5346C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343946 | ||||||
| chr5:180343983
|
C | T | 1 | a0001c0005t0019g0388 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.8-5383G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343983 | ||||||
| chr5:180344273
|
A | C | 1 | a0001c0009t0001g0172 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8-5673T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344273 | ||||||
| chr5:180344380
|
G | C | 2 | a0001c0001t0006g0376a0001c0004t0006g0375 | 2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.8-5780C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344380 | ||||||
| chr5:180344542
|
A | G | 4 | a0001c0005t0004g0237a0001c0005t0004g0238a0001c0005t0004g0240others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-5942T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344542 | ||||||
| chr5:180344750
|
G | A | 2 | a0001c0005t0006g0380a0001c0005t0031g0377 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.8-6150C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344750 | ||||||
| chr5:180344787
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.8-6187G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344787 | ||||||
| chr5:180344826
|
C | CT | 42 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(39): Show | 43 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.8-6227dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344826 | ||||||
| chr5:180344838
|
C | T | 1 | a0001c0004t0001g0164 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.8-6238G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344838 | ||||||
| chr5:180344847
|
G | C | 1 | a0001c0005t0031g0377 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8-6247C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344847 | ||||||
| chr5:180344849
|
A | G | 43 | a0001c0001t0001g0221a0001c0001t0006g0374a0001c0003t0001g0065others(40): Show | 44 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.8-6249T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344849 | ||||||
| chr5:180344851
|
C | T | 5 | a0001c0001t0006g0376a0001c0004t0001g0205a0001c0004t0001g0206others(2): Show | 5 | HG02630.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-6251G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344851 | ||||||
| chr5:180344882
|
C | A | 1 | a0001c0003t0001g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.8-6282G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344882 | ||||||
| chr5:180344993
|
C | T | 1 | a0001c0005t0004g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.8-6393G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344993 | ||||||
| chr5:180345020
|
A | T | 1 | a0001c0004t0002g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.8-6420T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345020 | ||||||
| chr5:180345062
|
C | T | 63 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0001t0006g0374others(60): Show | 66 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.8-6462G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345062 | ||||||
| chr5:180345087
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.8-6487G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345087 | ||||||
| chr5:180345259
|
C | T | 1 | a0001c0021t0002g0271 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.8-6659G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345259 | ||||||
| chr5:180345260
|
G | A | 1 | a0001c0004t0002g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.8-6660C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345260 | ||||||
| chr5:180345316
|
C | T | 1 | a0001c0005t0015g0366 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.8-6716G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345316 | ||||||
| chr5:180345324
|
C | T | 3 | a0001c0004t0030g0368a0001c0005t0017g0369a0001c0005t0017g0371 | 3 | HG02486.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.8-6724G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345324 | ||||||
| chr5:180345454
|
G | A | 2 | a0001c0001t0001g0246a0001c0004t0001g0245 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.8-6854C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345454 | ||||||
| chr5:180345494
|
T | C | 1 | a0001c0004t0001g0170 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.8-6894A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345494 | ||||||
| chr5:180345589
|
C | T | 1 | a0002c0002t0003g0161 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.8-6989G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345589 | ||||||
| chr5:180345618
|
C | T | 1 | a0002c0002t0003g0109 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.8-7018G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345618 | ||||||
| chr5:180345640
|
C | G | 63 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0001t0006g0374others(60): Show | 66 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.8-7040G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345640 | ||||||
| chr5:180345779
|
G | A | 2 | a0001c0001t0001g0246a0001c0004t0001g0245 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.8-7179C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345779 | ||||||
| chr5:180345834
|
C | T | 12 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0199others(9): Show | 12 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-7234G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345834 | ||||||
| chr5:180345835
|
A | G | 214 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(211): Show | 224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.8-7235T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345835 | ||||||
| chr5:180345954
|
C | T | 1 | a0001c0004t0001g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.7+7257G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345954 | ||||||
| chr5:180345972
|
C | T | 2 | a0001c0003t0001g0209a0002c0002t0003g0210 | 2 | HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.7+7239G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345972 | ||||||
| chr5:180345985
|
C | T | 3 | a0002c0002t0008g0012a0002c0002t0008g0247a0002c0002t0008g0248 | 4 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+7226G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345985 | ||||||
| chr5:180346019
|
A | G | 2 | a0001c0001t0014g0260a0001c0012t0002g0261 | 2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.7+7192T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346019 | ||||||
| chr5:180346292
|
C | G | 5 | a0001c0001t0001g0208a0001c0004t0002g0013a0002c0002t0008g0012others(2): Show | 7 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+6919G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346292 | ||||||
| chr5:180346543
|
G | A | 3 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0005t0001g0207 | 3 | HG02630.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7+6668C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346543 | ||||||
| chr5:180346558
|
C | T | 1 | a0002c0002t0007g0025 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.7+6653G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346558 | ||||||
| chr5:180346587
|
C | T | 1 | a0001c0001t0002g0279 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.7+6624G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346587 | ||||||
| chr5:180346667
|
CGCCCCTG others(2): Show |
C | 12 | a0001c0003t0001g0231a0002c0002t0003g0053a0003c0006t0001g0223others(9): Show | 12 | HG01975.hp1 HG03239.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.7+6535_7+6543delCC others(7): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346667 | ||||||
| chr5:180346802
|
C | G | 3 | a0001c0005t0011g0277a0001c0005t0011g0278a0001c0005t0029g0370 | 3 | HG02615.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7+6409G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346802 | ||||||
| chr5:180346857
|
A | G | 66 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0001t0001g0234others(63): Show | 69 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.7+6354T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346857 | ||||||
| chr5:180346904
|
G | T | 1 | a0002c0002t0003g0059 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7+6307C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346904 | ||||||
| chr5:180347065
|
A | C | 3 | a0001c0004t0002g0258a0005c0010t0002g0256a0005c0010t0002g0257 | 3 | HG02965.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.7+6146T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347065 | ||||||
| chr5:180347073
|
G | A | 3 | a0001c0001t0002g0359a0001c0005t0002g0358a0001c0005t0011g0254 | 3 | HG01884.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.7+6138C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347073 | ||||||
| chr5:180347139
|
G | A | 1 | a0002c0002t0003g0084 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.7+6072C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347139 | ||||||
| chr5:180347201
|
G | T | 1 | a0002c0002t0003g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.7+6010C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347201 | ||||||
| chr5:180347456
|
C | A | 12 | a0001c0003t0001g0231a0002c0002t0003g0053a0003c0006t0001g0223others(9): Show | 12 | HG01975.hp1 HG03239.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.7+5755G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347456 | ||||||
| chr5:180347458
|
G | T | 16 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0199others(13): Show | 16 | HG00140.hp2 HG01167.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.7+5753C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347458 | ||||||
| chr5:180347577
|
G | A | 5 | a0001c0001t0006g0386a0001c0001t0006g0389a0001c0001t0006g0390others(2): Show | 5 | HG00280.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+5634C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347577 | ||||||
| chr5:180347615
|
T | A | 1 | a0001c0005t0004g0157 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.7+5596A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347615 | ||||||
| chr5:180347642
|
T | C | 369 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(366): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.7+5569A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347642 | ||||||
| chr5:180347816
|
C | T | 1 | a0002c0002t0007g0024 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.7+5395G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347816 | ||||||
| chr5:180347845
|
G | A | 1 | a0002c0002t0009g0360 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.7+5366C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347845 | ||||||
| chr5:180348015
|
A | G | 64 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0001t0006g0374others(61): Show | 67 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.7+5196T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348015 | ||||||
| chr5:180348102
|
C | T | 63 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0001t0006g0374others(60): Show | 66 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.7+5109G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348102 | ||||||
| chr5:180348121
|
C | A | 4 | a0001c0001t0001g0208a0002c0002t0008g0012a0002c0002t0008g0247others(1): Show | 5 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+5090G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348121 | ||||||
| chr5:180348132
|
G | T | 1 | a0001c0005t0006g0380 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.7+5079C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348132 | ||||||
| chr5:180348221
|
C | T | 58 | a0001c0001t0001g0221a0001c0001t0006g0374a0001c0001t0006g0376others(55): Show | 59 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.7+4990G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348221 | ||||||
| chr5:180348370
|
T | C | 3 | a0001c0004t0030g0368a0001c0005t0017g0369a0001c0005t0017g0371 | 3 | HG02486.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.7+4841A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348370 | ||||||
| chr5:180348441
|
C | T | 14 | a0001c0001t0006g0378a0001c0001t0006g0385a0001c0001t0006g0386others(11): Show | 14 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.7+4770G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348441 | ||||||
| chr5:180348463
|
G | A | 5 | a0001c0001t0001g0208a0001c0004t0002g0013a0002c0002t0008g0012others(2): Show | 7 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+4748C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348463 | ||||||
| chr5:180348541
|
C | T | 1 | a0001c0004t0001g0171 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.7+4670G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348541 | ||||||
| chr5:180348634
|
C | T | 2 | a0001c0001t0002g0275a0001c0004t0002g0276 | 2 | HG01070.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.7+4577G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348634 | ||||||
| chr5:180348732
|
C | CT | 17 | a0001c0003t0001g0231a0001c0003t0002g0272a0001c0003t0002g0273others(14): Show | 17 | HG01975.hp1 HG02148.hp1 HG02735.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+4478dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348732 | ||||||
| chr5:180348732
|
CT | C | 60 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0001t0006g0374others(57): Show | 63 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.7+4478delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348732 | ||||||
| chr5:180348792
|
A | G | 2 | a0001c0005t0003g0107a0002c0002t0003g0106 | 2 | HG01358.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.7+4419T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348792 | ||||||
| chr5:180348888
|
C | T | 41 | a0001c0001t0001g0221a0001c0003t0001g0065a0001c0003t0001g0078others(38): Show | 42 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.7+4323G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348888 | ||||||
| chr5:180348898
|
C | T | 1 | a0001c0021t0002g0271 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7+4313G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348898 | ||||||
| chr5:180348976
|
G | A | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(106): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.7+4235C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348976 | ||||||
| chr5:180349036
|
G | A | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(106): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.7+4175C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349036 | ||||||
| chr5:180349135
|
A | G | 1 | a0001c0003t0002g0262 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.7+4076T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349135 | ||||||
| chr5:180349320
|
A | G | 1 | a0001c0004t0002g0365 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7+3891T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349320 | ||||||
| chr5:180349329
|
A | T | 1 | a0001c0004t0001g0056 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.7+3882T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349329 | ||||||
| chr5:180349365
|
A | C | 4 | a0001c0003t0001g0102a0002c0002t0003g0103a0002c0002t0003g0104others(1): Show | 4 | NA18981.hp1 NA18994.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+3846T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349365 | ||||||
| chr5:180349405
|
T | C | 3 | a0001c0004t0001g0205a0001c0004t0001g0206a0001c0005t0001g0207 | 3 | HG02630.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7+3806A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349405 | ||||||
| chr5:180349469
|
C | T | 1 | a0002c0015t0001g0009 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.7+3742G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349469 | ||||||
| chr5:180349496
|
T | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(90): Show | 99 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.7+3715A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349496 | ||||||
| chr5:180349514
|
T | A | 237 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(234): Show | 246 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.7+3697A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349514 | ||||||
| chr5:180349530
|
T | C | 3 | a0001c0001t0006g0376a0001c0004t0002g0258a0001c0004t0006g0375 | 3 | HG03098.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.7+3681A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349530 | ||||||
| chr5:180349561
|
C | T | 1 | a0001c0005t0027g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7+3650G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349561 | ||||||
| chr5:180349585
|
G | A | 30 | a0001c0001t0010g0038a0001c0001t0010g0049a0001c0003t0010g0028others(27): Show | 30 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.7+3626C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349585 | ||||||
| chr5:180349600
|
G | A | 1 | a0001c0003t0002g0361 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.7+3611C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349600 | ||||||
| chr5:180349750
|
G | A | 2 | a0001c0005t0006g0380a0001c0005t0031g0377 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.7+3461C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349750 | ||||||
| chr5:180349855
|
T | C | 3 | a0001c0004t0002g0258a0005c0010t0002g0256a0005c0010t0002g0257 | 3 | HG02965.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.7+3356A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349855 | ||||||
| chr5:180349878
|
GT | G | 50 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0001t0006g0374others(47): Show | 53 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.7+3332delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349878 | ||||||
| chr5:180349891
|
T | G | 3 | a0001c0001t0006g0374a0001c0001t0006g0376a0001c0004t0006g0375 | 3 | HG02809.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7+3320A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349891 | ||||||
| chr5:180349986
|
T | C | 1 | a0002c0002t0003g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.7+3225A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349986 | ||||||
| chr5:180350127
|
G | A | 13 | a0001c0001t0006g0378a0001c0001t0006g0381a0001c0001t0006g0385others(10): Show | 13 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.7+3084C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350127 | ||||||
| chr5:180350389
|
G | A | 2 | a0001c0003t0001g0085a0001c0003t0001g0086 | 2 | HG00673.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.7+2822C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350389 | ||||||
| chr5:180350517
|
G | A | 10 | a0002c0002t0003g0092a0002c0002t0003g0093a0002c0002t0003g0094others(7): Show | 10 | HG00438.hp1 HG00597.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.7+2694C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350517 | ||||||
| chr5:180350655
|
G | C | 1 | a0001c0003t0002g0363 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.7+2556C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350655 | ||||||
| chr5:180350687
|
AG | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(90): Show | 99 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.7+2523delC | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350687 | ||||||
| chr5:180350690
|
A | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(90): Show | 99 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.7+2521T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350690 | ||||||
| chr5:180350724
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.7+2487T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350724 | ||||||
| chr5:180350804
|
C | G | 1 | a0001c0004t0002g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.7+2407G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350804 | ||||||
| chr5:180350869
|
T | C | 11 | a0001c0001t0001g0219a0001c0003t0001g0209a0001c0003t0001g0218others(8): Show | 11 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.7+2342A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350869 | ||||||
| chr5:180350897
|
T | C | 1 | a0002c0007t0002g0364 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.7+2314A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350897 | ||||||
| chr5:180350964
|
C | T | 43 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0010g0038others(40): Show | 43 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.7+2247G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350964 | ||||||
| chr5:180351047
|
T | C | 1 | a0001c0003t0006g0387 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7+2164A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351047 | ||||||
| chr5:180351098
|
T | A | 60 | a0001c0001t0001g0221a0001c0001t0006g0374a0001c0001t0006g0376others(57): Show | 62 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.7+2113A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351098 | ||||||
| chr5:180351151
|
T | C | 1 | a0001c0005t0015g0366 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.7+2060A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351151 | ||||||
| chr5:180351366
|
C | G | 1 | a0002c0002t0007g0022 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.7+1845G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351366 | ||||||
| chr5:180351393
|
C | T | 1 | a0002c0015t0001g0009 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.7+1818G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351393 | ||||||
| chr5:180351423
|
C | T | 1 | a0001c0003t0002g0269 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.7+1788G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351423 | ||||||
| chr5:180351626
|
C | T | 3 | a0001c0004t0030g0368a0001c0005t0017g0369a0001c0005t0017g0371 | 3 | HG02486.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.7+1585G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351626 | ||||||
| chr5:180351738
|
G | A | 1 | a0001c0005t0004g0222 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.7+1473C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351738 | ||||||
| chr5:180351923
|
G | T | 1 | a0001c0004t0002g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.7+1288C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351923 | ||||||
| chr5:180352124
|
G | A | 13 | a0001c0003t0001g0231a0001c0004t0013g0052a0002c0002t0003g0053others(10): Show | 13 | HG01975.hp1 HG03239.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.7+1087C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352124 | ||||||
| chr5:180352206
|
G | C | 1 | a0001c0001t0001g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.7+1005C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352206 | ||||||
| chr5:180352293
|
C | A | 1 | a0001c0004t0002g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.7+918G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352293 | ||||||
| chr5:180352339
|
G | GA | 133 | a0001c0001t0001g0246a0001c0001t0002g0003a0001c0001t0002g0018others(130): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.7+871dupT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352339 | ||||||
| chr5:180352339
|
GA | G | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(86): Show | 95 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.7+871delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352339 | ||||||
| chr5:180352339
|
GAA | G | 38 | a0001c0001t0006g0374a0001c0003t0001g0065a0001c0003t0001g0078others(35): Show | 39 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.7+870_7+871delTT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352339 | ||||||
| chr5:180352340
|
A | G | 2 | a0002c0002t0003g0087a0003c0006t0012g0088 | 2 | NA18959.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.7+871T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352340 | ||||||
| chr5:180352341
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.7+870T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352341 | ||||||
| chr5:180352360
|
G | T | 1 | a0002c0002t0009g0255 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.7+851C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352360 | ||||||
| chr5:180352375
|
T | C | 1 | a0002c0002t0003g0249 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.7+836A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352375 | ||||||
| chr5:180352506
|
C | G | 1 | a0001c0005t0011g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.7+705G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352506 | ||||||
| chr5:180352607
|
G | C | 13 | a0001c0001t0006g0381a0001c0001t0006g0385a0001c0001t0006g0386others(10): Show | 13 | HG00280.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.7+604C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352607 | ||||||
| chr5:180352683
|
C | G | 1 | a0002c0002t0003g0053 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.7+528G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352683 | ||||||
| chr5:180352903
|
G | A | 2 | a0001c0001t0018g0372a0001c0001t0018g0373 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.7+308C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352903 | ||||||
| chr5:180352932
|
C | T | 1 | a0001c0003t0002g0253 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.7+279G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352932 | ||||||
| chr5:180352974
|
G | A | 1 | a0001c0003t0001g0250 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.7+237C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352974 | ||||||
| chr5:180353056
|
C | T | 1 | a0001c0003t0002g0252 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.7+155G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180353056 | ||||||
| chr5:180353104
|
C | G | 2 | a0001c0001t0018g0372a0001c0001t0018g0373 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.7+107G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180353104 | ||||||
| chr5:180353134
|
C | T | 1 | a0001c0004t0002g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.7+77G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180353134 | ||||||
| chr5:180353181
|
G | A | 1 | a0001c0009t0002g0367 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7+30C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180353181 |