Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 144195 |
|---|---|
| ensemblid | ENSG00000173262.12 |
| hgncid | 18301 |
| symbol | SLC2A14 |
| name | solute carrier family 2 member 14 |
| refseq_nuc | NM_001286234.2 |
| refseq_prot | NP_001273163.1 |
| ensembl_nuc | ENST00000431042.7 |
| ensembl_prot | ENSP00000407287.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 7812514 |
| end | 7872915 |
| strand | - |
| ver | v1.2 |
| region | chr12:7812514-7872915 |
| region5000 | chr12:7807514-7877915 |
| regionname0 | SLC2A14_chr12_7812514_7872915 |
| regionname5000 | SLC2A14_chr12_7807514_7877915 |
| 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 | 497 | 263 | 79 | 51 | 98 | 10 | 23 | 71 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0002 | 0/0 | 497 | 83 | 8 | 13 | 45 | 4 | 13 | 28 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0003 | 0/0 | 497 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0004 | 0/0 | 497 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0005 | 0/0 | 497 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| 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 | 0/0 | 1494 | 70 | 5 | 13 | 35 | 4 | 13 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0002 | 0/0 | 1494 | 61 | 3 | 25 | 19 | 6 | 8 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0003 | 0/0 | 1494 | 53 | 24 | 1 | 24 | 0 | 4 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0004 | 1/0 | 1494 | 51 | 24 | 15 | 0 | 4 | 7 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0005 | 0/1 | 1494 | 40 | 9 | 5 | 24 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0006 | 0/0 | 1494 | 25 | 10 | 4 | 11 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0007 | 0/0 | 1494 | 17 | 8 | 1 | 7 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0008 | 0/0 | 1494 | 15 | 0 | 0 | 13 | 0 | 2 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0009 | 0/0 | 1494 | 6 | 0 | 0 | 6 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0010 | 0/0 | 1494 | 4 | 0 | 0 | 4 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0011 | 0/0 | 1494 | 2 | 2 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0012 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0013 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0014 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0015 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0016 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| c0017 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| 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 | 0/0 | 1969 | 114 | 47 | 15 | 35 | 4 | 13 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0002 | 0/0 | 1969 | 81 | 5 | 13 | 46 | 4 | 13 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0003 | 0/0 | 1968 | 61 | 3 | 25 | 19 | 6 | 8 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0004 | 0/0 | 1969 | 30 | 6 | 5 | 18 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0005 | 0/1 | 1968 | 27 | 9 | 5 | 11 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0006 | 0/0 | 1968 | 12 | 0 | 0 | 12 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0007 | 0/0 | 1967 | 5 | 5 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0008 | 0/0 | 1969 | 4 | 4 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0009 | 0/0 | 1967 | 4 | 4 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0010 | 0/0 | 1969 | 3 | 2 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0011 | 0/0 | 1968 | 2 | 2 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0012 | 0/0 | 1969 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0013 | 1/0 | 1969 | 1 | 0 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0014 | 0/0 | 1969 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0015 | 0/0 | 1968 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0016 | 0/0 | 1969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0017 | 0/0 | 1969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| t0018 | 0/0 | 1969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| 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 | 2 | 0 | 1 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0345 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 1494 | 61 | 3 | 25 | 19 | 6 | 8 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0003 | 0/0 | 1494 | 53 | 24 | 1 | 24 | 0 | 4 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0004 | 1/0 | 1494 | 51 | 24 | 15 | 0 | 4 | 7 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0005 | 0/1 | 1494 | 40 | 9 | 5 | 24 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0006 | 0/0 | 1494 | 25 | 10 | 4 | 11 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0007 | 0/0 | 1494 | 17 | 8 | 1 | 7 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0008 | 0/0 | 1494 | 15 | 0 | 0 | 13 | 0 | 2 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0016 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0002c0001 | 0/0 | 1494 | 70 | 5 | 13 | 35 | 4 | 13 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0002c0009 | 0/0 | 1494 | 6 | 0 | 0 | 6 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0002c0010 | 0/0 | 1494 | 4 | 0 | 0 | 4 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0002c0011 | 0/0 | 1494 | 2 | 2 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0002c0013 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0003c0012 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0003c0014 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0004c0017 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0005c0015 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0003 | 0/0 | 3461 | 61 | 3 | 25 | 19 | 6 | 8 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0003t0001 | 0/0 | 3462 | 48 | 22 | 0 | 22 | 0 | 4 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0003t0010 | 0/0 | 3462 | 3 | 2 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0003t0012 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0003t0014 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0004t0001 | 0/0 | 3462 | 50 | 24 | 15 | 0 | 4 | 7 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0004t0013 | 1/0 | 3462 | 1 | 0 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0005t0005 | 0/1 | 3461 | 27 | 9 | 5 | 11 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0005t0006 | 0/0 | 3461 | 12 | 0 | 0 | 12 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0005t0015 | 0/0 | 3461 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0006t0004 | 0/0 | 3462 | 21 | 6 | 4 | 11 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0006t0009 | 0/0 | 3460 | 2 | 2 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0006t0016 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0006t0017 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0007t0004 | 0/0 | 3462 | 9 | 0 | 1 | 7 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0007t0007 | 0/0 | 3460 | 5 | 5 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0007t0009 | 0/0 | 3460 | 2 | 2 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0007t0018 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0008t0001 | 0/0 | 3462 | 15 | 0 | 0 | 13 | 0 | 2 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0001c0016t0008 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0002c0001t0001 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0002c0001t0002 | 0/0 | 3462 | 69 | 4 | 13 | 35 | 4 | 13 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0002c0009t0002 | 0/0 | 3462 | 6 | 0 | 0 | 6 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0002c0010t0002 | 0/0 | 3462 | 4 | 0 | 0 | 4 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0002c0011t0008 | 0/0 | 3462 | 2 | 2 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0002c0013t0002 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0003c0012t0011 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0003c0014t0011 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0004c0017t0002 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| a0005c0015t0008 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | copy fasta | chr12 | 7807514 | 7877915 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0002t0003g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0010g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0012g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0003t0014g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0004t0013g0345 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0006g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0006g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0005t0015g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0004g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0009g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0016g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0006t0017g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0007g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0009g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0007t0018g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0008t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0001c0016t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0009t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0009t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0009t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0009t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0009t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0009t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0010t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0010t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0010t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0010t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0011t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0011t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0002c0013t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0003c0012t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0003c0014t0011g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0004c0017t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| a0005c0015t0008g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0091 | EUR | GBR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0080 | EUR | GBR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00140 | hp1 | a0002 | c0001 | t0002 | g0064 | EUR | GBR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0090 | EUR | GBR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0347 | EUR | FIN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00280 | hp2 | a0001 | c0004 | t0001 | g0109 | EUR | FIN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00323 | hp1 | a0001 | c0004 | t0001 | g0197 | EUR | FIN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00323 | hp2 | a0002 | c0001 | t0002 | g0063 | EUR | FIN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00408 | hp1 | a0001 | c0005 | t0006 | g0167 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00408 | hp2 | a0002 | c0009 | t0002 | g0072 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0044 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00423 | hp2 | a0002 | c0001 | t0002 | g0150 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00438 | hp1 | a0002 | c0001 | t0002 | g0149 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00438 | hp2 | a0002 | c0001 | t0002 | g0250 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00544 | hp1 | a0001 | c0006 | t0004 | g0161 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00544 | hp2 | a0002 | c0001 | t0002 | g0101 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00597 | hp1 | a0002 | c0001 | t0002 | g0241 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00597 | hp2 | a0002 | c0001 | t0002 | g0214 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0225 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00609 | hp2 | a0001 | c0006 | t0004 | g0220 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00621 | hp1 | a0001 | c0005 | t0005 | g0033 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00621 | hp2 | a0002 | c0001 | t0002 | g0163 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0096 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00639 | hp2 | a0001 | c0004 | t0001 | g0348 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0337 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0092 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00673 | hp1 | a0001 | c0008 | t0001 | g0201 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00673 | hp2 | a0001 | c0005 | t0005 | g0120 | EAS | CHS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0159 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00735 | hp2 | a0001 | c0004 | t0001 | g0306 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00738 | hp1 | a0001 | c0004 | t0001 | g0248 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0126 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0262 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0111 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01074 | hp1 | a0001 | c0005 | t0005 | g0140 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0260 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0125 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01081 | hp2 | a0002 | c0001 | t0002 | g0001 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01099 | hp1 | a0002 | c0001 | t0002 | g0265 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01099 | hp2 | a0001 | c0004 | t0001 | g0294 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0075 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0147 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0016 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0076 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01167 | hp1 | a0002 | c0001 | t0002 | g0261 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01167 | hp2 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01168 | hp1 | a0001 | c0005 | t0005 | g0334 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01168 | hp2 | a0001 | c0004 | t0001 | g0296 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01169 | hp1 | a0001 | c0004 | t0001 | g0297 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01175 | hp1 | a0002 | c0001 | t0002 | g0174 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0093 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0293 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01192 | hp2 | a0001 | c0004 | t0001 | g0312 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01243 | hp1 | a0001 | c0005 | t0005 | g0323 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0071 | AMR | PUR | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0132 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0257 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01256 | hp1 | a0002 | c0001 | t0002 | g0295 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0302 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01257 | hp1 | a0002 | c0001 | t0002 | g0168 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01257 | hp2 | a0001 | c0004 | t0001 | g0097 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0134 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0128 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01346 | hp1 | a0002 | c0001 | t0002 | g0070 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01346 | hp2 | a0001 | c0007 | t0004 | g0146 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0142 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0121 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01496 | hp1 | a0001 | c0005 | t0005 | g0338 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01496 | hp2 | a0001 | c0006 | t0004 | g0137 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0258 | EUR | IBS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01517 | hp2 | a0001 | c0004 | t0001 | g0195 | EUR | IBS | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01884 | hp1 | a0003 | c0014 | t0011 | g0102 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01884 | hp2 | a0002 | c0001 | t0002 | g0012 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0328 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01928 | hp1 | a0001 | c0002 | t0003 | g0119 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01928 | hp2 | a0002 | c0001 | t0002 | g0325 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0085 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01934 | hp2 | a0002 | c0001 | t0002 | g0180 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01943 | hp1 | a0001 | c0006 | t0004 | g0073 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01943 | hp2 | a0002 | c0001 | t0002 | g0321 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01952 | hp1 | a0001 | c0003 | t0010 | g0098 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0021 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01981 | hp1 | a0001 | c0006 | t0004 | g0035 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01981 | hp2 | a0002 | c0001 | t0002 | g0074 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0259 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01993 | hp2 | a0001 | c0006 | t0004 | g0349 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0020 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02004 | hp2 | a0002 | c0001 | t0002 | g0322 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02015 | hp1 | a0002 | c0001 | t0002 | g0151 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02015 | hp2 | a0001 | c0002 | t0003 | g0094 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02027 | hp1 | a0001 | c0003 | t0001 | g0083 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02027 | hp2 | a0002 | c0001 | t0002 | g0030 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02040 | hp1 | a0002 | c0001 | t0002 | g0065 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02040 | hp2 | a0001 | c0006 | t0004 | g0324 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0191 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0017 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0256 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02056 | hp2 | a0001 | c0005 | t0006 | g0175 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02074 | hp1 | a0001 | c0005 | t0006 | g0005 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02074 | hp2 | a0002 | c0001 | t0002 | g0032 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02080 | hp1 | a0001 | c0005 | t0005 | g0061 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0095 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02083 | hp2 | a0001 | c0008 | t0001 | g0240 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02129 | hp1 | a0001 | c0005 | t0005 | g0039 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0116 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02132 | hp1 | a0002 | c0001 | t0002 | g0040 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02132 | hp2 | a0001 | c0005 | t0006 | g0165 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02135 | hp1 | a0001 | c0008 | t0001 | g0025 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02135 | hp2 | a0001 | c0005 | t0005 | g0205 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0190 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02145 | hp2 | a0001 | c0006 | t0004 | g0157 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02155 | hp1 | a0001 | c0003 | t0014 | g0139 | EAS | CDX | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02155 | hp2 | a0002 | c0009 | t0002 | g0026 | EAS | CDX | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0069 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02257 | hp2 | a0001 | c0006 | t0009 | g0081 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02258 | hp1 | a0001 | c0005 | t0005 | g0193 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02258 | hp2 | a0001 | c0005 | t0005 | g0114 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02273 | hp1 | a0002 | c0001 | t0002 | g0223 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0122 | AMR | PEL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02280 | hp1 | a0001 | c0004 | t0001 | g0009 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02280 | hp2 | a0005 | c0015 | t0008 | g0341 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0192 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02451 | hp2 | a0001 | c0005 | t0005 | g0008 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02523 | hp1 | a0001 | c0006 | t0004 | g0046 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02523 | hp2 | a0002 | c0010 | t0002 | g0243 | EAS | KHV | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02572 | hp1 | a0001 | c0005 | t0005 | g0327 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0186 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02602 | hp1 | a0001 | c0004 | t0001 | g0267 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0141 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0326 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02615 | hp2 | a0002 | c0011 | t0008 | g0003 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0314 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0290 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0254 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02630 | hp2 | a0001 | c0016 | t0008 | g0152 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02647 | hp1 | a0001 | c0004 | t0001 | g0183 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0330 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0344 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0188 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02723 | hp1 | a0001 | c0003 | t0010 | g0013 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0272 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0298 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0105 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0066 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02738 | hp2 | a0001 | c0004 | t0001 | g0171 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0187 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02818 | hp2 | a0001 | c0005 | t0005 | g0255 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02886 | hp1 | a0001 | c0007 | t0009 | g0291 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02886 | hp2 | a0001 | c0005 | t0005 | g0342 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02895 | hp1 | a0001 | c0006 | t0004 | g0115 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02895 | hp2 | a0001 | c0007 | t0007 | g0211 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02896 | hp1 | a0001 | c0007 | t0007 | g0234 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0135 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02897 | hp2 | a0001 | c0007 | t0007 | g0209 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02922 | hp1 | a0001 | c0005 | t0005 | g0340 | AFR | ESN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02922 | hp2 | a0001 | c0007 | t0018 | g0346 | AFR | ESN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02965 | hp1 | a0002 | c0001 | t0001 | g0232 | AFR | ESN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02965 | hp2 | a0001 | c0006 | t0004 | g0288 | AFR | ESN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02970 | hp1 | a0001 | c0006 | t0004 | g0158 | AFR | ESN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0266 | AFR | ESN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03017 | hp1 | a0002 | c0001 | t0002 | g0253 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03017 | hp2 | a0002 | c0001 | t0002 | g0179 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03041 | hp1 | a0001 | c0006 | t0017 | g0181 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03041 | hp2 | a0001 | c0004 | t0001 | g0285 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0011 | AFR | MSL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03098 | hp2 | a0001 | c0007 | t0009 | g0078 | AFR | MSL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03130 | hp1 | a0001 | c0002 | t0003 | g0108 | AFR | ESN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03130 | hp2 | a0002 | c0013 | t0002 | g0182 | AFR | ESN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03139 | hp1 | a0001 | c0004 | t0001 | g0332 | AFR | ESN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0189 | AFR | ESN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0117 | AFR | ESN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0331 | AFR | ESN | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0320 | AFR | MSL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0333 | AFR | MSL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0316 | AFR | MSL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0315 | AFR | MSL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0236 | AFR | MSL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03486 | hp2 | a0003 | c0012 | t0011 | g0113 | AFR | MSL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0144 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03491 | hp2 | a0002 | c0001 | t0002 | g0245 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0176 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0206 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0184 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0237 | AFR | GWD | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0318 | AFR | MSL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03579 | hp2 | a0001 | c0006 | t0004 | g0286 | AFR | MSL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03654 | hp1 | a0001 | c0002 | t0003 | g0082 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03654 | hp2 | a0002 | c0001 | t0002 | g0309 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03669 | hp1 | a0002 | c0001 | t0002 | g0305 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0303 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03688 | hp1 | a0002 | c0001 | t0002 | g0228 | SAS | STU | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03688 | hp2 | a0001 | c0005 | t0005 | g0172 | SAS | STU | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03704 | hp1 | a0001 | c0004 | t0001 | g0106 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03704 | hp2 | a0001 | c0007 | t0004 | g0275 | SAS | PJL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0107 | SAS | BEB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0047 | SAS | BEB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03834 | hp1 | a0002 | c0001 | t0002 | g0299 | SAS | BEB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03834 | hp2 | a0001 | c0008 | t0001 | g0154 | SAS | BEB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03942 | hp1 | a0002 | c0001 | t0002 | g0276 | SAS | BEB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03942 | hp2 | a0001 | c0004 | t0001 | g0118 | SAS | BEB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG04115 | hp1 | a0002 | c0001 | t0002 | g0301 | SAS | STU | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG04115 | hp2 | a0001 | c0008 | t0001 | g0274 | SAS | STU | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG04184 | hp1 | a0002 | c0001 | t0002 | g0300 | SAS | BEB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG04184 | hp2 | a0001 | c0004 | t0001 | g0198 | SAS | BEB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0308 | SAS | STU | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG04199 | hp2 | a0002 | c0001 | t0002 | g0036 | SAS | STU | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG04228 | hp1 | a0001 | c0004 | t0001 | g0110 | SAS | STU | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG04228 | hp2 | a0002 | c0001 | t0002 | g0227 | SAS | STU | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18522 | hp1 | a0001 | c0006 | t0004 | g0287 | AFR | YRI | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0339 | AFR | YRI | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18612 | hp1 | a0001 | c0008 | t0001 | g0084 | EAS | CHB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18612 | hp2 | a0002 | c0009 | t0002 | g0264 | EAS | CHB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18747 | hp1 | a0002 | c0001 | t0002 | g0210 | EAS | CHB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18747 | hp2 | a0001 | c0007 | t0004 | g0019 | EAS | CHB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18906 | hp1 | a0001 | c0006 | t0009 | g0284 | AFR | YRI | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0127 | AFR | YRI | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18941 | hp2 | a0001 | c0005 | t0015 | g0029 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18944 | hp1 | a0004 | c0017 | t0002 | g0129 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18944 | hp2 | a0002 | c0001 | t0002 | g0310 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18945 | hp2 | a0001 | c0007 | t0004 | g0281 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18947 | hp1 | a0001 | c0005 | t0005 | g0062 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18947 | hp2 | a0001 | c0006 | t0004 | g0246 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18948 | hp1 | a0002 | c0001 | t0002 | g0131 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18948 | hp2 | a0001 | c0006 | t0004 | g0051 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18949 | hp1 | a0001 | c0002 | t0003 | g0054 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18949 | hp2 | a0001 | c0008 | t0001 | g0242 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18952 | hp1 | a0001 | c0008 | t0001 | g0023 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18952 | hp2 | a0002 | c0001 | t0002 | g0202 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18953 | hp1 | a0001 | c0006 | t0004 | g0207 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18953 | hp2 | a0001 | c0005 | t0005 | g0229 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18954 | hp1 | a0002 | c0001 | t0002 | g0231 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18954 | hp2 | a0001 | c0008 | t0001 | g0238 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18959 | hp1 | a0002 | c0001 | t0002 | g0086 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18959 | hp2 | a0001 | c0007 | t0004 | g0043 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18962 | hp1 | a0001 | c0007 | t0004 | g0204 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18969 | hp1 | a0001 | c0005 | t0005 | g0213 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18969 | hp2 | a0001 | c0008 | t0001 | g0045 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0058 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18970 | hp2 | a0001 | c0005 | t0005 | g0249 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18975 | hp1 | a0002 | c0001 | t0002 | g0247 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0283 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18977 | hp1 | a0002 | c0010 | t0002 | g0138 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18977 | hp2 | a0002 | c0001 | t0002 | g0177 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0263 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18980 | hp2 | a0001 | c0006 | t0004 | g0038 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18981 | hp1 | a0001 | c0002 | t0003 | g0087 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18981 | hp2 | a0001 | c0005 | t0006 | g0178 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0226 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18983 | hp1 | a0002 | c0009 | t0002 | g0052 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18983 | hp2 | a0001 | c0005 | t0006 | g0059 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18984 | hp1 | a0002 | c0010 | t0002 | g0049 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18988 | hp1 | a0001 | c0008 | t0001 | g0200 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18988 | hp2 | a0002 | c0001 | t0002 | g0156 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18989 | hp1 | a0001 | c0008 | t0001 | g0099 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18989 | hp2 | a0001 | c0006 | t0004 | g0233 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18990 | hp1 | a0002 | c0001 | t0002 | g0155 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18990 | hp2 | a0002 | c0001 | t0002 | g0162 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18995 | hp2 | a0002 | c0001 | t0002 | g0208 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18999 | hp1 | a0001 | c0005 | t0005 | g0282 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18999 | hp2 | a0002 | c0001 | t0002 | g0215 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0244 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19000 | hp2 | a0002 | c0001 | t0002 | g0160 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19002 | hp1 | a0001 | c0005 | t0005 | g0224 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19004 | hp1 | a0001 | c0007 | t0004 | g0203 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19004 | hp2 | a0001 | c0005 | t0006 | g0169 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19010 | hp1 | a0002 | c0001 | t0002 | g0216 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19010 | hp2 | a0002 | c0001 | t0002 | g0199 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0343 | AFR | LWK | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0329 | AFR | LWK | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19043 | hp1 | a0001 | c0003 | t0010 | g0014 | AFR | LWK | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0007 | AFR | LWK | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19054 | hp1 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19054 | hp2 | a0002 | c0001 | t0002 | g0088 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19055 | hp1 | a0001 | c0008 | t0001 | g0048 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19055 | hp2 | a0001 | c0005 | t0006 | g0034 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19058 | hp1 | a0002 | c0001 | t0002 | g0037 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19058 | hp2 | a0001 | c0007 | t0004 | g0230 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19064 | hp1 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19064 | hp2 | a0001 | c0005 | t0006 | g0166 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19065 | hp2 | a0001 | c0005 | t0006 | g0252 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19066 | hp1 | a0001 | c0005 | t0006 | g0006 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19066 | hp2 | a0002 | c0001 | t0002 | g0311 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19067 | hp1 | a0001 | c0002 | t0003 | g0148 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19067 | hp2 | a0001 | c0003 | t0001 | g0067 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19070 | hp1 | a0002 | c0009 | t0002 | g0143 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19072 | hp1 | a0002 | c0001 | t0002 | g0133 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19072 | hp2 | a0001 | c0002 | t0003 | g0278 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19074 | hp1 | a0001 | c0006 | t0004 | g0212 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19074 | hp2 | a0001 | c0008 | t0001 | g0004 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19079 | hp1 | a0002 | c0010 | t0002 | g0050 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19079 | hp2 | a0002 | c0001 | t0002 | g0217 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19081 | hp1 | a0001 | c0003 | t0012 | g0057 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0280 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19084 | hp1 | a0002 | c0009 | t0002 | g0103 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19085 | hp1 | a0001 | c0003 | t0001 | g0219 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19085 | hp2 | a0002 | c0001 | t0002 | g0194 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19086 | hp1 | a0002 | c0001 | t0002 | g0251 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19086 | hp2 | a0001 | c0006 | t0004 | g0164 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19087 | hp1 | a0001 | c0005 | t0006 | g0170 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19089 | hp1 | a0001 | c0002 | t0003 | g0100 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19089 | hp2 | a0001 | c0002 | t0003 | g0055 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19090 | hp1 | a0001 | c0007 | t0004 | g0027 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0279 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19091 | hp1 | a0001 | c0008 | t0001 | g0239 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0277 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19240 | hp1 | a0001 | c0006 | t0016 | g0273 | AFR | YRI | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA19240 | hp2 | a0001 | c0007 | t0007 | g0235 | AFR | YRI | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA20129 | hp1 | a0001 | c0005 | t0005 | g0319 | AFR | ASW | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA20129 | hp2 | a0002 | c0011 | t0008 | g0289 | AFR | ASW | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA20752 | hp1 | a0001 | c0004 | t0001 | g0123 | EUR | TSI | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0292 | EUR | TSI | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA20805 | hp1 | a0002 | c0001 | t0002 | g0001 | EUR | TSI | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA20805 | hp2 | a0002 | c0001 | t0002 | g0104 | EUR | TSI | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0304 | SAS | GIH | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA20905 | hp2 | a0002 | c0001 | t0002 | g0124 | SAS | GIH | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01123 | hp1 | a0001 | c0004 | t0001 | g0307 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG01123 | hp2 | a0001 | c0005 | t0005 | g0336 | AMR | CLM | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02486 | hp1 | a0001 | c0007 | t0007 | g0269 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02486 | hp2 | a0002 | c0001 | t0002 | g0270 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02559 | hp1 | a0001 | c0005 | t0005 | g0335 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0313 | AFR | ACB | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03471 | hp1 | a0002 | c0001 | t0002 | g0002 | AFR | MSL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0112 | AFR | MSL | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0079 | AFR | USA | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0185 | AFR | USA | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18955 | hp1 | a0001 | c0003 | t0001 | g0153 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0053 | EAS | JPT | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA20300 | hp1 | a0001 | c0002 | t0003 | g0022 | AFR | USA | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA20300 | hp2 | a0002 | c0001 | t0002 | g0271 | AFR | USA | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0268 | AFR | LWK | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0317 | AFR | LWK | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0005 | t0005 | g0173 | REF | REF | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0013 | g0345 | REF | REF | SLC2A14_chr12_7807514_7877915 | SLC2A14 | chr12 | 7807514 | 7877915 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7814362
|
C | T | 3 | a0002a0004a0005 | 85 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
missense_variant | MODERATE | c.1448G>A | p.Gly483Glu | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1614/3462 | 1448/1494 | 483/497 | chr12 | 7814362 | ||
| chr12:7814534
|
A | G | 2 | a0003a0005 | 3 | HG01884.hp1 HG02280.hp2 HG03486.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1276T>C | p.Tyr426His | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1442/3462 | 1276/1494 | 426/497 | chr12 | 7814534 | ||
| chr12:7831742
|
T | A | 1 | a0004 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.134A>T | p.Lys45Ile | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/11 | 300/3462 | 134/1494 | 45/497 | chr12 | 7831742 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7814379
|
C | T | 2 | a0001c0002a0001c0005 | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(98): Show |
synonymous_variant | LOW | c.1431G>A | p.Gly477Gly | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1597/3462 | 1431/1494 | 477/497 | chr12 | 7814379 | ||
| chr12:7814475
|
G | A | 6 | a0001c0006a0001c0007a0001c0008others(3): Show | 61 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(58): Show |
synonymous_variant | LOW | c.1335C>T | p.Ala445Ala | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1501/3462 | 1335/1494 | 445/497 | chr12 | 7814475 | ||
| chr12:7814480
|
A | G | 1 | a0001c0002 | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(58): Show |
synonymous_variant | LOW | c.1330T>C | p.Leu444Leu | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1496/3462 | 1330/1494 | 444/497 | chr12 | 7814480 | ||
| chr12:7814499
|
G | A | 1 | a0001c0008 | 15 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(12): Show |
synonymous_variant | LOW | c.1311C>T | p.Thr437Thr | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1477/3462 | 1311/1494 | 437/497 | chr12 | 7814499 | ||
| chr12:7817861
|
G | A | 1 | a0001c0016 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.1245C>T | p.Phe415Phe | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/11 | 1411/3462 | 1245/1494 | 415/497 | chr12 | 7817861 | ||
| chr12:7817957
|
G | A | 1 | a0002c0010 | 4 | HG02523.hp2 NA18977.hp1 NA18984.hp1 others(1): Show |
synonymous_variant | LOW | c.1149C>T | p.Gly383Gly | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/11 | 1315/3462 | 1149/1494 | 383/497 | chr12 | 7817957 | ||
| chr12:7827582
|
C | T | 4 | a0001c0003a0001c0006a0002c0013others(1): Show | 80 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(77): Show |
synonymous_variant | LOW | c.777G>A | p.Leu259Leu | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/11 | 943/3462 | 777/1494 | 259/497 | chr12 | 7827582 | ||
| chr12:7828822
|
C | A | 2 | a0002c0009a0002c0010 | 10 | HG00408.hp2 HG02155.hp2 HG02523.hp2 others(7): Show |
synonymous_variant | LOW | c.558G>T | p.Pro186Pro | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/11 | 724/3462 | 558/1494 | 186/497 | chr12 | 7828822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7812753
|
G | A | 1 | a0001c0007t0007 | 5 | HG02486.hp1 HG02895.hp2 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1563C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1563 | chr12 | 7812753 | |||||
| chr12:7812898
|
A | G | 1 | a0001c0003t0010 | 3 | HG01952.hp1 HG02723.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1418T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1418 | chr12 | 7812898 | |||||
| chr12:7812910
|
A | C | 2 | a0001c0005t0006a0001c0005t0015 | 13 | HG00408.hp1 HG02056.hp2 HG02074.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1406T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1406 | chr12 | 7812910 | |||||
| chr12:7813072
|
G | A | 2 | a0003c0012t0011a0003c0014t0011 | 2 | HG01884.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1244C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1244 | chr12 | 7813072 | |||||
| chr12:7813104
|
T | C | 1 | a0001c0005t0015 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1212A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1212 | chr12 | 7813104 | |||||
| chr12:7813161
|
G | A | 29 | a0001c0002t0003a0001c0003t0001a0001c0003t0010others(26): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*1155C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1155 | chr12 | 7813161 | |||||
| chr12:7813206
|
A | C | 5 | a0002c0001t0002a0002c0009t0002a0002c0010t0002others(2): Show | 81 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1110T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1110 | chr12 | 7813206 | |||||
| chr12:7813295
|
T | C | 1 | a0001c0006t0017 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1021A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 1021 | chr12 | 7813295 | |||||
| chr12:7813585
|
AAG | A | 3 | a0001c0006t0009a0001c0007t0007a0001c0007t0009 | 9 | HG02257.hp2 HG02486.hp1 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*729_*730delCT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 729 | chr12 | 7813585 | |||||
| chr12:7813593
|
C | T | 13 | a0001c0002t0003a0001c0005t0005a0001c0005t0006others(10): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*723G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 723 | chr12 | 7813593 | |||||
| chr12:7813777
|
T | G | 13 | a0001c0002t0003a0001c0005t0005a0001c0005t0006others(10): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*539A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 539 | chr12 | 7813777 | |||||
| chr12:7813909
|
A | C | 18 | a0001c0002t0003a0001c0003t0014a0001c0005t0005others(15): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*407T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 407 | chr12 | 7813909 | |||||
| chr12:7813915
|
C | T | 18 | a0001c0002t0003a0001c0003t0014a0001c0005t0005others(15): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*401G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 401 | chr12 | 7813915 | |||||
| chr12:7813917
|
G | C | 18 | a0001c0002t0003a0001c0003t0014a0001c0005t0005others(15): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*399C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 399 | chr12 | 7813917 | |||||
| chr12:7813930
|
T | C | 18 | a0001c0002t0003a0001c0003t0014a0001c0005t0005others(15): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*386A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 386 | chr12 | 7813930 | |||||
| chr12:7813997
|
T | C | 17 | a0001c0002t0003a0001c0005t0005a0001c0005t0006others(14): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*319A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 319 | chr12 | 7813997 | |||||
| chr12:7814004
|
C | T | 7 | a0001c0002t0003a0001c0006t0009a0001c0007t0007others(4): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*312G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 312 | chr12 | 7814004 | |||||
| chr12:7814137
|
A | C | 1 | a0001c0003t0012 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*179T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 179 | chr12 | 7814137 | |||||
| chr12:7814162
|
T | C | 10 | a0001c0006t0004a0001c0006t0009a0001c0006t0017others(7): Show | 45 | HG00544.hp1 HG00609.hp2 HG01346.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*154A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 154 | chr12 | 7814162 | |||||
| chr12:7814227
|
CA | C | 6 | a0001c0002t0003a0001c0005t0005a0001c0005t0006others(3): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*88delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 88 | chr12 | 7814227 | |||||
| chr12:7814248
|
A | G | 3 | a0001c0002t0003a0003c0012t0011a0003c0014t0011 | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*68T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 68 | chr12 | 7814248 | |||||
| chr12:7814250
|
A | G | 3 | a0001c0002t0003a0003c0012t0011a0003c0014t0011 | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*66T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 66 | chr12 | 7814250 | |||||
| chr12:7814312
|
T | C | 17 | a0001c0002t0003a0001c0005t0005a0001c0005t0006others(14): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*4A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 11/11 | 4 | chr12 | 7814312 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7814539
|
T | A | 104 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
splice_region_variant&intron_variant | LOW | c.1276-5A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7814539 | ||||||
| chr12:7814752
|
A | G | 1 | a0001c0003t0001g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1276-218T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7814752 | ||||||
| chr12:7814796
|
T | G | 5 | a0001c0004t0001g0010a0001c0004t0001g0015a0001c0004t0001g0016others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276-262A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7814796 | ||||||
| chr12:7814825
|
A | T | 46 | a0001c0006t0004g0035a0001c0006t0004g0038a0001c0006t0004g0046others(43): Show | 46 | HG00544.hp1 HG00609.hp2 HG01346.hp2 others(43): Show |
intron_variant | MODIFIER | c.1276-291T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7814825 | ||||||
| chr12:7814926
|
A | G | 3 | a0002c0011t0008g0003a0002c0011t0008g0289a0005c0015t0008g0341 | 3 | HG02280.hp2 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1276-392T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7814926 | ||||||
| chr12:7814944
|
T | C | 118 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.1276-410A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7814944 | ||||||
| chr12:7815067
|
G | A | 15 | a0001c0008t0001g0004a0001c0008t0001g0023a0001c0008t0001g0025others(12): Show | 15 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.1276-533C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815067 | ||||||
| chr12:7815221
|
G | A | 1 | a0001c0002t0003g0280 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1276-687C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815221 | ||||||
| chr12:7815240
|
G | A | 15 | a0001c0008t0001g0004a0001c0008t0001g0023a0001c0008t0001g0025others(12): Show | 15 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.1276-706C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815240 | ||||||
| chr12:7815256
|
C | CA | 8 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(5): Show | 8 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-723dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815256 | ||||||
| chr12:7815291
|
C | T | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-757G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815291 | ||||||
| chr12:7815410
|
C | T | 80 | a0001c0003t0001g0317a0002c0001t0002g0001a0002c0001t0002g0002others(77): Show | 81 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1276-876G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815410 | ||||||
| chr12:7815448
|
C | T | 1 | a0001c0005t0005g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1276-914G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815448 | ||||||
| chr12:7815516
|
T | C | 267 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1276-982A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815516 | ||||||
| chr12:7815539
|
G | A | 303 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1276-1005C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815539 | ||||||
| chr12:7815550
|
C | T | 6 | a0001c0007t0007g0209a0001c0007t0007g0211a0001c0007t0007g0234others(3): Show | 6 | HG02486.hp1 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-1016G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815550 | ||||||
| chr12:7815556
|
T | C | 1 | a0001c0003t0001g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1276-1022A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815556 | ||||||
| chr12:7815570
|
G | A | 1 | a0001c0004t0001g0339 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1276-1036C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815570 | ||||||
| chr12:7815590
|
T | G | 24 | a0001c0006t0004g0035a0001c0006t0004g0038a0001c0006t0004g0046others(21): Show | 24 | HG00544.hp1 HG00609.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.1276-1056A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815590 | ||||||
| chr12:7815601
|
A | T | 148 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(145): Show | 149 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1276-1067T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815601 | ||||||
| chr12:7815618
|
C | T | 155 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(152): Show | 156 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1276-1084G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815618 | ||||||
| chr12:7815634
|
T | C | 2 | a0002c0011t0008g0003a0002c0011t0008g0289 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1276-1100A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815634 | ||||||
| chr12:7815709
|
T | C | 152 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(149): Show | 153 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1276-1175A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815709 | ||||||
| chr12:7815722
|
A | G | 3 | a0001c0003t0001g0077a0001c0003t0001g0190a0001c0003t0001g0191 | 3 | HG01891.hp2 HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1276-1188T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815722 | ||||||
| chr12:7815822
|
C | T | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-1288G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815822 | ||||||
| chr12:7815845
|
G | C | 1 | a0001c0004t0001g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1276-1311C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815845 | ||||||
| chr12:7815882
|
G | GT | 152 | a0001c0002t0003g0132a0001c0003t0001g0018a0001c0003t0001g0024others(149): Show | 153 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1276-1349dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815882 | ||||||
| chr12:7815887
|
T | C | 1 | a0001c0004t0001g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1276-1353A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815887 | ||||||
| chr12:7815894
|
T | G | 33 | a0001c0004t0001g0011a0001c0004t0001g0069a0001c0004t0001g0071others(30): Show | 33 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1276-1360A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815894 | ||||||
| chr12:7815894
|
T | TTTTTTG | 37 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(34): Show | 37 | HG00609.hp1 HG01891.hp2 HG02027.hp1 others(34): Show |
intron_variant | MODIFIER | c.1276-1366_1276-136 others(10): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815894 | ||||||
| chr12:7815922
|
T | C | 2 | a0001c0003t0001g0314a0002c0013t0002g0182 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1276-1388A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7815922 | ||||||
| chr12:7816066
|
AATTTCTT others(330): Show |
A | 188 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1275+1428_1276-153 others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816066 | ||||||
| chr12:7816087
|
T | TA | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-1554_1276-155 others(5): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816087 | ||||||
| chr12:7816089
|
A | T | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-1555T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816089 | ||||||
| chr12:7816091
|
T | A | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-1557A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816091 | ||||||
| chr12:7816092
|
T | A | 5 | a0001c0004t0001g0069a0001c0004t0001g0110a0001c0004t0001g0118others(2): Show | 5 | HG00639.hp2 HG00735.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276-1558A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816092 | ||||||
| chr12:7816097
|
T | A | 1 | a0002c0001t0002g0265 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1276-1563A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816097 | ||||||
| chr12:7816098
|
A | T | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-1564T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816098 | ||||||
| chr12:7816101
|
T | C | 3 | a0002c0001t0002g0012a0002c0001t0002g0270a0002c0001t0002g0271 | 3 | HG01884.hp2 HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1276-1567A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816101 | ||||||
| chr12:7816102
|
T | A | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-1568A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816102 | ||||||
| chr12:7816107
|
A | T | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-1573T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816107 | ||||||
| chr12:7816142
|
G | A | 5 | a0002c0001t0002g0156a0002c0001t0002g0160a0002c0001t0002g0216others(2): Show | 5 | NA18954.hp1 NA18988.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276-1608C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816142 | ||||||
| chr12:7816472
|
C | T | 1 | a0001c0003t0001g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1275+1359G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816472 | ||||||
| chr12:7816473
|
A | G | 340 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1275+1358T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816473 | ||||||
| chr12:7816473
|
A | T | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275+1358T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816473 | ||||||
| chr12:7816475
|
G | A | 188 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1275+1356C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816475 | ||||||
| chr12:7816533
|
A | G | 1 | a0001c0002t0003g0100 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1275+1298T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816533 | ||||||
| chr12:7816600
|
C | A | 347 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1275+1231G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816600 | ||||||
| chr12:7816681
|
T | A | 1 | a0003c0014t0011g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1275+1150A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816681 | ||||||
| chr12:7816783
|
C | T | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275+1048G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816783 | ||||||
| chr12:7816884
|
G | T | 266 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1275+947C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816884 | ||||||
| chr12:7816939
|
G | T | 232 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1275+892C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816939 | ||||||
| chr12:7816976
|
G | A | 1 | a0001c0004t0001g0333 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1275+855C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7816976 | ||||||
| chr12:7817327
|
G | C | 115 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1275+504C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817327 | ||||||
| chr12:7817370
|
C | T | 1 | a0001c0003t0001g0024 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1275+461G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817370 | ||||||
| chr12:7817372
|
C | T | 1 | a0001c0003t0001g0190 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1275+459G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817372 | ||||||
| chr12:7817397
|
G | A | 1 | a0002c0011t0008g0289 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1275+434C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817397 | ||||||
| chr12:7817407
|
G | A | 22 | a0001c0003t0001g0117a0001c0003t0001g0135a0001c0003t0001g0136others(19): Show | 22 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1275+424C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817407 | ||||||
| chr12:7817495
|
A | G | 2 | a0001c0003t0001g0314a0002c0013t0002g0182 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1275+336T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817495 | ||||||
| chr12:7817627
|
C | T | 1 | a0001c0006t0016g0273 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1275+204G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817627 | ||||||
| chr12:7817628
|
A | G | 231 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1275+203T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817628 | ||||||
| chr12:7817681
|
C | T | 1 | a0002c0010t0002g0243 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1275+150G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817681 | ||||||
| chr12:7817739
|
A | AAAATATA others(1): Show |
36 | a0001c0002t0003g0080a0001c0002t0003g0082a0001c0002t0003g0094others(33): Show | 36 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1275+91_1275+92ins others(8): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817739 | ||||||
| chr12:7817739
|
A | AAAATATA others(5): Show |
113 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0031others(110): Show | 113 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.1275+91_1275+92ins others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817739 | ||||||
| chr12:7817739
|
A | AAAATATA others(9): Show |
38 | a0001c0002t0003g0020a0001c0002t0003g0044a0001c0002t0003g0053others(35): Show | 38 | HG00280.hp1 HG00423.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1275+91_1275+92ins others(16): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817739 | ||||||
| chr12:7817739
|
A | AAAATATA others(13): Show |
3 | a0001c0002t0003g0196a0001c0003t0010g0098a0001c0005t0005g0008 | 3 | HG01952.hp1 HG02451.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1275+91_1275+92ins others(20): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817739 | ||||||
| chr12:7817739
|
A | AAATATAG others(4): Show |
1 | a0001c0002t0003g0091 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1275+91_1275+92ins others(11): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817739 | ||||||
| chr12:7817739
|
A | AAATATAG others(8): Show |
1 | a0001c0003t0001g0083 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1275+91_1275+92ins others(15): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817739 | ||||||
| chr12:7817739
|
AATAT | A | 15 | a0001c0005t0005g0327a0001c0006t0004g0038a0001c0006t0004g0046others(12): Show | 15 | HG00609.hp2 HG02040.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1275+88_1275+91del others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817739 | ||||||
| chr12:7817741
|
T | A | 23 | a0001c0004t0001g0009a0001c0004t0001g0326a0001c0005t0005g0319others(20): Show | 23 | HG00544.hp1 HG01346.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.1275+90A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817741 | ||||||
| chr12:7817743
|
T | G | 193 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1275+88A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817743 | ||||||
| chr12:7817745
|
T | A | 15 | a0001c0005t0005g0327a0001c0006t0004g0038a0001c0006t0004g0046others(12): Show | 15 | HG00609.hp2 HG02040.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1275+86A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817745 | ||||||
| chr12:7817747
|
T | G | 216 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1275+84A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817747 | ||||||
| chr12:7817747
|
T | TATAGATA others(5): Show |
1 | a0001c0004t0001g0333 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1275+83_1275+84ins others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817747 | ||||||
| chr12:7817747
|
T | TATAGATA others(9): Show |
4 | a0001c0004t0001g0096a0001c0004t0001g0097a0001c0004t0001g0106others(1): Show | 4 | HG00639.hp1 HG01257.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1275+83_1275+84ins others(16): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817747 | ||||||
| chr12:7817747
|
T | TATAGATA others(13): Show |
1 | a0001c0004t0001g0123 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1275+83_1275+84ins others(20): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817747 | ||||||
| chr12:7817751
|
T | G | 237 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1275+80A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817751 | ||||||
| chr12:7817751
|
T | TATAGATA others(5): Show |
1 | a0001c0004t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1275+68_1275+79dup others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817751 | ||||||
| chr12:7817751
|
T | TATAGATA others(9): Show |
11 | a0001c0004t0001g0171a0001c0004t0001g0195a0001c0004t0001g0198others(8): Show | 11 | HG00639.hp2 HG01123.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1275+64_1275+79dup others(16): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817751 | ||||||
| chr12:7817751
|
T | TATAGATA others(13): Show |
17 | a0001c0004t0001g0011a0001c0004t0001g0069a0001c0004t0001g0071others(14): Show | 17 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1275+60_1275+79dup others(20): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817751 | ||||||
| chr12:7817751
|
T | TATATATA others(13): Show |
1 | a0001c0004t0001g0197 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1275+79_1275+80ins others(20): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817751 | ||||||
| chr12:7817781
|
C | T | 38 | a0001c0004t0001g0009a0001c0004t0001g0326a0001c0005t0005g0319others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.1275+50G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817781 | ||||||
| chr12:7817787
|
C | G | 38 | a0001c0004t0001g0009a0001c0004t0001g0326a0001c0005t0005g0319others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.1275+44G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817787 | ||||||
| chr12:7817793
|
T | C | 38 | a0001c0004t0001g0009a0001c0004t0001g0326a0001c0005t0005g0319others(35): Show | 38 | HG00544.hp1 HG00609.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.1275+38A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817793 | ||||||
| chr12:7817795
|
G | C | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275+36C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 10/10 | chr12 | 7817795 | ||||||
| chr12:7818125
|
T | G | 123 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0011others(120): Show | 124 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1072-91A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7818125 | ||||||
| chr12:7818129
|
C | T | 2 | a0001c0004t0001g0009a0001c0007t0018g0346 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1072-95G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7818129 | ||||||
| chr12:7818206
|
C | T | 1 | a0002c0010t0002g0243 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1072-172G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7818206 | ||||||
| chr12:7818218
|
C | CTG | 116 | a0001c0004t0001g0011a0001c0004t0001g0069a0001c0004t0001g0071others(113): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1072-186_1072-185d others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7818218 | ||||||
| chr12:7818401
|
C | T | 1 | a0001c0002t0003g0085 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1072-367G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7818401 | ||||||
| chr12:7818605
|
T | C | 15 | a0001c0008t0001g0004a0001c0008t0001g0023a0001c0008t0001g0025others(12): Show | 15 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.1072-571A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7818605 | ||||||
| chr12:7818618
|
C | T | 187 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(184): Show | 188 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1072-584G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7818618 | ||||||
| chr12:7818657
|
G | A | 187 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(184): Show | 188 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1072-623C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7818657 | ||||||
| chr12:7818691
|
C | CTT | 191 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(188): Show | 192 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1072-659_1072-658d others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7818691 | ||||||
| chr12:7818761
|
A | G | 1 | a0003c0014t0011g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1071+721T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7818761 | ||||||
| chr12:7818970
|
C | A | 1 | a0001c0007t0004g0230 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1071+512G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7818970 | ||||||
| chr12:7818984
|
G | C | 1 | a0001c0007t0004g0230 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1071+498C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7818984 | ||||||
| chr12:7819016
|
G | A | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1071+466C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7819016 | ||||||
| chr12:7819034
|
A | T | 114 | a0001c0004t0001g0011a0001c0004t0001g0069a0001c0004t0001g0071others(111): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1071+448T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7819034 | ||||||
| chr12:7819109
|
C | T | 2 | a0001c0003t0001g0314a0002c0013t0002g0182 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1071+373G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7819109 | ||||||
| chr12:7819114
|
G | A | 2 | a0001c0002t0003g0108a0001c0002t0003g0128 | 2 | HG01261.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1071+368C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7819114 | ||||||
| chr12:7819120
|
T | C | 5 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0193others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1071+362A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7819120 | ||||||
| chr12:7819140
|
CCAGGAGG others(16): Show |
C | 3 | a0001c0002t0003g0257a0001c0002t0003g0258a0001c0002t0003g0337 | 3 | HG00642.hp1 HG01255.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1071+319_1071+341d others(25): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7819140 | ||||||
| chr12:7819164
|
C | T | 3 | a0001c0002t0003g0257a0001c0002t0003g0258a0001c0002t0003g0337 | 3 | HG00642.hp1 HG01255.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1071+318G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7819164 | ||||||
| chr12:7819213
|
G | A | 34 | a0001c0004t0001g0011a0001c0004t0001g0069a0001c0004t0001g0071others(31): Show | 34 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1071+269C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7819213 | ||||||
| chr12:7819237
|
C | A | 187 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(184): Show | 188 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1071+245G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7819237 | ||||||
| chr12:7819321
|
C | T | 1 | a0001c0004t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1071+161G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7819321 | ||||||
| chr12:7819327
|
T | C | 5 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+155A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7819327 | ||||||
| chr12:7819478
|
T | C | 15 | a0001c0008t0001g0004a0001c0008t0001g0023a0001c0008t0001g0025others(12): Show | 15 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.1071+4A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 9/10 | chr12 | 7819478 | ||||||
| chr12:7819626
|
T | C | 2 | a0001c0006t0004g0038a0001c0006t0004g0164 | 2 | NA18980.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.970-43A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7819626 | ||||||
| chr12:7819697
|
G | A | 30 | a0001c0004t0001g0069a0001c0004t0001g0071a0001c0004t0001g0096others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.970-114C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7819697 | ||||||
| chr12:7819874
|
C | T | 16 | a0001c0003t0001g0313a0001c0008t0001g0004a0001c0008t0001g0023others(13): Show | 16 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.970-291G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7819874 | ||||||
| chr12:7820018
|
T | A | 194 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(191): Show | 195 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.970-435A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820018 | ||||||
| chr12:7820090
|
T | C | 342 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(339): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.970-507A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820090 | ||||||
| chr12:7820231
|
T | C | 201 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(198): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.970-648A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820231 | ||||||
| chr12:7820471
|
C | A | 347 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.969+750G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820471 | ||||||
| chr12:7820480
|
T | A | 26 | a0001c0004t0001g0009a0001c0006t0004g0035a0001c0006t0004g0038others(23): Show | 26 | HG00544.hp1 HG00609.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.969+741A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820480 | ||||||
| chr12:7820528
|
C | A | 1 | a0001c0003t0001g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.969+693G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820528 | ||||||
| chr12:7820534
|
C | T | 1 | a0003c0014t0011g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.969+687G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820534 | ||||||
| chr12:7820556
|
G | A | 1 | a0001c0003t0001g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.969+665C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820556 | ||||||
| chr12:7820637
|
C | T | 15 | a0001c0008t0001g0004a0001c0008t0001g0023a0001c0008t0001g0025others(12): Show | 15 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.969+584G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820637 | ||||||
| chr12:7820728
|
T | TC | 201 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(198): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.969+492dupG | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820728 | ||||||
| chr12:7820737
|
G | T | 3 | a0002c0001t0002g0321a0002c0001t0002g0322a0002c0001t0002g0325 | 3 | HG01928.hp2 HG01943.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.969+484C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820737 | ||||||
| chr12:7820859
|
G | T | 9 | a0001c0004t0001g0127a0001c0004t0001g0268a0001c0007t0007g0209others(6): Show | 9 | HG02486.hp1 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.969+362C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820859 | ||||||
| chr12:7820956
|
G | A | 194 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(191): Show | 195 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.969+265C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820956 | ||||||
| chr12:7820979
|
C | T | 16 | a0001c0008t0001g0004a0001c0008t0001g0023a0001c0008t0001g0025others(13): Show | 16 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.969+242G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 8/10 | chr12 | 7820979 | ||||||
| chr12:7821621
|
A | T | 1 | a0001c0002t0003g0041 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.865-296T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7821621 | ||||||
| chr12:7821655
|
C | T | 1 | a0001c0004t0001g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.865-330G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7821655 | ||||||
| chr12:7821751
|
G | A | 1 | a0001c0004t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.865-426C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7821751 | ||||||
| chr12:7821768
|
G | A | 86 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(83): Show | 86 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.865-443C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7821768 | ||||||
| chr12:7821797
|
C | T | 10 | a0001c0004t0001g0007a0001c0004t0001g0127a0001c0004t0001g0268others(7): Show | 10 | HG02486.hp1 HG02886.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.865-472G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7821797 | ||||||
| chr12:7821825
|
C | CT | 29 | a0001c0002t0003g0054a0001c0003t0001g0226a0001c0004t0001g0009others(26): Show | 29 | HG00673.hp1 HG01346.hp2 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.865-501dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7821825 | ||||||
| chr12:7821825
|
C | CTT | 201 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(198): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.865-502_865-501dup others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7821825 | ||||||
| chr12:7821887
|
C | T | 6 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0114others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.865-562G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7821887 | ||||||
| chr12:7821948
|
C | G | 2 | a0001c0003t0001g0314a0002c0013t0002g0182 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.865-623G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7821948 | ||||||
| chr12:7822006
|
A | G | 2 | a0001c0005t0005g0061a0001c0005t0005g0062 | 2 | HG02080.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.865-681T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822006 | ||||||
| chr12:7822135
|
T | C | 1 | a0001c0006t0009g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.865-810A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822135 | ||||||
| chr12:7822140
|
T | C | 4 | a0001c0003t0001g0024a0001c0003t0001g0047a0001c0003t0001g0083others(1): Show | 4 | HG02027.hp1 HG02155.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.865-815A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822140 | ||||||
| chr12:7822197
|
G | A | 2 | a0001c0002t0003g0044a0001c0002t0003g0196 | 2 | HG00423.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.865-872C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822197 | ||||||
| chr12:7822223
|
C | T | 14 | a0001c0008t0001g0004a0001c0008t0001g0023a0001c0008t0001g0025others(11): Show | 14 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.865-898G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822223 | ||||||
| chr12:7822239
|
G | A | 100 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.865-914C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822239 | ||||||
| chr12:7822443
|
A | T | 86 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(83): Show | 86 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.865-1118T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822443 | ||||||
| chr12:7822449
|
C | T | 2 | a0001c0002t0003g0142a0001c0002t0003g0260 | 2 | HG01074.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.865-1124G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822449 | ||||||
| chr12:7822618
|
G | A | 81 | a0001c0004t0001g0339a0001c0016t0008g0152a0002c0001t0002g0001others(78): Show | 82 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.865-1293C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822618 | ||||||
| chr12:7822650
|
C | T | 18 | a0001c0005t0005g0120a0001c0005t0005g0213a0001c0005t0005g0229others(15): Show | 18 | HG00408.hp1 HG00673.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.865-1325G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822650 | ||||||
| chr12:7822668
|
C | CA | 189 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.865-1344dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822668 | ||||||
| chr12:7822668
|
C | CAA | 12 | a0001c0002t0003g0107a0001c0002t0003g0126a0001c0003t0001g0047others(9): Show | 12 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.865-1345_865-1344d others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822668 | ||||||
| chr12:7822893
|
G | A | 1 | a0001c0007t0004g0019 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.865-1568C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822893 | ||||||
| chr12:7822911
|
T | A | 2 | a0001c0002t0003g0082a0001c0002t0003g0141 | 2 | HG02602.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.865-1586A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822911 | ||||||
| chr12:7822963
|
T | C | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.865-1638A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822963 | ||||||
| chr12:7822994
|
T | A | 8 | a0001c0003t0001g0018a0001c0003t0001g0056a0001c0003t0001g0058others(5): Show | 8 | NA18941.hp1 NA18945.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.865-1669A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822994 | ||||||
| chr12:7822999
|
T | C | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.865-1674A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7822999 | ||||||
| chr12:7823004
|
T | C | 1 | a0002c0001t0002g0305 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.865-1679A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823004 | ||||||
| chr12:7823078
|
C | A | 3 | a0001c0003t0010g0013a0001c0003t0010g0014a0001c0003t0010g0098 | 3 | HG01952.hp1 HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.865-1753G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823078 | ||||||
| chr12:7823098
|
G | A | 3 | a0001c0004t0001g0326a0001c0005t0005g0319a0001c0005t0005g0327 | 3 | HG02572.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.865-1773C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823098 | ||||||
| chr12:7823153
|
C | A | 204 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(201): Show | 205 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.865-1828G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823153 | ||||||
| chr12:7823254
|
G | A | 204 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(201): Show | 205 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.865-1929C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823254 | ||||||
| chr12:7823382
|
C | CA | 202 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(199): Show | 203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.865-2058dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823382 | ||||||
| chr12:7823426
|
C | T | 211 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(208): Show | 212 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.865-2101G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823426 | ||||||
| chr12:7823448
|
C | T | 204 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(201): Show | 205 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.865-2123G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823448 | ||||||
| chr12:7823460
|
C | T | 1 | a0003c0012t0011g0113 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.865-2135G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823460 | ||||||
| chr12:7823474
|
G | C | 105 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.865-2149C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823474 | ||||||
| chr12:7823528
|
C | T | 14 | a0001c0003t0001g0117a0001c0003t0001g0135a0001c0003t0001g0136others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.865-2203G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823528 | ||||||
| chr12:7823589
|
G | A | 203 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(200): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.865-2264C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823589 | ||||||
| chr12:7823645
|
G | A | 1 | a0001c0002t0003g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.865-2320C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823645 | ||||||
| chr12:7823651
|
T | C | 1 | a0001c0003t0001g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.865-2326A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823651 | ||||||
| chr12:7823720
|
C | CA | 214 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(211): Show | 215 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.865-2396dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823720 | ||||||
| chr12:7823945
|
C | T | 343 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.865-2620G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823945 | ||||||
| chr12:7823995
|
A | T | 1 | a0003c0014t0011g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.865-2670T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7823995 | ||||||
| chr12:7824239
|
G | A | 14 | a0001c0008t0001g0004a0001c0008t0001g0023a0001c0008t0001g0025others(11): Show | 14 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.865-2914C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824239 | ||||||
| chr12:7824271
|
A | T | 203 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(200): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.865-2946T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824271 | ||||||
| chr12:7824330
|
C | G | 33 | a0001c0005t0005g0033a0001c0005t0005g0039a0001c0005t0005g0061others(30): Show | 33 | HG00408.hp1 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.865-3005G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824330 | ||||||
| chr12:7824432
|
C | T | 1 | a0001c0004t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.864+3063G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824432 | ||||||
| chr12:7824465
|
G | A | 1 | a0002c0001t0002g0177 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.864+3030C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824465 | ||||||
| chr12:7824498
|
C | T | 203 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(200): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.864+2997G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824498 | ||||||
| chr12:7824663
|
G | A | 1 | a0003c0014t0011g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.864+2832C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824663 | ||||||
| chr12:7824668
|
A | G | 203 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(200): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.864+2827T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824668 | ||||||
| chr12:7824672
|
G | A | 14 | a0001c0008t0001g0004a0001c0008t0001g0023a0001c0008t0001g0025others(11): Show | 14 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.864+2823C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824672 | ||||||
| chr12:7824697
|
C | T | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+2798G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824697 | ||||||
| chr12:7824707
|
G | A | 14 | a0001c0008t0001g0004a0001c0008t0001g0023a0001c0008t0001g0025others(11): Show | 14 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.864+2788C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824707 | ||||||
| chr12:7824728
|
C | CA | 209 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.864+2766dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824728 | ||||||
| chr12:7824728
|
C | CAA | 80 | a0001c0002t0003g0087a0001c0002t0003g0126a0001c0003t0001g0018others(77): Show | 80 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.864+2765_864+2766d others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824728 | ||||||
| chr12:7824755
|
T | C | 203 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(200): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.864+2740A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824755 | ||||||
| chr12:7824852
|
G | A | 2 | a0002c0009t0002g0026a0002c0009t0002g0264 | 2 | HG02155.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.864+2643C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824852 | ||||||
| chr12:7824897
|
G | T | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+2598C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824897 | ||||||
| chr12:7824913
|
T | C | 1 | a0001c0003t0001g0219 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.864+2582A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824913 | ||||||
| chr12:7824938
|
G | GC | 8 | a0001c0006t0004g0115a0001c0006t0004g0157a0001c0006t0004g0158others(5): Show | 8 | HG02145.hp2 HG02895.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.864+2556dupG | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824938 | ||||||
| chr12:7824956
|
C | A | 331 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.864+2539G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824956 | ||||||
| chr12:7824986
|
T | C | 344 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(341): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.864+2509A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7824986 | ||||||
| chr12:7825127
|
T | C | 203 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(200): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.864+2368A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825127 | ||||||
| chr12:7825177
|
T | C | 203 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(200): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.864+2318A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825177 | ||||||
| chr12:7825182
|
T | C | 2 | a0002c0001t0002g0179a0002c0001t0002g0245 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.864+2313A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825182 | ||||||
| chr12:7825183
|
G | A | 2 | a0002c0001t0002g0179a0002c0001t0002g0245 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.864+2312C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825183 | ||||||
| chr12:7825188
|
T | C | 2 | a0002c0001t0002g0179a0002c0001t0002g0245 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.864+2307A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825188 | ||||||
| chr12:7825235
|
T | TG | 106 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.864+2259dupC | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825235 | ||||||
| chr12:7825249
|
CCAGGAGT others(294): Show |
C | 4 | a0001c0002t0003g0257a0001c0002t0003g0258a0001c0002t0003g0302others(1): Show | 4 | HG00642.hp1 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+1945_864+2245d others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825249 | ||||||
| chr12:7825288
|
C | T | 203 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(200): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.864+2207G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825288 | ||||||
| chr12:7825318
|
T | C | 203 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(200): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.864+2177A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825318 | ||||||
| chr12:7825364
|
G | A | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+2131C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825364 | ||||||
| chr12:7825459
|
C | CA | 99 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.864+2035dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825459 | ||||||
| chr12:7825459
|
CA | C | 203 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(200): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.864+2035delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825459 | ||||||
| chr12:7825489
|
C | A | 103 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.864+2006G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825489 | ||||||
| chr12:7825578
|
A | G | 4 | a0001c0004t0001g0127a0001c0004t0001g0268a0001c0007t0009g0078others(1): Show | 4 | HG02886.hp1 HG03098.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+1917T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825578 | ||||||
| chr12:7825590
|
A | G | 76 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(73): Show | 76 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.864+1905T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825590 | ||||||
| chr12:7825711
|
A | G | 197 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(194): Show | 198 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.864+1784T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825711 | ||||||
| chr12:7825766
|
C | CAAA | 10 | a0001c0003t0001g0186a0001c0003t0001g0192a0001c0003t0001g0316others(7): Show | 10 | HG01123.hp1 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.864+1726_864+1728d others(5): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825766 | ||||||
| chr12:7825766
|
C | CAAAA | 159 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(156): Show | 160 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.864+1725_864+1728d others(6): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825766 | ||||||
| chr12:7825766
|
C | CAAAAA | 28 | a0001c0003t0001g0047a0001c0003t0001g0056a0001c0003t0001g0067others(25): Show | 28 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.864+1724_864+1728d others(7): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825766 | ||||||
| chr12:7825766
|
CA | C | 6 | a0001c0004t0001g0016a0001c0004t0001g0326a0001c0005t0005g0319others(3): Show | 6 | HG01109.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.864+1728delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825766 | ||||||
| chr12:7825766
|
CAA | C | 128 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.864+1727_864+1728d others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825766 | ||||||
| chr12:7825766
|
CAAA | C | 15 | a0001c0008t0001g0004a0001c0008t0001g0023a0001c0008t0001g0025others(12): Show | 15 | HG00673.hp1 HG01884.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.864+1726_864+1728d others(5): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825766 | ||||||
| chr12:7825787
|
A | G | 1 | a0001c0002t0003g0079 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.864+1708T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825787 | ||||||
| chr12:7825796
|
G | GA | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1698dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825796 | ||||||
| chr12:7825819
|
C | CCA | 331 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.864+1674_864+1675d others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825819 | ||||||
| chr12:7825961
|
T | C | 14 | a0001c0008t0001g0004a0001c0008t0001g0023a0001c0008t0001g0025others(11): Show | 14 | HG00673.hp1 HG02083.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.864+1534A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825961 | ||||||
| chr12:7825969
|
C | CT | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1525dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825969 | ||||||
| chr12:7825980
|
T | A | 3 | a0002c0001t0002g0012a0002c0001t0002g0270a0002c0001t0002g0271 | 3 | HG01884.hp2 HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.864+1515A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7825980 | ||||||
| chr12:7826000
|
G | A | 76 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(73): Show | 76 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.864+1495C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826000 | ||||||
| chr12:7826107
|
A | G | 24 | a0001c0003t0001g0117a0001c0003t0001g0135a0001c0003t0001g0136others(21): Show | 24 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.864+1388T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826107 | ||||||
| chr12:7826134
|
A | G | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1361T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826134 | ||||||
| chr12:7826146
|
C | T | 80 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(77): Show | 80 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.864+1349G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826146 | ||||||
| chr12:7826225
|
G | GT | 216 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(213): Show | 217 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.864+1269dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826225 | ||||||
| chr12:7826225
|
G | GTT | 119 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.864+1268_864+1269d others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826225 | ||||||
| chr12:7826225
|
G | GTTT | 10 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0114others(7): Show | 10 | HG01884.hp1 HG02074.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.864+1267_864+1269d others(5): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826225 | ||||||
| chr12:7826242
|
G | A | 1 | a0001c0002t0003g0122 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.864+1253C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826242 | ||||||
| chr12:7826554
|
G | C | 1 | a0001c0002t0003g0089 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.864+941C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826554 | ||||||
| chr12:7826807
|
G | C | 2 | a0001c0005t0005g0342a0005c0015t0008g0341 | 2 | HG02280.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.864+688C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826807 | ||||||
| chr12:7826830
|
T | C | 2 | a0001c0004t0001g0285a0001c0004t0001g0344 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.864+665A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826830 | ||||||
| chr12:7826834
|
T | C | 7 | a0001c0003t0001g0298a0001c0003t0001g0313a0001c0004t0001g0007others(4): Show | 7 | HG01884.hp1 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.864+661A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826834 | ||||||
| chr12:7826834
|
T | TTTCCTTC others(5): Show |
1 | a0001c0002t0003g0142 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.864+649_864+660dup others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826834 | ||||||
| chr12:7826834
|
T | TTTCCTTC others(29): Show |
1 | a0001c0006t0016g0273 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.864+660_864+661ins others(36): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826834 | ||||||
| chr12:7826834
|
T | TTTCCTTC others(33): Show |
2 | a0001c0003t0001g0028a0001c0008t0001g0045 | 2 | NA18969.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.864+660_864+661ins others(40): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826834 | ||||||
| chr12:7826834
|
T | TTTCCTTC others(37): Show |
1 | a0002c0013t0002g0182 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.864+660_864+661ins others(44): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826834 | ||||||
| chr12:7826834
|
T | TTTCCTTC others(41): Show |
2 | a0001c0003t0001g0058a0001c0003t0001g0116 | 2 | HG02129.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.864+660_864+661ins others(48): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826834 | ||||||
| chr12:7826834
|
T | TTTCCTTC others(45): Show |
1 | a0001c0008t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.864+660_864+661ins others(52): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826834 | ||||||
| chr12:7826839
|
T | C | 2 | a0001c0005t0005g0193a0001c0005t0005g0340 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.864+656A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826839 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(65): Show |
1 | a0001c0003t0001g0018 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(72): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(72): Show |
1 | a0001c0008t0001g0274 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.864+641_864+642ins others(79): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(57): Show |
1 | a0001c0003t0001g0083 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(64): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(53): Show |
5 | a0001c0003t0001g0135a0001c0003t0001g0136a0001c0003t0001g0190others(2): Show | 5 | HG02040.hp2 HG02145.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.864+641_864+642ins others(60): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(57): Show |
1 | a0001c0008t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.864+641_864+642ins others(64): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(65): Show |
1 | a0001c0003t0001g0117 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(72): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(49): Show |
3 | a0001c0003t0001g0068a0001c0003t0001g0191a0001c0006t0004g0137 | 3 | HG01496.hp2 HG02055.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.864+641_864+642ins others(56): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(58): Show |
1 | a0001c0003t0001g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(65): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(45): Show |
4 | a0001c0003t0001g0024a0001c0003t0001g0056a0001c0006t0004g0073others(1): Show | 4 | HG01943.hp1 HG01993.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+641_864+642ins others(52): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(60): Show |
1 | a0001c0003t0001g0320 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(67): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(64): Show |
1 | a0001c0006t0004g0046 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(71): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(41): Show |
6 | a0001c0003t0001g0060a0001c0003t0012g0057a0001c0006t0004g0051others(3): Show | 6 | HG00609.hp2 NA18948.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.864+641_864+642ins others(48): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(52): Show |
1 | a0001c0008t0001g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(59): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(56): Show |
1 | a0001c0003t0001g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.864+641_864+642ins others(63): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(37): Show |
5 | a0001c0003t0001g0095a0001c0003t0001g0130a0001c0003t0001g0225others(2): Show | 5 | HG00609.hp1 HG02080.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+641_864+642ins others(44): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(45): Show |
1 | a0001c0003t0001g0221 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.864+641_864+642ins others(52): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(48): Show |
2 | a0001c0003t0001g0244a0001c0003t0001g0328 | 2 | HG01891.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.864+641_864+642ins others(55): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(52): Show |
1 | a0001c0003t0001g0219 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(59): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(33): Show |
3 | a0001c0003t0001g0145a0001c0003t0001g0218a0001c0003t0001g0317 | 3 | NA19064.hp1 NA19070.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.864+641_864+642ins others(40): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(44): Show |
1 | a0001c0003t0001g0226 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.864+641_864+642ins others(51): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(29): Show |
2 | a0001c0003t0001g0042a0001c0006t0009g0081 | 2 | HG02083.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.864+641_864+642ins others(36): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(40): Show |
1 | a0001c0006t0004g0212 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(47): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(44): Show |
1 | a0001c0006t0004g0233 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.864+641_864+642ins others(51): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(25): Show |
2 | a0001c0003t0001g0318a0002c0001t0002g0149 | 2 | HG00438.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.864+641_864+642ins others(32): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(33): Show |
1 | a0001c0003t0001g0290 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.864+641_864+642ins others(40): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(36): Show |
2 | a0001c0003t0001g0188a0001c0003t0001g0330 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.864+641_864+642ins others(43): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(52): Show |
1 | a0001c0003t0001g0189 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.864+641_864+642ins others(59): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(21): Show |
1 | a0001c0003t0001g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.864+641_864+642ins others(28): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(17): Show |
1 | a0002c0001t0002g0231 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(24): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(9): Show |
13 | a0001c0005t0005g0229a0001c0016t0008g0152a0002c0001t0002g0001others(10): Show | 14 | HG00140.hp1 HG00323.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.864+641_864+642ins others(16): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(17): Show |
1 | a0002c0001t0002g0131 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(24): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(20): Show |
1 | a0004c0017t0002g0129 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(27): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(28): Show |
1 | a0002c0001t0002g0174 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(35): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(18): Show |
1 | a0001c0002t0003g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.864+641_864+642ins others(25): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(5): Show |
39 | a0001c0002t0003g0066a0001c0002t0003g0082a0001c0002t0003g0092others(36): Show | 39 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.864+641_864+642ins others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(20): Show |
4 | a0002c0001t0002g0276a0002c0009t0002g0264a0002c0010t0002g0049others(1): Show | 4 | HG02523.hp2 HG03942.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+641_864+642ins others(27): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(24): Show |
2 | a0002c0001t0002g0151a0002c0009t0002g0026 | 2 | HG02015.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.864+641_864+642ins others(31): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(18): Show |
2 | a0001c0002t0003g0044a0001c0002t0003g0293 | 2 | HG00423.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.864+641_864+642ins others(25): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(22): Show |
1 | a0001c0002t0003g0089 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.864+641_864+642ins others(29): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(12): Show |
2 | a0001c0004t0001g0009a0001c0007t0018g0346 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.864+641_864+642ins others(19): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | CCTTCCTT others(1): Show |
3 | a0002c0001t0002g0036a0002c0001t0002g0301a0002c0011t0008g0289 | 3 | HG04115.hp1 HG04199.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.864+641_864+642ins others(8): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826853
|
C | T | 3 | a0001c0005t0005g0319a0001c0007t0009g0078a0001c0007t0009g0291 | 3 | HG02886.hp1 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.864+642G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826853 | ||||||
| chr12:7826854
|
C | CTTCCTTC others(56): Show |
1 | a0001c0006t0004g0038 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.864+640_864+641ins others(63): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826854 | ||||||
| chr12:7826854
|
C | CTTCCTTC others(60): Show |
1 | a0001c0003t0001g0298 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.864+640_864+641ins others(67): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826854 | ||||||
| chr12:7826854
|
C | CTTCCTTC others(56): Show |
3 | a0001c0006t0004g0246a0001c0008t0001g0023a0001c0008t0001g0025 | 3 | HG02135.hp1 NA18947.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.864+640_864+641ins others(63): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826854 | ||||||
| chr12:7826854
|
C | CTTCCTTC others(48): Show |
1 | a0001c0006t0004g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.864+640_864+641ins others(55): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826854 | ||||||
| chr12:7826854
|
C | CTTCCTTC others(44): Show |
5 | a0001c0003t0001g0047a0001c0003t0001g0186a0001c0003t0001g0222others(2): Show | 5 | HG00544.hp1 HG02572.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.864+640_864+641ins others(51): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826854 | ||||||
| chr12:7826854
|
C | CTTCCTTC others(36): Show |
2 | a0001c0003t0001g0192a0001c0003t0001g0316 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.864+640_864+641ins others(43): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826854 | ||||||
| chr12:7826854
|
C | CTTCCTTC others(32): Show |
2 | a0001c0003t0001g0187a0001c0003t0001g0272 | 2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.864+640_864+641ins others(39): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826854 | ||||||
| chr12:7826854
|
C | CTTCCTTC others(19): Show |
1 | a0001c0002t0003g0093 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.864+640_864+641ins others(26): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826854 | ||||||
| chr12:7826854
|
C | CTTCCTTC others(18): Show |
1 | a0001c0002t0003g0085 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.864+640_864+641ins others(25): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826854 | ||||||
| chr12:7826854
|
C | CTTCCTTC others(14): Show |
1 | a0001c0002t0003g0260 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.864+640_864+641ins others(21): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826854 | ||||||
| chr12:7826854
|
C | CTTCCTTC others(8): Show |
1 | a0001c0007t0004g0146 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.864+640_864+641ins others(15): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826854 | ||||||
| chr12:7826854
|
C | CTTCCTTC others(14): Show |
7 | a0001c0002t0003g0020a0001c0002t0003g0053a0001c0002t0003g0055others(4): Show | 7 | HG01106.hp2 HG02004.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+640_864+641ins others(21): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826854 | ||||||
| chr12:7826855
|
T | TTCCTTCC others(48): Show |
1 | a0001c0006t0004g0164 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.864+639_864+640ins others(55): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826855 | ||||||
| chr12:7826856
|
T | TCCTTCCT others(11): Show |
2 | a0001c0002t0003g0054a0001c0005t0005g0213 | 2 | NA18949.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.864+638_864+639ins others(18): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826856 | ||||||
| chr12:7826856
|
T | TCCTTCCT others(7): Show |
11 | a0001c0002t0003g0031a0001c0002t0003g0094a0001c0002t0003g0108others(8): Show | 11 | HG00738.hp2 HG01261.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.864+638_864+639ins others(14): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826856 | ||||||
| chr12:7826857
|
T | C | 158 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0041others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.864+638A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826857 | ||||||
| chr12:7826858
|
C | CTTCCTTC others(50): Show |
1 | a0001c0003t0001g0067 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.864+636_864+637ins others(57): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826858 | ||||||
| chr12:7826858
|
C | CTTCCTTC others(42): Show |
1 | a0001c0003t0001g0153 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.864+636_864+637ins others(49): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826858 | ||||||
| chr12:7826858
|
C | T | 16 | a0001c0002t0003g0031a0001c0002t0003g0054a0001c0002t0003g0093others(13): Show | 16 | HG00738.hp2 HG01175.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.864+637G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826858 | ||||||
| chr12:7826858
|
CTTT | C | 4 | a0001c0005t0005g0205a0001c0005t0005g0335a0001c0005t0005g0336others(1): Show | 4 | HG01123.hp2 HG01496.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+634_864+636del others(3): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826858 | ||||||
| chr12:7826859
|
T | TTCCTTTC others(4): Show |
1 | a0001c0005t0006g0178 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.864+635_864+636ins others(11): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826859 | ||||||
| chr12:7826860
|
T | TC | 49 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0076others(46): Show | 49 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.864+634_864+635ins others(1): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTC | 15 | a0001c0004t0001g0171a0001c0004t0001g0197a0001c0004t0001g0294others(12): Show | 15 | HG00323.hp1 HG01099.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.864+634_864+635ins others(5): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTCCT others(2): Show |
8 | a0001c0004t0001g0010a0001c0004t0001g0015a0001c0004t0001g0106others(5): Show | 8 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.864+634_864+635ins others(9): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTCCT others(6): Show |
7 | a0001c0003t0010g0098a0001c0004t0001g0109a0001c0004t0001g0195others(4): Show | 7 | HG00280.hp2 HG00738.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.864+634_864+635ins others(13): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTCCT others(10): Show |
6 | a0001c0004t0001g0069a0001c0004t0001g0110a0001c0004t0001g0236others(3): Show | 6 | HG02257.hp1 HG02602.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.864+634_864+635ins others(17): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTCCT others(14): Show |
5 | a0001c0004t0001g0016a0001c0004t0001g0071a0001c0004t0001g0118others(2): Show | 5 | HG00735.hp2 HG01109.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.864+634_864+635ins others(21): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTCCT others(18): Show |
6 | a0001c0003t0001g0314a0001c0004t0001g0007a0001c0004t0001g0123others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.864+634_864+635ins others(25): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTCCT others(22): Show |
3 | a0001c0003t0010g0013a0001c0003t0014g0139a0001c0006t0004g0157 | 3 | HG02145.hp2 HG02155.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.864+634_864+635ins others(29): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTCCT others(26): Show |
6 | a0001c0004t0001g0254a0001c0005t0005g0255a0001c0006t0004g0158others(3): Show | 6 | HG02083.hp2 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+634_864+635ins others(33): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTCCT others(30): Show |
6 | a0001c0003t0010g0014a0001c0005t0005g0114a0001c0006t0004g0115others(3): Show | 6 | HG02258.hp2 HG02895.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+634_864+635ins others(37): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTCCT others(34): Show |
1 | a0001c0006t0004g0288 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.864+634_864+635ins others(41): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTCCT others(38): Show |
1 | a0001c0006t0004g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.864+634_864+635ins others(45): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTCCT others(46): Show |
1 | a0001c0008t0001g0004 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.864+634_864+635ins others(53): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTCCT others(7): Show |
1 | a0001c0002t0003g0041 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.864+634_864+635ins others(14): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826860
|
T | TCCTTTCT others(3): Show |
9 | a0001c0002t0003g0079a0001c0002t0003g0080a0001c0002t0003g0091others(6): Show | 9 | HG00099.hp1 HG00099.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.864+634_864+635ins others(10): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826860 | ||||||
| chr12:7826861
|
T | C | 126 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0076others(123): Show | 126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.864+634A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826861 | ||||||
| chr12:7826861
|
T | TC | 61 | a0001c0002t0003g0020a0001c0002t0003g0044a0001c0002t0003g0053others(58): Show | 61 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.864+633_864+634ins others(1): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826861 | ||||||
| chr12:7826861
|
T | TCTTTCTT others(7): Show |
1 | a0001c0002t0003g0280 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.864+633_864+634ins others(14): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826861 | ||||||
| chr12:7826861
|
T | TCTTTCTT others(11): Show |
2 | a0001c0002t0003g0100a0001c0002t0003g0283 | 2 | NA18975.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.864+633_864+634ins others(18): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826861 | ||||||
| chr12:7826861
|
T | TCTTTCTT others(15): Show |
1 | a0001c0002t0003g0148 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.864+633_864+634ins others(22): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826861 | ||||||
| chr12:7826861
|
T | TCTTTCTT others(16): Show |
1 | a0001c0002t0003g0087 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.864+633_864+634ins others(23): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826861 | ||||||
| chr12:7826861
|
T | TCTTTTTT others(5): Show |
8 | a0001c0007t0004g0027a0001c0007t0004g0203a0001c0007t0004g0230others(5): Show | 8 | HG00544.hp2 HG03688.hp1 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.864+633_864+634ins others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826861 | ||||||
| chr12:7826861
|
T | TCTTTTTT others(9): Show |
3 | a0001c0007t0004g0043a0002c0001t0002g0065a0002c0001t0002g0208 | 3 | HG02040.hp1 NA18959.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.864+633_864+634ins others(16): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826861 | ||||||
| chr12:7826861
|
T | TCTTTTTT others(13): Show |
2 | a0002c0001t0002g0155a0002c0001t0002g0310 | 2 | NA18944.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.864+633_864+634ins others(20): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826861 | ||||||
| chr12:7826861
|
T | TCTTTTTT others(17): Show |
1 | a0001c0007t0004g0019 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.864+633_864+634ins others(24): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826861 | ||||||
| chr12:7826861
|
T | TTTTTTC | 12 | a0001c0002t0003g0066a0001c0002t0003g0082a0001c0002t0003g0092others(9): Show | 12 | HG00642.hp2 HG01433.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.864+633_864+634ins others(6): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826861 | ||||||
| chr12:7826862
|
T | C | 16 | a0001c0003t0001g0116a0001c0004t0001g0011a0001c0004t0001g0017others(13): Show | 16 | HG00639.hp1 HG01257.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.864+633A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826862 | ||||||
| chr12:7826863
|
T | C | 1 | a0001c0002t0003g0075 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.864+632A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826863 | ||||||
| chr12:7826864
|
T | C | 59 | a0001c0003t0001g0314a0001c0003t0010g0013a0001c0003t0010g0014others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.864+631A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826864 | ||||||
| chr12:7826865
|
C | T | 17 | a0001c0002t0003g0041a0001c0002t0003g0075a0001c0002t0003g0079others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.864+630G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826865 | ||||||
| chr12:7826866
|
T | C | 11 | a0001c0004t0001g0011a0001c0004t0001g0017a0001c0004t0001g0096others(8): Show | 11 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.864+629A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826866 | ||||||
| chr12:7826868
|
T | C | 42 | a0001c0003t0014g0139a0001c0004t0001g0007a0001c0004t0001g0010others(39): Show | 42 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.864+627A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826868 | ||||||
| chr12:7826869
|
C | CT | 22 | a0001c0002t0003g0021a0001c0002t0003g0105a0001c0002t0003g0125others(19): Show | 22 | HG00280.hp1 HG00408.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.864+625dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826869 | ||||||
| chr12:7826869
|
C | CTTT | 7 | a0001c0008t0001g0004a0002c0001t0002g0088a0002c0001t0002g0163others(4): Show | 7 | HG00621.hp2 HG01934.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+623_864+625dup others(3): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826869 | ||||||
| chr12:7826869
|
C | CTTTTT | 14 | a0001c0002t0003g0022a0001c0002t0003g0076a0001c0002t0003g0090others(11): Show | 14 | HG00140.hp2 HG00673.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.864+625_864+626ins others(5): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826869 | ||||||
| chr12:7826869
|
C | T | 1 | a0001c0002t0003g0302 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.864+626G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826869 | ||||||
| chr12:7826870
|
T | C | 11 | a0001c0004t0001g0011a0001c0004t0001g0017a0001c0004t0001g0096others(8): Show | 11 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.864+625A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826870 | ||||||
| chr12:7826870
|
TTTC | T | 7 | a0001c0005t0005g0140a0001c0005t0005g0172a0001c0005t0005g0173others(4): Show | 7 | HG01074.hp1 HG01168.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.864+622_864+624del others(3): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826870 | ||||||
| chr12:7826872
|
T | C | 37 | a0001c0003t0014g0139a0001c0004t0001g0007a0001c0004t0001g0010others(34): Show | 37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.864+623A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826872 | ||||||
| chr12:7826872
|
TC | T | 13 | a0001c0004t0001g0339a0001c0006t0009g0284a0001c0008t0001g0238others(10): Show | 13 | HG01099.hp1 HG01167.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.864+622delG | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826872 | ||||||
| chr12:7826873
|
C | T | 22 | a0001c0002t0003g0021a0001c0002t0003g0105a0001c0002t0003g0125others(19): Show | 22 | HG00280.hp1 HG00408.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.864+622G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826873 | ||||||
| chr12:7826874
|
T | C | 11 | a0001c0004t0001g0011a0001c0004t0001g0017a0001c0004t0001g0096others(8): Show | 11 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.864+621A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826874 | ||||||
| chr12:7826874
|
TTTC | T | 4 | a0001c0005t0005g0205a0001c0005t0005g0335a0001c0005t0005g0336others(1): Show | 4 | HG01123.hp2 HG01496.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+618_864+620del others(3): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826874 | ||||||
| chr12:7826876
|
T | C | 31 | a0001c0003t0014g0139a0001c0004t0001g0007a0001c0004t0001g0010others(28): Show | 31 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.864+619A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826876 | ||||||
| chr12:7826876
|
TC | T | 14 | a0001c0003t0001g0314a0001c0003t0010g0013a0001c0003t0010g0014others(11): Show | 14 | HG01884.hp2 HG01952.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.864+618delG | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826876 | ||||||
| chr12:7826877
|
C | T | 7 | a0001c0005t0005g0140a0001c0005t0005g0172a0001c0005t0005g0173others(4): Show | 7 | HG01074.hp1 HG01168.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.864+618G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826877 | ||||||
| chr12:7826878
|
T | C | 11 | a0001c0004t0001g0011a0001c0004t0001g0017a0001c0004t0001g0096others(8): Show | 11 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.864+617A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826878 | ||||||
| chr12:7826880
|
T | C | 29 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(26): Show | 29 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.864+615A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826880 | ||||||
| chr12:7826881
|
C | T | 4 | a0001c0005t0005g0205a0001c0005t0005g0335a0001c0005t0005g0336others(1): Show | 4 | HG01123.hp2 HG01496.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+614G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826881 | ||||||
| chr12:7826882
|
T | C | 9 | a0001c0004t0001g0011a0001c0004t0001g0017a0001c0004t0001g0096others(6): Show | 9 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.864+613A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826882 | ||||||
| chr12:7826884
|
T | C | 1 | a0003c0014t0011g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.864+611A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826884 | ||||||
| chr12:7826884
|
TC | T | 6 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0114others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+610delG | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826884 | ||||||
| chr12:7826885
|
C | T | 1 | a0001c0005t0005g0224 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.864+610G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826885 | ||||||
| chr12:7826886
|
T | C | 9 | a0001c0004t0001g0011a0001c0004t0001g0017a0001c0004t0001g0096others(6): Show | 9 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.864+609A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826886 | ||||||
| chr12:7826888
|
T | C | 1 | a0003c0014t0011g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.864+607A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826888 | ||||||
| chr12:7826889
|
C | CCTTCCTT others(17): Show |
1 | a0001c0004t0001g0184 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.864+605_864+606ins others(24): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826889 | ||||||
| chr12:7826889
|
C | CCTTCCTT others(5): Show |
3 | a0001c0004t0001g0011a0001c0004t0001g0017a0001c0004t0001g0183 | 3 | HG02055.hp2 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.864+605_864+606ins others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826889 | ||||||
| chr12:7826889
|
C | CCTTT | 3 | a0001c0004t0001g0096a0001c0004t0001g0332a0001c0004t0001g0333 | 3 | HG00639.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.864+605_864+606ins others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826889 | ||||||
| chr12:7826889
|
C | T | 2 | a0001c0004t0001g0097a0001c0004t0001g0331 | 2 | HG01257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.864+606G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826889 | ||||||
| chr12:7826889
|
CT | C | 29 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(26): Show | 29 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.864+605delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826889 | ||||||
| chr12:7826890
|
T | C | 9 | a0001c0004t0001g0011a0001c0004t0001g0017a0001c0004t0001g0096others(6): Show | 9 | HG00639.hp1 HG01257.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.864+605A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826890 | ||||||
| chr12:7826892
|
T | C | 1 | a0003c0014t0011g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.864+603A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826892 | ||||||
| chr12:7826907
|
TTC | T | 27 | a0001c0003t0001g0018a0001c0003t0001g0042a0001c0003t0001g0056others(24): Show | 28 | HG00438.hp1 HG00597.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.864+586_864+587del others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826907 | ||||||
| chr12:7826909
|
C | CTT | 103 | a0001c0003t0001g0028a0001c0003t0001g0047a0001c0003t0001g0058others(100): Show | 103 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.864+584_864+585dup others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826909 | ||||||
| chr12:7826909
|
C | CTTTCTT | 21 | a0001c0003t0001g0024a0001c0003t0001g0130a0001c0003t0001g0190others(18): Show | 21 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.864+580_864+585dup others(6): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826909 | ||||||
| chr12:7826909
|
C | CTTTCTTT others(3): Show |
11 | a0002c0001t0002g0032a0002c0001t0002g0124a0002c0001t0002g0133others(8): Show | 11 | HG02074.hp2 HG02273.hp1 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.864+585_864+586ins others(10): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826909 | ||||||
| chr12:7826909
|
C | CTTTCTTT others(7): Show |
3 | a0002c0001t0002g0036a0002c0001t0002g0250a0002c0009t0002g0143 | 3 | HG00438.hp2 HG04199.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.864+585_864+586ins others(14): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826909 | ||||||
| chr12:7826925
|
TCTTTC | T | 34 | a0001c0004t0001g0011a0001c0004t0001g0069a0001c0004t0001g0071others(31): Show | 34 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.864+565_864+569del others(5): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826925 | ||||||
| chr12:7826955
|
TTC | T | 4 | a0001c0002t0003g0257a0001c0002t0003g0258a0001c0002t0003g0337others(1): Show | 4 | HG00642.hp1 HG01255.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+538_864+539del others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826955 | ||||||
| chr12:7826965
|
T | TTC | 40 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0011others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.864+528_864+529dup others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826965 | ||||||
| chr12:7826967
|
C | CTCTCTTT others(8): Show |
1 | a0001c0004t0001g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.864+527_864+528ins others(15): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826967 | ||||||
| chr12:7826969
|
CTCTCTCT others(10): Show |
C | 15 | a0001c0005t0005g0039a0001c0008t0001g0004a0001c0008t0001g0023others(12): Show | 15 | HG00673.hp1 HG02083.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.864+509_864+525del others(17): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826969 | ||||||
| chr12:7826984
|
C | T | 1 | a0002c0009t0002g0103 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.864+511G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826984 | ||||||
| chr12:7826986
|
T | C | 1 | a0002c0009t0002g0103 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.864+509A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826986 | ||||||
| chr12:7826986
|
T | TTC | 271 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(268): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.864+507_864+508dup others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826986 | ||||||
| chr12:7826986
|
T | TTCTCTCT others(14): Show |
3 | a0001c0004t0001g0127a0001c0007t0009g0078a0001c0007t0009g0291 | 3 | HG02886.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.864+508_864+509ins others(21): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826986 | ||||||
| chr12:7826986
|
T | TTCTCTCT others(18): Show |
3 | a0001c0004t0001g0326a0001c0005t0005g0319a0001c0005t0005g0327 | 3 | HG02572.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.864+508_864+509ins others(25): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826986 | ||||||
| chr12:7826986
|
TTC | T | 53 | a0001c0004t0001g0007a0001c0004t0001g0009a0001c0004t0001g0010others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.864+507_864+508del others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7826986 | ||||||
| chr12:7827026
|
TTCTC | T | 82 | a0001c0004t0001g0339a0001c0008t0001g0238a0001c0008t0001g0240others(79): Show | 83 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.864+465_864+468del others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827026 | ||||||
| chr12:7827042
|
C | CCTTTCTC others(11): Show |
2 | a0001c0003t0010g0013a0001c0003t0010g0014 | 2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.864+435_864+452dup others(18): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827042 | ||||||
| chr12:7827073
|
C | T | 3 | a0001c0003t0001g0318a0001c0004t0001g0285a0001c0004t0001g0344 | 3 | HG02717.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.864+422G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827073 | ||||||
| chr12:7827073
|
CTCTT | C | 111 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.864+418_864+421del others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827073 | ||||||
| chr12:7827087
|
CTTTCTTT others(9): Show |
C | 1 | a0003c0014t0011g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.864+392_864+407del others(16): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827087 | ||||||
| chr12:7827091
|
CTTTCTCT others(5): Show |
C | 20 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0039others(17): Show | 20 | HG00673.hp1 HG02083.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.864+392_864+403del others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827091 | ||||||
| chr12:7827093
|
T | C | 2 | a0001c0002t0003g0259a0001c0003t0001g0318 | 2 | HG01993.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.864+402A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827093 | ||||||
| chr12:7827095
|
C | CTCTT | 7 | a0001c0003t0001g0192a0001c0003t0001g0316a0001c0003t0001g0317others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+396_864+399dup others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827095 | ||||||
| chr12:7827095
|
C | CTTTCTCT others(1): Show |
37 | a0001c0004t0001g0010a0001c0004t0001g0011a0001c0004t0001g0015others(34): Show | 37 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.864+399_864+400ins others(8): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827095 | ||||||
| chr12:7827095
|
C | CTTTCTTT others(5): Show |
1 | a0001c0004t0001g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.864+399_864+400ins others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827095 | ||||||
| chr12:7827095
|
C | CTTTCTTT others(9): Show |
1 | a0001c0004t0001g0285 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.864+399_864+400ins others(16): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827095 | ||||||
| chr12:7827095
|
C | CTTTCTTT others(13): Show |
1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.864+399_864+400ins others(20): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827095 | ||||||
| chr12:7827095
|
C | T | 2 | a0001c0002t0003g0259a0001c0003t0001g0318 | 2 | HG01993.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.864+400G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827095 | ||||||
| chr12:7827099
|
T | C | 40 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0011others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.864+396A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827099 | ||||||
| chr12:7827119
|
A | C | 40 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0011others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.864+376T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827119 | ||||||
| chr12:7827137
|
T | G | 22 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0039others(19): Show | 22 | HG00673.hp1 HG01884.hp1 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.864+358A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827137 | ||||||
| chr12:7827191
|
A | G | 1 | a0001c0016t0008g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.864+304T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827191 | ||||||
| chr12:7827193
|
C | G | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+302G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827193 | ||||||
| chr12:7827252
|
C | T | 1 | a0001c0004t0001g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.864+243G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827252 | ||||||
| chr12:7827270
|
C | CT | 56 | a0001c0003t0001g0047a0001c0003t0001g0067a0001c0003t0001g0136others(53): Show | 56 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.864+224dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827270 | ||||||
| chr12:7827270
|
C | CTT | 9 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0011others(6): Show | 9 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.864+223_864+224dup others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827270 | ||||||
| chr12:7827270
|
CT | C | 135 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.864+224delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827270 | ||||||
| chr12:7827292
|
T | A | 1 | a0001c0006t0009g0284 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.864+203A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827292 | ||||||
| chr12:7827439
|
T | C | 343 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.864+56A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827439 | ||||||
| chr12:7827458
|
T | C | 15 | a0001c0005t0005g0039a0001c0008t0001g0004a0001c0008t0001g0023others(12): Show | 15 | HG00673.hp1 HG02083.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.864+37A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827458 | ||||||
| chr12:7827460
|
G | T | 15 | a0001c0005t0005g0039a0001c0008t0001g0004a0001c0008t0001g0023others(12): Show | 15 | HG00673.hp1 HG02083.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.864+35C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827460 | ||||||
| chr12:7827462
|
A | G | 5 | a0001c0002t0003g0134a0001c0002t0003g0142a0001c0002t0003g0144others(2): Show | 5 | HG01074.hp2 HG01261.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+33T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 7/10 | chr12 | 7827462 | ||||||
| chr12:7827710
|
T | TA | 347 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.677-29dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7827710 | ||||||
| chr12:7827798
|
C | A | 15 | a0001c0005t0005g0039a0001c0008t0001g0004a0001c0008t0001g0023others(12): Show | 15 | HG00673.hp1 HG02083.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.677-116G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7827798 | ||||||
| chr12:7827856
|
C | T | 76 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(73): Show | 76 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.677-174G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7827856 | ||||||
| chr12:7827894
|
A | G | 91 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(88): Show | 92 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.677-212T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7827894 | ||||||
| chr12:7827959
|
G | A | 6 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0114others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.677-277C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7827959 | ||||||
| chr12:7827963
|
G | C | 89 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(86): Show | 89 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.677-281C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7827963 | ||||||
| chr12:7827994
|
C | T | 12 | a0001c0002t0003g0055a0001c0004t0001g0009a0001c0007t0004g0019others(9): Show | 12 | HG01346.hp2 HG02280.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.677-312G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7827994 | ||||||
| chr12:7828008
|
G | A | 1 | a0002c0001t0002g0088 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.677-326C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828008 | ||||||
| chr12:7828058
|
T | TA | 15 | a0001c0005t0005g0039a0001c0008t0001g0004a0001c0008t0001g0023others(12): Show | 15 | HG00673.hp1 HG02083.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.677-377dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828058 | ||||||
| chr12:7828069
|
T | A | 25 | a0001c0004t0001g0069a0001c0004t0001g0071a0001c0004t0001g0106others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.677-387A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828069 | ||||||
| chr12:7828089
|
C | T | 1 | a0003c0014t0011g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.677-407G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828089 | ||||||
| chr12:7828271
|
A | T | 6 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0114others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.676+433T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828271 | ||||||
| chr12:7828321
|
C | T | 138 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.676+383G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828321 | ||||||
| chr12:7828364
|
CA | C | 219 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(216): Show | 220 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.676+339delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828364 | ||||||
| chr12:7828364
|
CAA | C | 104 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.676+338_676+339del others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828364 | ||||||
| chr12:7828442
|
G | A | 78 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(75): Show | 78 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.676+262C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828442 | ||||||
| chr12:7828453
|
C | G | 2 | a0001c0002t0003g0082a0001c0002t0003g0141 | 2 | HG02602.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.676+251G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828453 | ||||||
| chr12:7828474
|
A | G | 137 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.676+230T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828474 | ||||||
| chr12:7828577
|
C | T | 1 | a0003c0014t0011g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.676+127G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828577 | ||||||
| chr12:7828584
|
A | G | 8 | a0001c0006t0004g0115a0001c0006t0004g0157a0001c0006t0004g0158others(5): Show | 8 | HG02145.hp2 HG02895.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.676+120T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828584 | ||||||
| chr12:7828665
|
A | G | 1 | a0001c0007t0007g0269 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.676+39T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 6/10 | chr12 | 7828665 | ||||||
| chr12:7828945
|
G | A | 6 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0114others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.514-79C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7828945 | ||||||
| chr12:7828983
|
AAGGCTGA others(537): Show |
A | 1 | a0001c0006t0016g0273 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.513+239_514-118del | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7828983 | ||||||
| chr12:7829030
|
T | C | 138 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.514-164A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829030 | ||||||
| chr12:7829096
|
C | T | 2 | a0001c0004t0001g0285a0001c0004t0001g0344 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.514-230G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829096 | ||||||
| chr12:7829166
|
C | T | 79 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(76): Show | 79 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.514-300G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829166 | ||||||
| chr12:7829282
|
C | T | 104 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.514-416G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829282 | ||||||
| chr12:7829299
|
A | G | 104 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.514-433T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829299 | ||||||
| chr12:7829312
|
A | T | 104 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.514-446T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829312 | ||||||
| chr12:7829363
|
A | C | 104 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.513+403T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829363 | ||||||
| chr12:7829431
|
A | G | 2 | a0002c0010t0002g0049a0002c0010t0002g0050 | 2 | NA18984.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.513+335T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829431 | ||||||
| chr12:7829458
|
G | T | 104 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.513+308C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829458 | ||||||
| chr12:7829503
|
C | T | 1 | a0001c0003t0001g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.513+263G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829503 | ||||||
| chr12:7829554
|
CA | C | 218 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(215): Show | 219 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.513+211delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829554 | ||||||
| chr12:7829562
|
A | G | 104 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.513+204T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829562 | ||||||
| chr12:7829762
|
G | C | 1 | a0003c0014t0011g0102 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.513+4C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 5/10 | chr12 | 7829762 | ||||||
| chr12:7830129
|
T | C | 2 | a0001c0007t0009g0078a0001c0007t0009g0291 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.273-123A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830129 | ||||||
| chr12:7830157
|
CT | C | 238 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.273-152delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830157 | ||||||
| chr12:7830157
|
CTT | C | 84 | a0001c0004t0001g0127a0001c0004t0001g0268a0001c0004t0001g0339others(81): Show | 85 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.273-153_273-152del others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830157 | ||||||
| chr12:7830183
|
C | T | 33 | a0001c0004t0001g0011a0001c0004t0001g0069a0001c0004t0001g0071others(30): Show | 33 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.273-177G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830183 | ||||||
| chr12:7830208
|
A | C | 4 | a0001c0004t0001g0185a0001c0004t0001g0266a0001c0004t0001g0343others(1): Show | 4 | HG02965.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-202T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830208 | ||||||
| chr12:7830288
|
A | G | 1 | a0002c0001t0002g0214 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.273-282T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830288 | ||||||
| chr12:7830318
|
A | AT | 4 | a0001c0003t0001g0024a0001c0003t0001g0047a0001c0003t0001g0083others(1): Show | 4 | HG02027.hp1 HG02155.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-313dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830318 | ||||||
| chr12:7830344
|
G | A | 80 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(77): Show | 80 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.273-338C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830344 | ||||||
| chr12:7830498
|
T | G | 3 | a0001c0004t0001g0326a0001c0005t0005g0319a0001c0005t0005g0327 | 3 | HG02572.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.273-492A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830498 | ||||||
| chr12:7830569
|
G | A | 2 | a0002c0011t0008g0003a0002c0011t0008g0289 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.273-563C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830569 | ||||||
| chr12:7830716
|
T | C | 342 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(339): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.273-710A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830716 | ||||||
| chr12:7830779
|
A | T | 1 | a0001c0003t0001g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.273-773T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830779 | ||||||
| chr12:7830806
|
T | C | 2 | a0001c0004t0001g0339a0002c0001t0002g0002 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.272+798A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830806 | ||||||
| chr12:7830882
|
A | G | 330 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.272+722T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830882 | ||||||
| chr12:7830898
|
C | T | 6 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0114others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.272+706G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830898 | ||||||
| chr12:7830908
|
A | G | 104 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.272+696T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7830908 | ||||||
| chr12:7831099
|
A | G | 347 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.272+505T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831099 | ||||||
| chr12:7831124
|
C | CAA | 102 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(99): Show | 103 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.272+478_272+479dup others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831124 | ||||||
| chr12:7831124
|
CA | C | 8 | a0001c0003t0001g0068a0001c0004t0001g0197a0001c0005t0005g0213others(5): Show | 8 | HG00323.hp1 HG01496.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.272+479delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831124 | ||||||
| chr12:7831214
|
T | C | 1 | a0001c0002t0003g0128 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.272+390A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831214 | ||||||
| chr12:7831240
|
G | A | 1 | a0001c0005t0005g0327 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.272+364C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831240 | ||||||
| chr12:7831252
|
GT | G | 26 | a0001c0002t0003g0055a0001c0002t0003g0148a0001c0004t0001g0007others(23): Show | 26 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.272+351delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831252 | ||||||
| chr12:7831252
|
GTT | G | 314 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(311): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.272+350_272+351del others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831252 | ||||||
| chr12:7831258
|
T | G | 2 | a0001c0004t0001g0285a0001c0004t0001g0344 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.272+346A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831258 | ||||||
| chr12:7831294
|
T | C | 1 | a0001c0005t0005g0120 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.272+310A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831294 | ||||||
| chr12:7831317
|
C | A | 1 | a0003c0012t0011g0113 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.272+287G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831317 | ||||||
| chr12:7831421
|
C | A | 347 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.272+183G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831421 | ||||||
| chr12:7831469
|
T | C | 2 | a0001c0004t0001g0127a0001c0004t0001g0268 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.272+135A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831469 | ||||||
| chr12:7831559
|
T | C | 1 | a0001c0006t0004g0246 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.272+45A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 4/10 | chr12 | 7831559 | ||||||
| chr12:7831851
|
G | A | 122 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0011others(119): Show | 123 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.112-87C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 3/10 | chr12 | 7831851 | ||||||
| chr12:7831880
|
G | T | 2 | a0002c0011t0008g0003a0002c0011t0008g0289 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.112-116C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 3/10 | chr12 | 7831880 | ||||||
| chr12:7832091
|
G | C | 1 | a0001c0004t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.112-327C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 3/10 | chr12 | 7832091 | ||||||
| chr12:7832175
|
A | G | 1 | a0001c0007t0009g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.112-411T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 3/10 | chr12 | 7832175 | ||||||
| chr12:7832278
|
G | A | 121 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0011others(118): Show | 122 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.111+444C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 3/10 | chr12 | 7832278 | ||||||
| chr12:7832345
|
C | T | 34 | a0001c0003t0001g0320a0001c0004t0001g0011a0001c0004t0001g0069others(31): Show | 34 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.111+377G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 3/10 | chr12 | 7832345 | ||||||
| chr12:7832352
|
T | C | 2 | a0001c0004t0001g0285a0001c0004t0001g0344 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.111+370A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 3/10 | chr12 | 7832352 | ||||||
| chr12:7832362
|
T | C | 1 | a0001c0002t0003g0196 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.111+360A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 3/10 | chr12 | 7832362 | ||||||
| chr12:7832571
|
G | A | 1 | a0002c0001t0002g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.111+151C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 3/10 | chr12 | 7832571 | ||||||
| chr12:7832599
|
C | A | 8 | a0001c0003t0001g0192a0001c0003t0001g0316a0001c0003t0001g0317others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+123G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 3/10 | chr12 | 7832599 | ||||||
| chr12:7832855
|
A | G | 1 | a0002c0001t0002g0299 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.19-41T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7832855 | ||||||
| chr12:7832864
|
T | C | 36 | a0001c0004t0001g0011a0001c0004t0001g0069a0001c0004t0001g0071others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.19-50A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7832864 | ||||||
| chr12:7832871
|
C | T | 1 | a0001c0005t0005g0336 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-57G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7832871 | ||||||
| chr12:7832965
|
G | A | 1 | a0001c0007t0007g0269 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19-151C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7832965 | ||||||
| chr12:7833155
|
A | G | 227 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(224): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.19-341T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833155 | ||||||
| chr12:7833156
|
A | C | 227 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(224): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.19-342T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833156 | ||||||
| chr12:7833262
|
G | A | 1 | a0002c0001t0002g0253 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.19-448C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833262 | ||||||
| chr12:7833450
|
C | T | 113 | a0001c0004t0001g0011a0001c0004t0001g0069a0001c0004t0001g0071others(110): Show | 114 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.19-636G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833450 | ||||||
| chr12:7833618
|
T | G | 39 | a0001c0004t0001g0011a0001c0004t0001g0069a0001c0004t0001g0071others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.19-804A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833618 | ||||||
| chr12:7833637
|
A | C | 323 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(320): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.19-823T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833637 | ||||||
| chr12:7833637
|
A | T | 24 | a0001c0003t0010g0013a0001c0003t0010g0014a0001c0003t0010g0098others(21): Show | 24 | HG00673.hp1 HG01952.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.19-823T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833637 | ||||||
| chr12:7833638
|
G | A | 2 | a0001c0004t0001g0009a0001c0007t0018g0346 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.19-824C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833638 | ||||||
| chr12:7833647
|
G | T | 5 | a0001c0002t0003g0091a0001c0002t0003g0092a0001c0002t0003g0093others(2): Show | 5 | HG00099.hp1 HG00642.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-833C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833647 | ||||||
| chr12:7833713
|
C | T | 1 | a0001c0002t0003g0066 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.19-899G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833713 | ||||||
| chr12:7833781
|
C | CA | 12 | a0001c0003t0001g0047a0001c0003t0001g0313a0001c0003t0001g0314others(9): Show | 12 | HG01346.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.19-968dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833781 | ||||||
| chr12:7833795
|
A | AAG | 144 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.19-983_19-982dupCT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833795 | ||||||
| chr12:7833795
|
A | AG | 80 | a0001c0002t0003g0278a0001c0004t0001g0007a0001c0004t0001g0010others(77): Show | 81 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.19-982_19-981insC | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833795 | ||||||
| chr12:7833795
|
A | G | 2 | a0002c0001t0002g0179a0002c0001t0002g0299 | 2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.19-981T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833795 | ||||||
| chr12:7833953
|
C | G | 1 | a0001c0003t0001g0060 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.19-1139G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833953 | ||||||
| chr12:7833967
|
C | A | 225 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.19-1153G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7833967 | ||||||
| chr12:7834054
|
CT | C | 108 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.19-1241delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7834054 | ||||||
| chr12:7834054
|
CTCTCAGA others(5): Show |
C | 1 | a0002c0001t0002g0160 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.19-1252_19-1241del others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7834054 | ||||||
| chr12:7834188
|
C | CT | 6 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0114others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-1375dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7834188 | ||||||
| chr12:7834443
|
CT | C | 5 | a0001c0002t0003g0091a0001c0002t0003g0092a0001c0002t0003g0093others(2): Show | 5 | HG00099.hp1 HG00642.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-1630delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7834443 | ||||||
| chr12:7834530
|
C | CT | 79 | a0001c0004t0001g0009a0001c0004t0001g0326a0001c0004t0001g0339others(76): Show | 80 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.19-1717dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7834530 | ||||||
| chr12:7834530
|
CT | C | 229 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.19-1717delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7834530 | ||||||
| chr12:7834532
|
T | C | 8 | a0001c0003t0001g0313a0001c0004t0001g0254a0001c0005t0005g0008others(5): Show | 8 | HG01981.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-1718A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7834532 | ||||||
| chr12:7834563
|
CA | C | 166 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.19-1750delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7834563 | ||||||
| chr12:7834563
|
CAA | C | 103 | a0001c0002t0003g0044a0001c0002t0003g0066a0001c0002t0003g0079others(100): Show | 103 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.19-1751_19-1750del others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7834563 | ||||||
| chr12:7834721
|
G | GA | 117 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0011others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.19-1908dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7834721 | ||||||
| chr12:7834778
|
A | G | 1 | a0002c0001t0002g0155 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.19-1964T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7834778 | ||||||
| chr12:7834886
|
C | T | 1 | a0001c0003t0001g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.19-2072G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7834886 | ||||||
| chr12:7835093
|
G | T | 347 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.19-2279C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7835093 | ||||||
| chr12:7835100
|
TA | T | 115 | a0001c0003t0001g0298a0001c0003t0001g0303a0001c0004t0001g0011others(112): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.19-2287delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7835100 | ||||||
| chr12:7835165
|
G | A | 97 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(94): Show | 97 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.19-2351C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7835165 | ||||||
| chr12:7835195
|
T | C | 2 | a0002c0011t0008g0003a0002c0011t0008g0289 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.19-2381A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7835195 | ||||||
| chr12:7835238
|
T | G | 1 | a0001c0004t0001g0348 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.19-2424A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7835238 | ||||||
| chr12:7835285
|
A | G | 338 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.19-2471T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7835285 | ||||||
| chr12:7835335
|
C | T | 1 | a0001c0003t0001g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.19-2521G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7835335 | ||||||
| chr12:7835344
|
G | A | 117 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0011others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.19-2530C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7835344 | ||||||
| chr12:7835793
|
G | A | 3 | a0001c0004t0001g0326a0001c0005t0005g0319a0001c0005t0005g0327 | 3 | HG02572.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.19-2979C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7835793 | ||||||
| chr12:7835814
|
G | T | 6 | a0001c0004t0001g0285a0001c0004t0001g0326a0001c0004t0001g0344others(3): Show | 6 | HG02572.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-3000C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7835814 | ||||||
| chr12:7836037
|
G | A | 1 | a0001c0003t0001g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.19-3223C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7836037 | ||||||
| chr12:7836194
|
T | G | 1 | a0001c0002t0003g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.19-3380A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7836194 | ||||||
| chr12:7836219
|
A | G | 341 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(338): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.19-3405T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7836219 | ||||||
| chr12:7836223
|
C | CT | 305 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(302): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.19-3410dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7836223 | ||||||
| chr12:7836223
|
C | CTT | 35 | a0001c0002t0003g0256a0001c0005t0005g0033a0001c0005t0005g0061others(32): Show | 35 | HG00408.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.19-3411_19-3410dup others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7836223 | ||||||
| chr12:7836263
|
C | T | 117 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0011others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.19-3449G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7836263 | ||||||
| chr12:7836492
|
T | C | 1 | a0001c0008t0001g0239 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.19-3678A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7836492 | ||||||
| chr12:7836679
|
C | G | 98 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(95): Show | 98 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.19-3865G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7836679 | ||||||
| chr12:7836807
|
G | A | 2 | a0001c0002t0003g0079a0001c0002t0003g0259 | 2 | HG01993.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.19-3993C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7836807 | ||||||
| chr12:7836934
|
T | C | 322 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.19-4120A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7836934 | ||||||
| chr12:7836957
|
A | G | 16 | a0001c0005t0005g0039a0001c0008t0001g0004a0001c0008t0001g0023others(13): Show | 16 | HG00673.hp1 HG02083.hp2 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.19-4143T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7836957 | ||||||
| chr12:7837037
|
C | T | 1 | a0001c0004t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.19-4223G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837037 | ||||||
| chr12:7837038
|
A | G | 347 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.19-4224T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837038 | ||||||
| chr12:7837059
|
C | T | 2 | a0001c0006t0009g0081a0001c0006t0009g0284 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.19-4245G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837059 | ||||||
| chr12:7837060
|
G | A | 2 | a0002c0011t0008g0003a0002c0011t0008g0289 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.19-4246C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837060 | ||||||
| chr12:7837143
|
G | A | 1 | a0001c0003t0001g0083 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.19-4329C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837143 | ||||||
| chr12:7837166
|
C | CA | 11 | a0001c0003t0001g0192a0001c0003t0001g0316a0001c0003t0001g0317others(8): Show | 11 | HG00438.hp1 HG01891.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-4353dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837166 | ||||||
| chr12:7837204
|
G | A | 5 | a0001c0003t0010g0013a0001c0003t0010g0014a0001c0003t0010g0098others(2): Show | 5 | HG01952.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-4390C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837204 | ||||||
| chr12:7837268
|
TTTTA | T | 16 | a0001c0005t0005g0039a0001c0008t0001g0004a0001c0008t0001g0023others(13): Show | 16 | HG00673.hp1 HG02083.hp2 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.19-4458_19-4455del others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837268 | ||||||
| chr12:7837292
|
T | C | 2 | a0002c0011t0008g0003a0002c0011t0008g0289 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.19-4478A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837292 | ||||||
| chr12:7837372
|
C | T | 25 | a0001c0004t0001g0069a0001c0004t0001g0071a0001c0004t0001g0106others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.19-4558G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837372 | ||||||
| chr12:7837415
|
G | A | 115 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.19-4601C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837415 | ||||||
| chr12:7837578
|
C | T | 1 | a0001c0005t0005g0120 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.19-4764G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837578 | ||||||
| chr12:7837579
|
A | G | 336 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(333): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.19-4765T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837579 | ||||||
| chr12:7837638
|
C | CAAAAAAA | 54 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.19-4831_19-4825dup others(7): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837638
|
C | CAAAAAAA others(1): Show |
116 | a0001c0002t0003g0055a0001c0002t0003g0066a0001c0002t0003g0085others(113): Show | 117 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.19-4832_19-4825dup others(8): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837638
|
C | CAAAAAAA others(2): Show |
61 | a0001c0002t0003g0279a0001c0004t0001g0011a0001c0004t0001g0071others(58): Show | 61 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.19-4833_19-4825dup others(9): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837638
|
C | CAAAAAAA others(3): Show |
18 | a0001c0004t0001g0009a0001c0004t0001g0069a0001c0004t0001g0109others(15): Show | 18 | HG00280.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.19-4834_19-4825dup others(10): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837638
|
C | CAAAAAAA others(4): Show |
5 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-4835_19-4825dup others(11): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837638
|
C | CAAAAAAA others(5): Show |
2 | a0001c0003t0001g0018a0001c0003t0010g0098 | 2 | HG01952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.19-4836_19-4825dup others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837638
|
C | CAAAAAAA others(6): Show |
6 | a0001c0003t0001g0221a0001c0003t0010g0013a0001c0003t0010g0014others(3): Show | 6 | HG02155.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-4837_19-4825dup others(13): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837638
|
C | CAAAAAAA others(7): Show |
34 | a0001c0003t0001g0028a0001c0003t0001g0042a0001c0003t0001g0056others(31): Show | 34 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.19-4838_19-4825dup others(14): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837638
|
C | CAAAAAAA others(8): Show |
30 | a0001c0003t0001g0024a0001c0003t0001g0047a0001c0003t0001g0058others(27): Show | 30 | HG01891.hp1 HG01981.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.19-4839_19-4825dup others(15): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837638
|
C | CAAAAAAA others(9): Show |
6 | a0001c0003t0001g0186a0001c0003t0001g0316a0001c0003t0001g0318others(3): Show | 6 | HG02145.hp2 HG02572.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-4840_19-4825dup others(16): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837638
|
C | CAAAAAAA others(10): Show |
1 | a0001c0003t0001g0153 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.19-4841_19-4825dup others(17): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837638
|
C | CAAAAAAA others(11): Show |
1 | a0001c0006t0004g0158 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.19-4842_19-4825dup others(18): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837638
|
C | CCAAAAAA others(1): Show |
6 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0114others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-4825_19-4824ins others(8): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837638 | ||||||
| chr12:7837657
|
G | A | 1 | a0002c0001t0002g0160 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.19-4843C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837657 | ||||||
| chr12:7837667
|
A | G | 1 | a0001c0003t0010g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.19-4853T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837667 | ||||||
| chr12:7837685
|
CT | C | 343 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.19-4872delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837685 | ||||||
| chr12:7837775
|
C | T | 340 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.19-4961G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837775 | ||||||
| chr12:7837836
|
C | T | 310 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.19-5022G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837836 | ||||||
| chr12:7837853
|
G | A | 7 | a0001c0003t0001g0313a0001c0004t0001g0254a0001c0005t0005g0008others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-5039C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837853 | ||||||
| chr12:7837858
|
A | G | 1 | a0002c0001t0002g0295 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.19-5044T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837858 | ||||||
| chr12:7837878
|
C | T | 2 | a0001c0007t0004g0203a0001c0007t0004g0204 | 2 | NA18962.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.19-5064G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837878 | ||||||
| chr12:7837993
|
G | C | 1 | a0002c0001t0002g0133 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.19-5179C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7837993 | ||||||
| chr12:7838009
|
C | T | 1 | a0002c0001t0002g0309 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.19-5195G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838009 | ||||||
| chr12:7838093
|
AT | A | 37 | a0001c0004t0001g0011a0001c0004t0001g0069a0001c0004t0001g0071others(34): Show | 37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.19-5280delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838093 | ||||||
| chr12:7838122
|
C | T | 6 | a0001c0004t0001g0285a0001c0004t0001g0326a0001c0004t0001g0344others(3): Show | 6 | HG02572.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-5308G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838122 | ||||||
| chr12:7838139
|
G | A | 2 | a0002c0011t0008g0003a0002c0011t0008g0289 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.19-5325C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838139 | ||||||
| chr12:7838155
|
T | C | 2 | a0001c0004t0001g0285a0001c0004t0001g0344 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.19-5341A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838155 | ||||||
| chr12:7838232
|
C | T | 3 | a0001c0004t0001g0011a0001c0004t0001g0183a0001c0004t0001g0184 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.19-5418G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838232 | ||||||
| chr12:7838355
|
G | A | 1 | a0001c0002t0003g0302 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.19-5541C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838355 | ||||||
| chr12:7838376
|
G | T | 2 | a0001c0004t0001g0266a0001c0004t0001g0343 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.19-5562C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838376 | ||||||
| chr12:7838381
|
C | G | 81 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(78): Show | 81 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.19-5567G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838381 | ||||||
| chr12:7838398
|
T | A | 118 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.19-5584A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838398 | ||||||
| chr12:7838404
|
A | G | 8 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(5): Show | 8 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-5590T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838404 | ||||||
| chr12:7838491
|
T | G | 2 | a0001c0004t0001g0009a0001c0007t0018g0346 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.19-5677A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838491 | ||||||
| chr12:7838579
|
T | G | 6 | a0001c0006t0004g0035a0001c0006t0004g0051a0001c0006t0004g0073others(3): Show | 6 | HG01496.hp2 HG01943.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-5765A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838579 | ||||||
| chr12:7838607
|
C | T | 1 | a0001c0003t0001g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.19-5793G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838607 | ||||||
| chr12:7838662
|
T | A | 8 | a0001c0006t0004g0115a0001c0006t0004g0157a0001c0006t0004g0158others(5): Show | 8 | HG02145.hp2 HG02895.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-5848A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838662 | ||||||
| chr12:7838796
|
G | A | 1 | a0002c0001t0002g0253 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.19-5982C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838796 | ||||||
| chr12:7838841
|
A | G | 1 | a0001c0005t0006g0170 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.19-6027T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838841 | ||||||
| chr12:7838863
|
A | G | 1 | a0001c0005t0006g0170 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.19-6049T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838863 | ||||||
| chr12:7838888
|
C | A | 14 | a0001c0004t0001g0009a0001c0005t0005g0039a0001c0007t0018g0346others(11): Show | 14 | HG00673.hp1 HG02083.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.19-6074G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838888 | ||||||
| chr12:7838917
|
G | A | 42 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(39): Show | 42 | HG00544.hp1 HG00609.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.19-6103C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7838917 | ||||||
| chr12:7839195
|
G | A | 1 | a0001c0002t0003g0126 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.19-6381C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839195 | ||||||
| chr12:7839230
|
G | A | 78 | a0001c0003t0001g0130a0001c0003t0001g0225a0001c0003t0001g0226others(75): Show | 79 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.19-6416C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839230 | ||||||
| chr12:7839267
|
C | A | 2 | a0001c0004t0001g0009a0001c0007t0018g0346 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.19-6453G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839267 | ||||||
| chr12:7839312
|
G | C | 292 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(289): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.19-6498C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839312 | ||||||
| chr12:7839321
|
A | G | 118 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.19-6507T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839321 | ||||||
| chr12:7839391
|
C | T | 2 | a0001c0005t0005g0249a0002c0001t0002g0199 | 2 | NA18970.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.19-6577G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839391 | ||||||
| chr12:7839452
|
A | G | 5 | a0001c0003t0001g0135a0001c0003t0001g0136a0002c0001t0002g0179others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-6638T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839452 | ||||||
| chr12:7839576
|
C | G | 24 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(21): Show | 24 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.19-6762G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839576 | ||||||
| chr12:7839594
|
A | G | 4 | a0001c0004t0001g0185a0001c0004t0001g0266a0001c0004t0001g0343others(1): Show | 4 | HG02965.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-6780T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839594 | ||||||
| chr12:7839671
|
A | C | 214 | a0001c0002t0003g0257a0001c0002t0003g0258a0001c0002t0003g0302others(211): Show | 215 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.19-6857T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839671 | ||||||
| chr12:7839696
|
A | G | 347 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.19-6882T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839696 | ||||||
| chr12:7839819
|
A | G | 1 | a0002c0001t0002g0300 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.19-7005T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839819 | ||||||
| chr12:7839844
|
C | T | 119 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.19-7030G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839844 | ||||||
| chr12:7839924
|
CA | C | 79 | a0001c0002t0003g0021a0001c0002t0003g0022a0001c0002t0003g0031others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.19-7111delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839924 | ||||||
| chr12:7839924
|
CAAA | C | 9 | a0001c0003t0010g0013a0001c0003t0010g0014a0001c0003t0010g0098others(6): Show | 9 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-7113_19-7111del others(3): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839924 | ||||||
| chr12:7839924
|
CAAAA | C | 11 | a0001c0002t0003g0337a0001c0004t0001g0118a0001c0004t0001g0171others(8): Show | 11 | HG00642.hp1 HG01123.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-7114_19-7111del others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839924 | ||||||
| chr12:7839924
|
CAAAAA | C | 32 | a0001c0002t0003g0257a0001c0002t0003g0258a0001c0002t0003g0302others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.19-7115_19-7111del others(5): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839924 | ||||||
| chr12:7839924
|
CAAAAAAA others(3): Show |
C | 12 | a0001c0004t0001g0009a0001c0005t0005g0039a0001c0007t0018g0346others(9): Show | 12 | HG00673.hp1 HG02083.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.19-7120_19-7111del others(10): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839924 | ||||||
| chr12:7839924
|
CAAAAAAA others(4): Show |
C | 17 | a0001c0003t0001g0047a0001c0003t0001g0218a0001c0003t0001g0225others(14): Show | 17 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-7121_19-7111del others(11): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839924 | ||||||
| chr12:7839924
|
CAAAAAAA others(5): Show |
C | 138 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(135): Show | 139 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.19-7122_19-7111del others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839924 | ||||||
| chr12:7839945
|
A | T | 1 | a0002c0001t0002g0149 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.19-7131T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839945 | ||||||
| chr12:7839947
|
A | C | 1 | a0002c0001t0002g0149 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.19-7133T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839947 | ||||||
| chr12:7839953
|
A | T | 1 | a0002c0001t0002g0124 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.19-7139T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839953 | ||||||
| chr12:7839954
|
T | A | 1 | a0001c0005t0005g0120 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.19-7140A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7839954 | ||||||
| chr12:7840055
|
T | C | 1 | a0001c0005t0006g0170 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.19-7241A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840055 | ||||||
| chr12:7840111
|
C | CA | 88 | a0001c0002t0003g0279a0001c0002t0003g0293a0001c0003t0001g0130others(85): Show | 89 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.19-7298dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840111 | ||||||
| chr12:7840111
|
C | CAA | 32 | a0001c0003t0001g0117a0001c0003t0001g0135a0001c0003t0001g0136others(29): Show | 32 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.19-7299_19-7298dup others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840111 | ||||||
| chr12:7840111
|
C | CAAA | 43 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(40): Show | 43 | HG00544.hp1 HG00609.hp2 HG01496.hp2 others(40): Show |
intron_variant | MODIFIER | c.19-7300_19-7298dup others(3): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840111 | ||||||
| chr12:7840111
|
C | CAAAA | 6 | a0001c0003t0001g0067a0001c0003t0001g0218a0001c0006t0004g0035others(3): Show | 6 | HG01981.hp1 NA18948.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-7301_19-7298dup others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840111 | ||||||
| chr12:7840111
|
CA | C | 26 | a0001c0003t0001g0313a0001c0003t0010g0013a0001c0003t0010g0014others(23): Show | 26 | HG00738.hp1 HG01109.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.19-7298delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840111 | ||||||
| chr12:7840160
|
CT | C | 183 | a0001c0002t0003g0020a0001c0002t0003g0055a0001c0002t0003g0079others(180): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.19-7347delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840160 | ||||||
| chr12:7840160
|
CTT | C | 15 | a0001c0004t0001g0254a0001c0004t0001g0268a0001c0004t0001g0285others(12): Show | 15 | HG02258.hp2 HG02451.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.19-7348_19-7347del others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840160 | ||||||
| chr12:7840160
|
CTTTTTTT others(6): Show |
C | 36 | a0001c0002t0003g0257a0001c0002t0003g0258a0001c0002t0003g0302others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.19-7359_19-7347del others(13): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840160 | ||||||
| chr12:7840181
|
T | C | 6 | a0001c0004t0001g0254a0001c0005t0005g0008a0001c0005t0005g0114others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-7367A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840181 | ||||||
| chr12:7840224
|
G | T | 36 | a0001c0002t0003g0257a0001c0002t0003g0258a0001c0002t0003g0302others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.19-7410C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840224 | ||||||
| chr12:7840240
|
C | T | 1 | a0001c0004t0001g0343 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-7426G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840240 | ||||||
| chr12:7840299
|
G | A | 3 | a0001c0002t0003g0277a0001c0002t0003g0278a0001c0002t0003g0279 | 3 | NA19072.hp2 NA19090.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.19-7485C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840299 | ||||||
| chr12:7840440
|
C | A | 13 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(10): Show | 13 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.19-7626G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840440 | ||||||
| chr12:7840532
|
A | ACCACAC | 13 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(10): Show | 13 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.19-7724_19-7719dup others(6): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840532 | ||||||
| chr12:7840665
|
C | T | 1 | a0001c0003t0001g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.19-7851G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840665 | ||||||
| chr12:7840704
|
C | T | 2 | a0001c0004t0001g0267a0001c0004t0001g0304 | 2 | HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.19-7890G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840704 | ||||||
| chr12:7840720
|
A | C | 80 | a0001c0002t0003g0082a0001c0002t0003g0141a0001c0003t0001g0130others(77): Show | 81 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.19-7906T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840720 | ||||||
| chr12:7840957
|
C | T | 3 | a0001c0002t0003g0134a0001c0002t0003g0142a0001c0002t0003g0260 | 3 | HG01074.hp2 HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.19-8143G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840957 | ||||||
| chr12:7840974
|
T | TA | 90 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(87): Show | 90 | HG00544.hp1 HG00609.hp2 HG01496.hp2 others(87): Show |
intron_variant | MODIFIER | c.19-8161dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7840974 | ||||||
| chr12:7841003
|
C | G | 1 | a0002c0001t0002g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.19-8189G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7841003 | ||||||
| chr12:7841330
|
G | A | 72 | a0001c0003t0001g0130a0001c0003t0001g0225a0001c0003t0001g0226others(69): Show | 73 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.19-8516C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7841330 | ||||||
| chr12:7841396
|
G | C | 3 | a0001c0005t0005g0335a0001c0005t0005g0336a0001c0005t0005g0338 | 3 | HG01123.hp2 HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.19-8582C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7841396 | ||||||
| chr12:7841435
|
A | G | 1 | a0001c0003t0001g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.19-8621T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7841435 | ||||||
| chr12:7841496
|
G | C | 7 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-8682C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7841496 | ||||||
| chr12:7841540
|
C | T | 1 | a0001c0007t0009g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.19-8726G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7841540 | ||||||
| chr12:7841773
|
C | T | 9 | a0001c0004t0001g0236a0001c0004t0001g0237a0001c0004t0001g0248others(6): Show | 9 | HG00738.hp1 HG02486.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-8959G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7841773 | ||||||
| chr12:7841774
|
A | G | 9 | a0001c0004t0001g0236a0001c0004t0001g0237a0001c0004t0001g0248others(6): Show | 9 | HG00738.hp1 HG02486.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-8960T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7841774 | ||||||
| chr12:7841905
|
T | C | 2 | a0001c0003t0001g0314a0002c0013t0002g0182 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.19-9091A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7841905 | ||||||
| chr12:7841930
|
A | G | 290 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.19-9116T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7841930 | ||||||
| chr12:7841960
|
G | C | 47 | a0001c0003t0001g0018a0001c0003t0001g0024a0001c0003t0001g0028others(44): Show | 47 | HG00544.hp1 HG00609.hp2 HG01496.hp2 others(44): Show |
intron_variant | MODIFIER | c.19-9146C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7841960 | ||||||
| chr12:7842010
|
G | GA | 7 | a0001c0003t0001g0313a0001c0004t0001g0326a0001c0004t0001g0344others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-9197dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842010 | ||||||
| chr12:7842138
|
T | C | 4 | a0001c0004t0001g0268a0001c0006t0004g0286a0001c0006t0004g0287others(1): Show | 4 | HG02965.hp2 HG03579.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-9324A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842138 | ||||||
| chr12:7842142
|
T | G | 1 | a0001c0004t0001g0326 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.19-9328A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842142 | ||||||
| chr12:7842162
|
G | A | 1 | a0001c0004t0001g0326 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.19-9348C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842162 | ||||||
| chr12:7842195
|
C | T | 1 | a0001c0004t0001g0326 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.19-9381G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842195 | ||||||
| chr12:7842196
|
C | T | 2 | a0002c0001t0002g0162a0002c0001t0002g0251 | 2 | NA18990.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.19-9382G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842196 | ||||||
| chr12:7842401
|
T | C | 2 | a0002c0011t0008g0003a0002c0011t0008g0289 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.19-9587A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842401 | ||||||
| chr12:7842433
|
A | G | 1 | a0001c0004t0001g0326 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.19-9619T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842433 | ||||||
| chr12:7842468
|
G | A | 5 | a0001c0004t0001g0007a0001c0004t0001g0010a0001c0004t0001g0015others(2): Show | 5 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-9654C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842468 | ||||||
| chr12:7842476
|
A | T | 2 | a0001c0004t0001g0326a0001c0007t0004g0027 | 2 | HG02615.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.19-9662T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842476 | ||||||
| chr12:7842477
|
C | G | 1 | a0001c0007t0004g0027 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.19-9663G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842477 | ||||||
| chr12:7842614
|
C | T | 2 | a0001c0002t0003g0142a0001c0002t0003g0260 | 2 | HG01074.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.19-9800G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842614 | ||||||
| chr12:7842645
|
C | A | 1 | a0002c0001t0002g0276 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.19-9831G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842645 | ||||||
| chr12:7842722
|
CT | C | 105 | a0001c0002t0003g0082a0001c0002t0003g0119a0001c0002t0003g0302others(102): Show | 106 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.19-9909delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842722 | ||||||
| chr12:7842736
|
T | G | 1 | a0001c0003t0001g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.19-9922A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842736 | ||||||
| chr12:7842737
|
G | T | 1 | a0001c0003t0001g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.19-9923C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842737 | ||||||
| chr12:7842781
|
T | A | 6 | a0001c0004t0001g0096a0001c0004t0001g0097a0001c0004t0001g0254others(3): Show | 6 | HG00639.hp1 HG01257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-9967A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842781 | ||||||
| chr12:7842814
|
C | T | 1 | a0001c0005t0005g0338 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.19-10000G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842814 | ||||||
| chr12:7842854
|
G | A | 107 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.19-10040C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842854 | ||||||
| chr12:7842951
|
C | A | 1 | a0001c0004t0001g0069 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.19-10137G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7842951 | ||||||
| chr12:7843047
|
G | A | 3 | a0001c0005t0005g0335a0001c0005t0005g0336a0001c0005t0005g0338 | 3 | HG01123.hp2 HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.19-10233C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843047 | ||||||
| chr12:7843049
|
C | A | 3 | a0001c0004t0001g0009a0001c0004t0001g0344a0001c0007t0018g0346 | 3 | HG02280.hp1 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.19-10235G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843049 | ||||||
| chr12:7843054
|
A | G | 85 | a0001c0002t0003g0066a0001c0002t0003g0100a0001c0003t0001g0018others(82): Show | 85 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.19-10240T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843054 | ||||||
| chr12:7843116
|
G | A | 1 | a0001c0006t0009g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-10302C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843116 | ||||||
| chr12:7843176
|
G | T | 3 | a0001c0004t0001g0011a0001c0004t0001g0183a0001c0004t0001g0184 | 3 | HG02647.hp1 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.19-10362C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843176 | ||||||
| chr12:7843198
|
C | CT | 55 | a0001c0002t0003g0031a0001c0002t0003g0082a0001c0002t0003g0091others(52): Show | 55 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.19-10385dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843198 | ||||||
| chr12:7843258
|
C | T | 3 | a0001c0004t0001g0296a0001c0004t0001g0297a0001c0007t0018g0346 | 3 | HG01168.hp2 HG01169.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.19-10444G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843258 | ||||||
| chr12:7843268
|
G | A | 7 | a0001c0004t0001g0007a0001c0004t0001g0009a0001c0004t0001g0010others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-10454C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843268 | ||||||
| chr12:7843272
|
G | A | 95 | a0001c0002t0003g0031a0001c0002t0003g0079a0001c0002t0003g0085others(92): Show | 95 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.19-10458C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843272 | ||||||
| chr12:7843319
|
T | C | 187 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.19-10505A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843319 | ||||||
| chr12:7843376
|
A | G | 8 | a0001c0004t0001g0007a0001c0004t0001g0009a0001c0004t0001g0010others(5): Show | 8 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-10562T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843376 | ||||||
| chr12:7843402
|
G | T | 2 | a0001c0002t0003g0082a0001c0004t0001g0332 | 2 | HG03139.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.19-10588C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843402 | ||||||
| chr12:7843420
|
A | G | 7 | a0001c0004t0001g0315a0001c0005t0005g0319a0001c0005t0005g0327others(4): Show | 7 | HG02572.hp1 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-10606T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843420 | ||||||
| chr12:7843534
|
AC | A | 65 | a0001c0002t0003g0079a0001c0002t0003g0090a0001c0002t0003g0091others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.19-10721delG | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843534 | ||||||
| chr12:7843537
|
C | T | 17 | a0001c0003t0001g0272a0001c0004t0001g0007a0001c0004t0001g0009others(14): Show | 17 | HG00639.hp1 HG01109.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-10723G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843537 | ||||||
| chr12:7843540
|
C | T | 1 | a0001c0004t0001g0333 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-10726G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843540 | ||||||
| chr12:7843555
|
T | G | 1 | a0001c0007t0009g0078 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.19-10741A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843555 | ||||||
| chr12:7843650
|
C | T | 1 | a0002c0009t0002g0052 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.19-10836G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843650 | ||||||
| chr12:7843651
|
G | GA | 7 | a0001c0002t0003g0044a0001c0003t0001g0136a0001c0003t0001g0153others(4): Show | 7 | HG00408.hp2 HG00423.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-10838dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843651 | ||||||
| chr12:7843786
|
G | A | 1 | a0001c0005t0006g0165 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.19-10972C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843786 | ||||||
| chr12:7843806
|
G | A | 284 | a0001c0002t0003g0020a0001c0002t0003g0022a0001c0002t0003g0031others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.19-10992C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843806 | ||||||
| chr12:7843807
|
G | A | 105 | a0001c0002t0003g0053a0001c0002t0003g0085a0001c0002t0003g0256others(102): Show | 105 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.19-10993C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843807 | ||||||
| chr12:7843874
|
G | A | 132 | a0001c0002t0003g0041a0001c0002t0003g0053a0001c0002t0003g0054others(129): Show | 133 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.19-11060C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843874 | ||||||
| chr12:7843896
|
G | GA | 10 | a0001c0002t0003g0021a0001c0004t0001g0069a0001c0004t0001g0307others(7): Show | 10 | HG01123.hp1 HG01952.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.19-11083dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843896 | ||||||
| chr12:7843904
|
C | A | 165 | a0001c0002t0003g0021a0001c0002t0003g0031a0001c0002t0003g0041others(162): Show | 166 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.19-11090G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843904 | ||||||
| chr12:7843905
|
A | T | 156 | a0001c0002t0003g0031a0001c0002t0003g0041a0001c0002t0003g0053others(153): Show | 157 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.19-11091T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843905 | ||||||
| chr12:7843956
|
TTGTTG | T | 3 | a0001c0004t0001g0307a0002c0001t0002g0156a0002c0001t0002g0231 | 3 | HG01123.hp1 NA18954.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.19-11147_19-11143d others(7): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843956 | ||||||
| chr12:7843958
|
G | T | 178 | a0001c0002t0003g0021a0001c0002t0003g0031a0001c0002t0003g0041others(175): Show | 179 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(176): Show |
intron_variant | MODIFIER | c.19-11144C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843958 | ||||||
| chr12:7843961
|
GTCTTT | G | 20 | a0001c0002t0003g0021a0001c0002t0003g0031a0001c0002t0003g0196others(17): Show | 20 | HG00323.hp1 HG00673.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.19-11152_19-11148d others(7): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843961 | ||||||
| chr12:7843963
|
C | T | 3 | a0001c0004t0001g0307a0002c0001t0002g0156a0002c0001t0002g0231 | 3 | HG01123.hp1 NA18954.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.19-11149G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843963 | ||||||
| chr12:7843995
|
G | T | 161 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0256others(158): Show | 162 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(159): Show |
intron_variant | MODIFIER | c.19-11181C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7843995 | ||||||
| chr12:7844032
|
G | A | 6 | a0001c0003t0010g0098a0001c0004t0001g0331a0001c0004t0001g0332others(3): Show | 6 | HG01952.hp1 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-11218C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844032 | ||||||
| chr12:7844079
|
C | A | 3 | a0001c0002t0003g0079a0001c0002t0003g0259a0001c0004t0001g0307 | 3 | HG01123.hp1 HG01993.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.19-11265G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844079 | ||||||
| chr12:7844088
|
A | G | 2 | a0001c0002t0003g0079a0001c0002t0003g0259 | 2 | HG01993.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.19-11274T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844088 | ||||||
| chr12:7844178
|
T | C | 174 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0079others(171): Show | 175 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.19-11364A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844178 | ||||||
| chr12:7844197
|
C | T | 1 | a0002c0001t0002g0300 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.19-11383G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844197 | ||||||
| chr12:7844229
|
T | C | 1 | a0001c0005t0006g0034 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.19-11415A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844229 | ||||||
| chr12:7844294
|
C | T | 172 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0079others(169): Show | 173 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.19-11480G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844294 | ||||||
| chr12:7844442
|
T | C | 18 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(15): Show | 18 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-11628A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844442 | ||||||
| chr12:7844543
|
C | CTT | 169 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0079others(166): Show | 170 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.19-11731_19-11730d others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844543 | ||||||
| chr12:7844606
|
G | A | 154 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(151): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.19-11792C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844606 | ||||||
| chr12:7844719
|
TAA | T | 17 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(14): Show | 17 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-11907_19-11906d others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844719 | ||||||
| chr12:7844756
|
G | A | 1 | a0001c0003t0010g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.19-11942C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844756 | ||||||
| chr12:7844822
|
C | A | 1 | a0001c0006t0009g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-12008G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844822 | ||||||
| chr12:7844826
|
G | T | 18 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(15): Show | 18 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-12012C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844826 | ||||||
| chr12:7844830
|
C | T | 2 | a0001c0006t0004g0161a0002c0001t0002g0160 | 2 | HG00544.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.19-12016G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844830 | ||||||
| chr12:7844951
|
T | G | 172 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0079others(169): Show | 173 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.19-12137A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7844951 | ||||||
| chr12:7845083
|
T | G | 19 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(16): Show | 19 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.19-12269A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7845083 | ||||||
| chr12:7845219
|
G | C | 1 | a0001c0002t0003g0132 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.19-12405C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7845219 | ||||||
| chr12:7845291
|
C | A | 1 | a0001c0006t0009g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-12477G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7845291 | ||||||
| chr12:7845545
|
C | T | 1 | a0001c0003t0010g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.19-12731G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7845545 | ||||||
| chr12:7845585
|
C | T | 1 | a0001c0006t0009g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-12771G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7845585 | ||||||
| chr12:7845636
|
G | A | 1 | a0001c0008t0001g0274 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.19-12822C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7845636 | ||||||
| chr12:7845639
|
C | A | 17 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(14): Show | 17 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-12825G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7845639 | ||||||
| chr12:7845753
|
T | C | 2 | a0001c0002t0003g0292a0001c0004t0001g0197 | 2 | HG00323.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.19-12939A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7845753 | ||||||
| chr12:7845757
|
C | T | 1 | a0001c0004t0001g0326 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.19-12943G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7845757 | ||||||
| chr12:7845762
|
C | G | 1 | a0001c0003t0010g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.19-12948G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7845762 | ||||||
| chr12:7845778
|
C | CA | 319 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(316): Show | 320 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.19-12965dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7845778 | ||||||
| chr12:7846187
|
G | A | 1 | a0001c0005t0005g0229 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.19-13373C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7846187 | ||||||
| chr12:7846223
|
G | T | 1 | a0001c0007t0009g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.19-13409C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7846223 | ||||||
| chr12:7846351
|
G | A | 2 | a0001c0003t0001g0313a0001c0004t0001g0315 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.19-13537C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7846351 | ||||||
| chr12:7846404
|
TA | T | 21 | a0001c0002t0003g0079a0001c0002t0003g0196a0001c0002t0003g0206others(18): Show | 21 | HG00323.hp1 HG00673.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.19-13591delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7846404 | ||||||
| chr12:7846635
|
A | AT | 152 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0031others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.19-13822dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7846635 | ||||||
| chr12:7846635
|
AT | A | 13 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0004t0001g0195others(10): Show | 13 | HG00323.hp1 HG00673.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.19-13822delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7846635 | ||||||
| chr12:7846743
|
TGCCTCA | T | 155 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.19-13935_19-13930d others(8): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7846743 | ||||||
| chr12:7846776
|
C | T | 20 | a0001c0002t0003g0337a0001c0003t0001g0186a0001c0004t0001g0112others(17): Show | 20 | HG00642.hp1 HG01123.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.19-13962G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7846776 | ||||||
| chr12:7846826
|
G | A | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-14012C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7846826 | ||||||
| chr12:7846900
|
G | A | 2 | a0001c0003t0010g0013a0001c0003t0010g0014 | 2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.19-14086C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7846900 | ||||||
| chr12:7847134
|
C | A | 1 | a0001c0006t0009g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-14320G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7847134 | ||||||
| chr12:7847206
|
T | C | 170 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0079others(167): Show | 171 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.19-14392A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7847206 | ||||||
| chr12:7847232
|
C | A | 170 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0079others(167): Show | 171 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.19-14418G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7847232 | ||||||
| chr12:7847676
|
T | A | 1 | a0001c0004t0001g0266 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.19-14862A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7847676 | ||||||
| chr12:7847704
|
C | A | 167 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0079others(164): Show | 168 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.19-14890G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7847704 | ||||||
| chr12:7847740
|
T | G | 167 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0079others(164): Show | 168 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.19-14926A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7847740 | ||||||
| chr12:7847821
|
C | T | 1 | a0002c0001t0002g0299 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.19-15007G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7847821 | ||||||
| chr12:7847864
|
G | T | 316 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(313): Show | 317 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.19-15050C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7847864 | ||||||
| chr12:7848178
|
G | C | 319 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(316): Show | 320 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.19-15364C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848178 | ||||||
| chr12:7848316
|
G | A | 30 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.19-15502C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848316 | ||||||
| chr12:7848356
|
T | C | 1 | a0001c0005t0005g0039 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.19-15542A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848356 | ||||||
| chr12:7848381
|
TA | T | 148 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0079others(145): Show | 149 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.19-15568delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848381 | ||||||
| chr12:7848382
|
A | T | 168 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.19-15568T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848382 | ||||||
| chr12:7848399
|
T | C | 317 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(314): Show | 318 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.19-15585A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848399 | ||||||
| chr12:7848551
|
A | G | 1 | a0001c0003t0010g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.19-15737T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848551 | ||||||
| chr12:7848555
|
C | T | 1 | a0001c0006t0009g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-15741G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848555 | ||||||
| chr12:7848556
|
AT | A | 314 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(311): Show | 315 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.19-15743delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848556 | ||||||
| chr12:7848594
|
C | T | 2 | a0001c0003t0010g0098a0001c0006t0009g0081 | 2 | HG01952.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.19-15780G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848594 | ||||||
| chr12:7848603
|
T | G | 148 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0079others(145): Show | 149 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.19-15789A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848603 | ||||||
| chr12:7848666
|
C | A | 2 | a0001c0003t0010g0098a0001c0006t0009g0081 | 2 | HG01952.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.19-15852G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848666 | ||||||
| chr12:7848712
|
T | C | 2 | a0001c0003t0010g0098a0001c0006t0009g0081 | 2 | HG01952.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.19-15898A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848712 | ||||||
| chr12:7848713
|
G | A | 1 | a0001c0006t0009g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-15899C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848713 | ||||||
| chr12:7848845
|
C | T | 1 | a0001c0002t0003g0053 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.19-16031G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848845 | ||||||
| chr12:7848989
|
C | G | 346 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.19-16175G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7848989 | ||||||
| chr12:7849229
|
G | A | 7 | a0001c0004t0001g0112a0001c0005t0005g0114a0001c0006t0004g0115others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-16415C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7849229 | ||||||
| chr12:7849298
|
T | C | 1 | a0002c0001t0002g0214 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.19-16484A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7849298 | ||||||
| chr12:7849373
|
G | A | 4 | a0001c0003t0001g0298a0001c0003t0001g0303a0001c0003t0001g0308others(1): Show | 4 | HG01952.hp1 HG02735.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-16559C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7849373 | ||||||
| chr12:7849455
|
G | A | 127 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0079others(124): Show | 128 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.19-16641C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7849455 | ||||||
| chr12:7849523
|
G | T | 347 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.19-16709C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7849523 | ||||||
| chr12:7849529
|
C | T | 2 | a0001c0004t0001g0266a0001c0006t0016g0273 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.19-16715G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7849529 | ||||||
| chr12:7849586
|
A | G | 2 | a0001c0003t0010g0013a0001c0003t0010g0014 | 2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.19-16772T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7849586 | ||||||
| chr12:7849773
|
G | A | 147 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.19-16959C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7849773 | ||||||
| chr12:7849988
|
A | G | 1 | a0001c0008t0001g0274 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.19-17174T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7849988 | ||||||
| chr12:7850031
|
T | TA | 8 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0003t0001g0042others(5): Show | 8 | HG02083.hp1 HG02132.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-17218dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7850031 | ||||||
| chr12:7850031
|
T | TAA | 142 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(139): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.19-17219_19-17218d others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7850031 | ||||||
| chr12:7850045
|
A | G | 1 | a0001c0002t0003g0090 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.19-17231T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7850045 | ||||||
| chr12:7850227
|
A | T | 27 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.19-17413T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7850227 | ||||||
| chr12:7850405
|
TA | T | 3 | a0001c0004t0001g0266a0001c0006t0016g0273a0002c0001t0002g0261 | 3 | HG01167.hp1 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.19-17592delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7850405 | ||||||
| chr12:7850406
|
A | T | 314 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(311): Show | 315 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.19-17592T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7850406 | ||||||
| chr12:7850419
|
G | A | 2 | a0001c0003t0010g0098a0001c0006t0009g0081 | 2 | HG01952.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.19-17605C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7850419 | ||||||
| chr12:7850486
|
C | T | 15 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0004t0001g0195others(12): Show | 15 | HG00323.hp1 HG00673.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.19-17672G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7850486 | ||||||
| chr12:7850497
|
G | A | 1 | a0002c0009t0002g0264 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.19-17683C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7850497 | ||||||
| chr12:7850584
|
C | T | 1 | a0001c0002t0003g0111 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.19-17770G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7850584 | ||||||
| chr12:7850629
|
C | T | 3 | a0001c0005t0005g0213a0001c0005t0005g0229a0002c0001t0002g0214 | 3 | HG00597.hp2 NA18953.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.19-17815G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7850629 | ||||||
| chr12:7851128
|
C | T | 1 | a0001c0003t0010g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.19-18314G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7851128 | ||||||
| chr12:7851162
|
G | A | 145 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(142): Show | 145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.19-18348C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7851162 | ||||||
| chr12:7851763
|
T | C | 1 | a0001c0003t0014g0139 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.18+18100A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7851763 | ||||||
| chr12:7851945
|
A | T | 1 | a0001c0003t0001g0117 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.18+17918T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7851945 | ||||||
| chr12:7851958
|
C | T | 1 | a0001c0004t0001g0106 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.18+17905G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7851958 | ||||||
| chr12:7852188
|
C | T | 1 | a0001c0003t0010g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.18+17675G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7852188 | ||||||
| chr12:7852274
|
G | A | 2 | a0001c0003t0010g0013a0001c0003t0010g0014 | 2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.18+17589C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7852274 | ||||||
| chr12:7852369
|
A | T | 147 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.18+17494T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7852369 | ||||||
| chr12:7853028
|
G | A | 1 | a0002c0001t0002g0001 | 2 | HG01081.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.18+16835C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7853028 | ||||||
| chr12:7853369
|
G | A | 2 | a0001c0004t0001g0266a0001c0006t0016g0273 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.18+16494C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7853369 | ||||||
| chr12:7853379
|
C | T | 2 | a0001c0002t0003g0090a0001c0007t0004g0146 | 2 | HG00140.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.18+16484G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7853379 | ||||||
| chr12:7853429
|
C | CA | 216 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(213): Show | 217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.18+16433dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7853429 | ||||||
| chr12:7853429
|
C | CAA | 26 | a0001c0002t0003g0044a0001c0002t0003g0079a0001c0002t0003g0259others(23): Show | 26 | HG00423.hp1 HG01175.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.18+16432_18+16433d others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7853429 | ||||||
| chr12:7853429
|
C | CAAA | 9 | a0001c0003t0001g0077a0001c0003t0001g0187a0001c0003t0001g0188others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+16431_18+16433d others(5): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7853429 | ||||||
| chr12:7853429
|
CAAAAAA | C | 10 | a0001c0003t0001g0192a0001c0003t0001g0316a0001c0003t0001g0317others(7): Show | 10 | HG01891.hp1 HG01952.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.18+16428_18+16433d others(8): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7853429 | ||||||
| chr12:7853429
|
CAAAAAAA | C | 7 | a0001c0002t0003g0148a0001c0008t0001g0099a0002c0001t0002g0101others(4): Show | 7 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+16427_18+16433d others(9): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7853429 | ||||||
| chr12:7853470
|
C | T | 1 | a0001c0002t0003g0259 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.18+16393G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7853470 | ||||||
| chr12:7853569
|
C | A | 27 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.18+16294G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7853569 | ||||||
| chr12:7853744
|
A | C | 1 | a0005c0015t0008g0341 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.18+16119T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7853744 | ||||||
| chr12:7853915
|
T | C | 30 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.18+15948A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7853915 | ||||||
| chr12:7854031
|
A | C | 2 | a0001c0003t0010g0098a0001c0006t0009g0081 | 2 | HG01952.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.18+15832T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7854031 | ||||||
| chr12:7854064
|
A | G | 1 | a0001c0002t0003g0142 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.18+15799T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7854064 | ||||||
| chr12:7854109
|
T | C | 1 | a0001c0003t0010g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.18+15754A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7854109 | ||||||
| chr12:7854396
|
A | G | 1 | a0001c0003t0010g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.18+15467T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7854396 | ||||||
| chr12:7854497
|
T | C | 1 | a0001c0003t0010g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.18+15366A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7854497 | ||||||
| chr12:7854671
|
C | T | 1 | a0002c0001t0002g0104 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.18+15192G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7854671 | ||||||
| chr12:7854679
|
G | A | 6 | a0001c0004t0001g0096a0001c0004t0001g0097a0001c0004t0001g0254others(3): Show | 6 | HG00639.hp1 HG01257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+15184C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7854679 | ||||||
| chr12:7854691
|
A | G | 1 | a0001c0004t0001g0109 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.18+15172T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7854691 | ||||||
| chr12:7854874
|
G | A | 24 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0256others(21): Show | 25 | HG01071.hp1 HG01074.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.18+14989C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7854874 | ||||||
| chr12:7855001
|
G | C | 145 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(142): Show | 145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.18+14862C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855001 | ||||||
| chr12:7855011
|
T | C | 4 | a0001c0002t0003g0144a0001c0002t0003g0176a0001c0004t0001g0109others(1): Show | 4 | HG00280.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+14852A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855011 | ||||||
| chr12:7855115
|
G | A | 1 | a0001c0002t0003g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.18+14748C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855115 | ||||||
| chr12:7855163
|
T | G | 1 | a0001c0003t0010g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.18+14700A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855163 | ||||||
| chr12:7855286
|
G | C | 8 | a0001c0003t0010g0098a0001c0004t0001g0096a0001c0004t0001g0097others(5): Show | 8 | HG00639.hp1 HG01257.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+14577C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855286 | ||||||
| chr12:7855322
|
G | C | 2 | a0001c0007t0009g0078a0001c0007t0009g0291 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.18+14541C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855322 | ||||||
| chr12:7855432
|
C | A | 342 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(339): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.18+14431G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855432 | ||||||
| chr12:7855536
|
C | A | 32 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(29): Show | 32 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.18+14327G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855536 | ||||||
| chr12:7855583
|
C | T | 86 | a0001c0002t0003g0041a0001c0002t0003g0044a0001c0002t0003g0054others(83): Show | 87 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.18+14280G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855583 | ||||||
| chr12:7855627
|
C | CT | 103 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0079others(100): Show | 104 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.18+14235dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855627 | ||||||
| chr12:7855699
|
A | ACGGTTTC others(15): Show |
48 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(45): Show | 48 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.18+14163_18+14164i others(24): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855699 | ||||||
| chr12:7855703
|
C | CTTCAGCT others(15): Show |
1 | a0001c0002t0003g0111 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.18+14159_18+14160i others(24): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855703 | ||||||
| chr12:7855703
|
C | T | 48 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(45): Show | 48 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.18+14160G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855703 | ||||||
| chr12:7855720
|
C | A | 2 | a0001c0003t0001g0135a0001c0003t0001g0136 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.18+14143G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855720 | ||||||
| chr12:7855797
|
C | T | 1 | a0001c0002t0003g0148 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.18+14066G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855797 | ||||||
| chr12:7855887
|
A | C | 4 | a0001c0003t0001g0272a0002c0001t0002g0270a0002c0001t0002g0271others(1): Show | 4 | HG01884.hp1 HG02486.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+13976T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7855887 | ||||||
| chr12:7856187
|
G | A | 3 | a0001c0004t0001g0011a0001c0004t0001g0339a0002c0001t0002g0012 | 3 | HG01884.hp2 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.18+13676C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7856187 | ||||||
| chr12:7856278
|
G | A | 1 | a0002c0001t0002g0101 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.18+13585C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7856278 | ||||||
| chr12:7856455
|
A | G | 1 | a0001c0004t0001g0266 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+13408T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7856455 | ||||||
| chr12:7856456
|
G | A | 1 | a0001c0004t0001g0266 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+13407C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7856456 | ||||||
| chr12:7856516
|
G | A | 83 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.18+13347C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7856516 | ||||||
| chr12:7856557
|
C | T | 16 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0256others(13): Show | 17 | HG01071.hp1 HG01074.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.18+13306G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7856557 | ||||||
| chr12:7856744
|
G | A | 1 | a0002c0011t0008g0289 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.18+13119C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7856744 | ||||||
| chr12:7856811
|
C | G | 5 | a0001c0002t0003g0337a0001c0005t0005g0334a0001c0005t0005g0335others(2): Show | 5 | HG00642.hp1 HG01123.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+13052G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7856811 | ||||||
| chr12:7856839
|
A | AT | 82 | a0001c0002t0003g0041a0001c0002t0003g0054a0001c0002t0003g0107others(79): Show | 82 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+13023dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7856839 | ||||||
| chr12:7856839
|
AT | A | 62 | a0001c0002t0003g0055a0001c0002t0003g0196a0001c0002t0003g0206others(59): Show | 62 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.18+13023delA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7856839 | ||||||
| chr12:7856923
|
A | G | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+12940T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7856923 | ||||||
| chr12:7856979
|
C | T | 52 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.18+12884G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7856979 | ||||||
| chr12:7857018
|
A | G | 1 | a0001c0003t0001g0024 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.18+12845T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7857018 | ||||||
| chr12:7857034
|
G | A | 30 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(27): Show | 30 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.18+12829C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7857034 | ||||||
| chr12:7857352
|
G | T | 1 | a0001c0004t0001g0248 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.18+12511C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7857352 | ||||||
| chr12:7857510
|
G | C | 52 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.18+12353C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7857510 | ||||||
| chr12:7857532
|
G | A | 3 | a0001c0003t0001g0028a0001c0005t0006g0006a0001c0005t0015g0029 | 3 | NA18941.hp2 NA19002.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.18+12331C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7857532 | ||||||
| chr12:7857639
|
C | A | 1 | a0001c0005t0005g0336 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.18+12224G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7857639 | ||||||
| chr12:7857776
|
T | C | 1 | a0001c0005t0005g0205 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.18+12087A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7857776 | ||||||
| chr12:7858044
|
T | A | 53 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(50): Show | 53 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.18+11819A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858044 | ||||||
| chr12:7858082
|
G | A | 1 | a0001c0003t0001g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.18+11781C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858082 | ||||||
| chr12:7858119
|
C | T | 2 | a0001c0004t0001g0285a0001c0006t0009g0284 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.18+11744G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858119 | ||||||
| chr12:7858190
|
T | C | 1 | a0002c0001t0002g0321 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.18+11673A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858190 | ||||||
| chr12:7858335
|
G | C | 1 | a0001c0002t0003g0142 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.18+11528C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858335 | ||||||
| chr12:7858353
|
T | C | 1 | a0001c0004t0001g0106 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.18+11510A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858353 | ||||||
| chr12:7858365
|
G | A | 1 | a0001c0004t0001g0306 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.18+11498C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858365 | ||||||
| chr12:7858388
|
T | A | 1 | a0001c0004t0001g0248 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.18+11475A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858388 | ||||||
| chr12:7858530
|
G | A | 8 | a0001c0004t0001g0236a0001c0004t0001g0237a0001c0004t0001g0248others(5): Show | 8 | HG00738.hp1 HG02486.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+11333C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858530 | ||||||
| chr12:7858581
|
C | A | 23 | a0001c0002t0003g0337a0001c0003t0001g0316a0001c0003t0001g0317others(20): Show | 23 | HG00642.hp1 HG01123.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.18+11282G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858581 | ||||||
| chr12:7858584
|
C | A | 9 | a0001c0008t0001g0238a0001c0008t0001g0239a0001c0008t0001g0240others(6): Show | 9 | HG00597.hp1 HG02083.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+11279G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858584 | ||||||
| chr12:7858658
|
C | T | 1 | a0001c0005t0005g0340 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.18+11205G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858658 | ||||||
| chr12:7858681
|
T | G | 6 | a0001c0003t0001g0313a0001c0004t0001g0315a0001c0006t0004g0286others(3): Show | 6 | HG02559.hp2 HG02965.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+11182A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858681 | ||||||
| chr12:7858728
|
A | G | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+11135T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858728 | ||||||
| chr12:7858871
|
A | G | 1 | a0001c0005t0005g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.18+10992T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7858871 | ||||||
| chr12:7859140
|
G | A | 1 | a0001c0004t0001g0248 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.18+10723C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859140 | ||||||
| chr12:7859362
|
C | G | 23 | a0001c0002t0003g0337a0001c0003t0001g0316a0001c0003t0001g0317others(20): Show | 23 | HG00642.hp1 HG01123.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.18+10501G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859362 | ||||||
| chr12:7859705
|
C | T | 1 | a0001c0003t0001g0145 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.18+10158G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859705 | ||||||
| chr12:7859718
|
C | A | 20 | a0001c0002t0003g0089a0001c0003t0001g0083a0001c0003t0014g0139others(17): Show | 20 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.18+10145G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859718 | ||||||
| chr12:7859800
|
A | G | 1 | a0001c0004t0001g0266 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+10063T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859800 | ||||||
| chr12:7859858
|
CCTCTAAC others(4): Show |
C | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+9994_18+10004de others(12): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859858 | ||||||
| chr12:7859860
|
T | G | 56 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(53): Show | 56 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.18+10003A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859860 | ||||||
| chr12:7859871
|
A | C | 52 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.18+9992T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859871 | ||||||
| chr12:7859988
|
C | A | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+9875G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859988 | ||||||
| chr12:7859989
|
C | G | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+9874G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859989 | ||||||
| chr12:7859992
|
A | G | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+9871T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859992 | ||||||
| chr12:7859995
|
G | A | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+9868C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859995 | ||||||
| chr12:7859996
|
C | G | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+9867G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7859996 | ||||||
| chr12:7860005
|
C | T | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+9858G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7860005 | ||||||
| chr12:7860009
|
A | G | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+9854T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7860009 | ||||||
| chr12:7860064
|
G | C | 1 | a0002c0010t0002g0243 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.18+9799C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7860064 | ||||||
| chr12:7860389
|
C | G | 73 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0256others(70): Show | 74 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.18+9474G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7860389 | ||||||
| chr12:7860483
|
T | C | 53 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(50): Show | 53 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.18+9380A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7860483 | ||||||
| chr12:7860665
|
T | C | 1 | a0001c0016t0008g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18+9198A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7860665 | ||||||
| chr12:7860712
|
C | T | 1 | a0001c0004t0001g0106 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.18+9151G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7860712 | ||||||
| chr12:7860793
|
C | CT | 135 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0090others(132): Show | 136 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.18+9069dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7860793 | ||||||
| chr12:7860861
|
C | T | 53 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(50): Show | 53 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.18+9002G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7860861 | ||||||
| chr12:7860918
|
G | A | 1 | a0002c0001t0002g0030 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.18+8945C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7860918 | ||||||
| chr12:7860921
|
T | A | 4 | a0001c0004t0001g0171a0001c0005t0005g0140a0001c0005t0005g0172others(1): Show | 4 | HG01074.hp1 HG02738.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+8942A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7860921 | ||||||
| chr12:7860974
|
T | C | 73 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0256others(70): Show | 74 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.18+8889A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7860974 | ||||||
| chr12:7861083
|
C | T | 160 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(157): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.18+8780G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7861083 | ||||||
| chr12:7861445
|
A | G | 293 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.18+8418T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7861445 | ||||||
| chr12:7861559
|
G | A | 3 | a0001c0004t0001g0343a0001c0005t0005g0342a0005c0015t0008g0341 | 3 | HG02280.hp2 HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.18+8304C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7861559 | ||||||
| chr12:7861625
|
C | G | 1 | a0001c0004t0001g0185 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.18+8238G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7861625 | ||||||
| chr12:7861634
|
T | C | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+8229A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7861634 | ||||||
| chr12:7861664
|
T | C | 4 | a0001c0004t0001g0331a0001c0004t0001g0332a0001c0004t0001g0333others(1): Show | 4 | HG02922.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+8199A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7861664 | ||||||
| chr12:7861771
|
G | A | 23 | a0001c0002t0003g0337a0001c0003t0001g0316a0001c0003t0001g0317others(20): Show | 23 | HG00642.hp1 HG01123.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.18+8092C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7861771 | ||||||
| chr12:7861816
|
G | C | 1 | a0001c0002t0003g0206 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.18+8047C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7861816 | ||||||
| chr12:7861961
|
C | CA | 266 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.18+7901dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7861961 | ||||||
| chr12:7861961
|
C | CAA | 22 | a0001c0002t0003g0066a0001c0002t0003g0076a0001c0003t0001g0244others(19): Show | 22 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.18+7900_18+7901dup others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7861961 | ||||||
| chr12:7862019
|
A | G | 1 | a0001c0003t0001g0095 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.18+7844T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862019 | ||||||
| chr12:7862241
|
G | T | 2 | a0001c0004t0001g0296a0001c0004t0001g0297 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.18+7622C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862241 | ||||||
| chr12:7862264
|
C | CA | 115 | a0001c0002t0003g0092a0001c0002t0003g0093a0001c0002t0003g0094others(112): Show | 115 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.18+7598dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862264 | ||||||
| chr12:7862264
|
C | CAA | 24 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0256others(21): Show | 25 | HG01071.hp1 HG01074.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.18+7597_18+7598dup others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862264 | ||||||
| chr12:7862264
|
CA | C | 10 | a0001c0002t0003g0105a0001c0002t0003g0144a0001c0004t0001g0296others(7): Show | 10 | HG01168.hp2 HG01943.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.18+7598delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862264 | ||||||
| chr12:7862264
|
CAAA | C | 7 | a0001c0003t0001g0018a0001c0003t0001g0056a0001c0003t0001g0058others(4): Show | 7 | NA18941.hp1 NA18945.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+7596_18+7598del others(3): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862264 | ||||||
| chr12:7862411
|
C | T | 1 | a0001c0004t0001g0195 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.18+7452G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862411 | ||||||
| chr12:7862422
|
C | T | 1 | a0001c0002t0003g0087 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.18+7441G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862422 | ||||||
| chr12:7862438
|
A | G | 5 | a0001c0002t0003g0091a0001c0002t0003g0092a0001c0002t0003g0093others(2): Show | 5 | HG00099.hp1 HG00642.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+7425T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862438 | ||||||
| chr12:7862495
|
G | A | 3 | a0001c0004t0001g0011a0001c0004t0001g0339a0002c0001t0002g0012 | 3 | HG01884.hp2 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.18+7368C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862495 | ||||||
| chr12:7862504
|
C | A | 73 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0256others(70): Show | 74 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.18+7359G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862504 | ||||||
| chr12:7862617
|
C | T | 2 | a0001c0002t0003g0090a0001c0007t0004g0146 | 2 | HG00140.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.18+7246G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862617 | ||||||
| chr12:7862876
|
T | G | 34 | a0001c0002t0003g0090a0001c0002t0003g0091a0001c0002t0003g0092others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.18+6987A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862876 | ||||||
| chr12:7862924
|
C | A | 292 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(289): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.18+6939G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862924 | ||||||
| chr12:7862924
|
C | G | 54 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0258others(51): Show | 54 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.18+6939G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7862924 | ||||||
| chr12:7863186
|
C | A | 1 | a0002c0011t0008g0003 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.18+6677G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863186 | ||||||
| chr12:7863186
|
C | G | 156 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.18+6677G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863186 | ||||||
| chr12:7863187
|
G | A | 346 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.18+6676C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863187 | ||||||
| chr12:7863189
|
A | G | 346 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.18+6674T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863189 | ||||||
| chr12:7863302
|
C | A | 2 | a0001c0004t0001g0285a0001c0006t0009g0284 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.18+6561G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863302 | ||||||
| chr12:7863467
|
A | C | 1 | a0002c0001t0002g0002 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.18+6396T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863467 | ||||||
| chr12:7863651
|
G | A | 348 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.18+6212C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863651 | ||||||
| chr12:7863670
|
C | G | 298 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.18+6193G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863670 | ||||||
| chr12:7863800
|
A | G | 1 | a0001c0004t0001g0266 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+6063T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863800 | ||||||
| chr12:7863815
|
CTTTTTTT others(3): Show |
C | 49 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(46): Show | 49 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.18+6038_18+6047del others(10): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863815 | ||||||
| chr12:7863823
|
CTT | C | 295 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(292): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.18+6038_18+6039del others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863823 | ||||||
| chr12:7863927
|
C | T | 1 | a0001c0004t0001g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.18+5936G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863927 | ||||||
| chr12:7863928
|
G | A | 33 | a0001c0002t0003g0292a0001c0002t0003g0293a0001c0002t0003g0302others(30): Show | 33 | HG00280.hp1 HG00735.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.18+5935C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863928 | ||||||
| chr12:7863929
|
C | T | 49 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(46): Show | 49 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.18+5934G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7863929 | ||||||
| chr12:7864023
|
A | G | 157 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.18+5840T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864023 | ||||||
| chr12:7864024
|
G | C | 157 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.18+5839C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864024 | ||||||
| chr12:7864230
|
C | T | 1 | a0001c0006t0004g0324 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.18+5633G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864230 | ||||||
| chr12:7864238
|
C | T | 1 | a0001c0004t0001g0266 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+5625G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864238 | ||||||
| chr12:7864245
|
A | G | 1 | a0002c0001t0002g0155 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.18+5618T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864245 | ||||||
| chr12:7864326
|
A | G | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+5537T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864326 | ||||||
| chr12:7864329
|
G | A | 48 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(45): Show | 48 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.18+5534C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864329 | ||||||
| chr12:7864404
|
T | C | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5459A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864404 | ||||||
| chr12:7864408
|
A | C | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5455T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864408 | ||||||
| chr12:7864418
|
A | G | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5445T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864418 | ||||||
| chr12:7864420
|
C | T | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5443G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864420 | ||||||
| chr12:7864424
|
C | G | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5439G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864424 | ||||||
| chr12:7864425
|
G | C | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5438C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864425 | ||||||
| chr12:7864426
|
C | G | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5437G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864426 | ||||||
| chr12:7864427
|
C | A | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5436G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864427 | ||||||
| chr12:7864430
|
C | T | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5433G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864430 | ||||||
| chr12:7864438
|
A | C | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5425T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864438 | ||||||
| chr12:7864441
|
C | G | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5422G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864441 | ||||||
| chr12:7864450
|
T | A | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5413A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864450 | ||||||
| chr12:7864457
|
G | T | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5406C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864457 | ||||||
| chr12:7864463
|
C | A | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5400G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864463 | ||||||
| chr12:7864465
|
A | G | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5398T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864465 | ||||||
| chr12:7864469
|
G | T | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5394C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864469 | ||||||
| chr12:7864494
|
A | T | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5369T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864494 | ||||||
| chr12:7864495
|
T | G | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5368A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864495 | ||||||
| chr12:7864497
|
C | G | 1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5366G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864497 | ||||||
| chr12:7864498
|
C | CCTGGCCT others(3): Show |
1 | a0001c0008t0001g0023 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+5364_18+5365ins others(10): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864498 | ||||||
| chr12:7864560
|
G | A | 1 | a0002c0001t0002g0037 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.18+5303C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864560 | ||||||
| chr12:7864590
|
G | A | 2 | a0002c0001t0002g0002a0002c0011t0008g0003 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.18+5273C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864590 | ||||||
| chr12:7864607
|
G | A | 1 | a0001c0004t0001g0248 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.18+5256C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864607 | ||||||
| chr12:7864763
|
G | A | 1 | a0002c0001t0002g0325 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.18+5100C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864763 | ||||||
| chr12:7864807
|
G | A | 1 | a0002c0001t0002g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.18+5056C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864807 | ||||||
| chr12:7864831
|
A | G | 156 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.18+5032T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864831 | ||||||
| chr12:7864862
|
C | T | 51 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.18+5001G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864862 | ||||||
| chr12:7864882
|
T | C | 152 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0196others(149): Show | 153 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.18+4981A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864882 | ||||||
| chr12:7864899
|
C | G | 73 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0256others(70): Show | 74 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.18+4964G>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7864899 | ||||||
| chr12:7865136
|
C | T | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+4727G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865136 | ||||||
| chr12:7865160
|
G | A | 1 | a0001c0004t0001g0248 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.18+4703C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865160 | ||||||
| chr12:7865222
|
A | G | 15 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0004t0001g0195others(12): Show | 15 | HG00323.hp1 HG00673.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.18+4641T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865222 | ||||||
| chr12:7865245
|
T | C | 59 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0002t0003g0292others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.18+4618A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865245 | ||||||
| chr12:7865257
|
G | C | 193 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.18+4606C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865257 | ||||||
| chr12:7865286
|
C | T | 173 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.18+4577G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865286 | ||||||
| chr12:7865308
|
T | C | 4 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0006t0004g0073others(1): Show | 4 | HG01106.hp1 HG01109.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+4555A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865308 | ||||||
| chr12:7865353
|
T | C | 20 | a0001c0002t0003g0041a0001c0002t0003g0044a0001c0002t0003g0054others(17): Show | 20 | HG00408.hp2 HG00423.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.18+4510A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865353 | ||||||
| chr12:7865358
|
G | A | 20 | a0001c0002t0003g0041a0001c0002t0003g0044a0001c0002t0003g0054others(17): Show | 20 | HG00408.hp2 HG00423.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.18+4505C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865358 | ||||||
| chr12:7865379
|
C | T | 1 | a0002c0001t0002g0032 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.18+4484G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865379 | ||||||
| chr12:7865548
|
T | A | 1 | a0001c0004t0001g0307 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.18+4315A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865548 | ||||||
| chr12:7865599
|
C | T | 2 | a0001c0002t0003g0090a0001c0007t0004g0146 | 2 | HG00140.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.18+4264G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865599 | ||||||
| chr12:7865942
|
C | A | 157 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.18+3921G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7865942 | ||||||
| chr12:7866224
|
C | CA | 57 | a0001c0002t0003g0053a0001c0002t0003g0054a0001c0002t0003g0292others(54): Show | 57 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.18+3638dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866224 | ||||||
| chr12:7866224
|
C | CAA | 70 | a0001c0002t0003g0079a0001c0002t0003g0257a0001c0002t0003g0258others(67): Show | 71 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.18+3637_18+3638dup others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866224 | ||||||
| chr12:7866239
|
A | G | 3 | a0001c0007t0004g0275a0001c0008t0001g0274a0002c0001t0002g0276 | 3 | HG03704.hp2 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.18+3624T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866239 | ||||||
| chr12:7866269
|
C | T | 1 | a0001c0006t0004g0207 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.18+3594G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866269 | ||||||
| chr12:7866271
|
G | T | 1 | a0001c0006t0004g0207 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.18+3592C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866271 | ||||||
| chr12:7866374
|
A | T | 100 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0196others(97): Show | 101 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.18+3489T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866374 | ||||||
| chr12:7866406
|
G | A | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+3457C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866406 | ||||||
| chr12:7866525
|
C | T | 1 | a0001c0004t0001g0185 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.18+3338G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866525 | ||||||
| chr12:7866599
|
C | T | 1 | a0001c0002t0003g0031 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.18+3264G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866599 | ||||||
| chr12:7866703
|
G | A | 1 | a0001c0004t0001g0266 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+3160C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866703 | ||||||
| chr12:7866715
|
G | A | 1 | a0002c0001t0002g0295 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.18+3148C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866715 | ||||||
| chr12:7866723
|
A | G | 1 | a0001c0002t0003g0277 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.18+3140T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866723 | ||||||
| chr12:7866842
|
T | C | 347 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.18+3021A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866842 | ||||||
| chr12:7866944
|
G | GT | 12 | a0001c0002t0003g0054a0001c0002t0003g0075a0001c0002t0003g0196others(9): Show | 12 | HG01106.hp1 HG01891.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.18+2918dupA | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866944 | ||||||
| chr12:7866980
|
C | T | 1 | a0001c0008t0001g0274 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.18+2883G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7866980 | ||||||
| chr12:7867051
|
G | A | 348 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.18+2812C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867051 | ||||||
| chr12:7867054
|
T | C | 348 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.18+2809A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867054 | ||||||
| chr12:7867055
|
G | A | 348 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.18+2808C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867055 | ||||||
| chr12:7867280
|
CA | C | 46 | a0001c0002t0003g0031a0001c0002t0003g0041a0001c0002t0003g0044others(43): Show | 46 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.18+2582delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867280 | ||||||
| chr12:7867280
|
CAA | C | 28 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(25): Show | 28 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.18+2581_18+2582del others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867280 | ||||||
| chr12:7867280
|
CAAAA | C | 97 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0196others(94): Show | 98 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.18+2579_18+2582del others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867280 | ||||||
| chr12:7867295
|
A | C | 100 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0196others(97): Show | 101 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.18+2568T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867295 | ||||||
| chr12:7867297
|
AAAAC | A | 45 | a0001c0002t0003g0292a0001c0002t0003g0293a0001c0002t0003g0302others(42): Show | 45 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.18+2562_18+2565del others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867297 | ||||||
| chr12:7867298
|
A | C | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+2565T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867298 | ||||||
| chr12:7867298
|
AAAC | A | 12 | a0001c0002t0003g0089a0001c0003t0001g0328a0001c0003t0001g0329others(9): Show | 12 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.18+2562_18+2564del others(3): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867298 | ||||||
| chr12:7867299
|
AAC | A | 70 | a0001c0002t0003g0080a0001c0002t0003g0082a0001c0002t0003g0087others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.18+2562_18+2563del others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867299 | ||||||
| chr12:7867300
|
AC | A | 34 | a0001c0002t0003g0147a0001c0002t0003g0148a0001c0002t0003g0159others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.18+2562delG | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867300 | ||||||
| chr12:7867301
|
C | A | 3 | a0001c0005t0006g0178a0002c0001t0002g0177a0002c0001t0002g0179 | 3 | HG03017.hp2 NA18977.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.18+2562G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867301 | ||||||
| chr12:7867306
|
A | C | 58 | a0001c0002t0003g0292a0001c0002t0003g0293a0001c0002t0003g0302others(55): Show | 58 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.18+2557T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867306 | ||||||
| chr12:7867309
|
AC | A | 100 | a0001c0002t0003g0079a0001c0002t0003g0085a0001c0002t0003g0196others(97): Show | 101 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.18+2553delG | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867309 | ||||||
| chr12:7867386
|
G | A | 20 | a0001c0002t0003g0066a0001c0002t0003g0075a0001c0002t0003g0076others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.18+2477C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867386 | ||||||
| chr12:7867447
|
C | T | 1 | a0001c0002t0003g0087 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.18+2416G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867447 | ||||||
| chr12:7867498
|
A | G | 189 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.18+2365T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867498 | ||||||
| chr12:7867578
|
G | A | 28 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0003t0001g0077others(25): Show | 28 | HG00323.hp1 HG00673.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.18+2285C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867578 | ||||||
| chr12:7867789
|
G | A | 2 | a0002c0001t0002g0310a0002c0001t0002g0311 | 2 | NA18944.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.18+2074C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867789 | ||||||
| chr12:7867844
|
C | CA | 26 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0003t0001g0077others(23): Show | 26 | HG00323.hp1 HG00673.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+2018dupT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867844 | ||||||
| chr12:7867844
|
CA | C | 171 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.18+2018delT | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867844 | ||||||
| chr12:7867844
|
CAA | C | 14 | a0001c0003t0001g0018a0001c0003t0010g0013a0001c0003t0010g0014others(11): Show | 14 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+2017_18+2018del others(2): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867844 | ||||||
| chr12:7867887
|
A | G | 56 | a0001c0002t0003g0292a0001c0002t0003g0293a0001c0002t0003g0302others(53): Show | 56 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.18+1976T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867887 | ||||||
| chr12:7867899
|
C | T | 51 | a0001c0002t0003g0292a0001c0002t0003g0293a0001c0002t0003g0302others(48): Show | 51 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.18+1964G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867899 | ||||||
| chr12:7867900
|
G | C | 107 | a0001c0002t0003g0080a0001c0002t0003g0082a0001c0002t0003g0087others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.18+1963C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867900 | ||||||
| chr12:7867957
|
TTAA | T | 80 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(77): Show | 80 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.18+1903_18+1905del others(3): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7867957 | ||||||
| chr12:7868152
|
C | T | 2 | a0001c0004t0001g0285a0001c0006t0009g0284 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.18+1711G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7868152 | ||||||
| chr12:7868157
|
A | G | 1 | a0002c0001t0002g0194 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.18+1706T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7868157 | ||||||
| chr12:7868338
|
G | A | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+1525C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7868338 | ||||||
| chr12:7868413
|
C | T | 348 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.18+1450G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7868413 | ||||||
| chr12:7868595
|
T | C | 31 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0003t0001g0077others(28): Show | 31 | HG00323.hp1 HG00673.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.18+1268A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7868595 | ||||||
| chr12:7868630
|
G | A | 348 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.18+1233C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7868630 | ||||||
| chr12:7868704
|
G | C | 5 | a0001c0002t0003g0337a0001c0005t0005g0334a0001c0005t0005g0335others(2): Show | 5 | HG00642.hp1 HG01123.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+1159C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7868704 | ||||||
| chr12:7868739
|
C | T | 1 | a0001c0004t0001g0266 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+1124G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7868739 | ||||||
| chr12:7868755
|
C | T | 1 | a0001c0008t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.18+1108G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7868755 | ||||||
| chr12:7868756
|
C | T | 99 | a0001c0002t0003g0079a0001c0002t0003g0196a0001c0002t0003g0206others(96): Show | 100 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.18+1107G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7868756 | ||||||
| chr12:7868908
|
G | T | 191 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.18+955C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7868908 | ||||||
| chr12:7868962
|
T | G | 11 | a0001c0003t0001g0077a0001c0003t0001g0187a0001c0003t0001g0188others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.18+901A>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7868962 | ||||||
| chr12:7869066
|
C | A | 1 | a0001c0007t0009g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.18+797G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869066 | ||||||
| chr12:7869066
|
C | T | 1 | a0001c0005t0006g0006 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.18+797G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869066 | ||||||
| chr12:7869076
|
G | A | 80 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(77): Show | 80 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.18+787C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869076 | ||||||
| chr12:7869108
|
CG | C | 4 | a0001c0002t0003g0337a0001c0005t0005g0335a0001c0005t0005g0336others(1): Show | 4 | HG00642.hp1 HG01123.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+754delC | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869108 | ||||||
| chr12:7869113
|
T | C | 57 | a0001c0002t0003g0292a0001c0002t0003g0293a0001c0002t0003g0302others(54): Show | 57 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.18+750A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869113 | ||||||
| chr12:7869156
|
A | AAAAAC | 28 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0003t0001g0077others(25): Show | 28 | HG00323.hp1 HG00673.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.18+706_18+707insGT others(3): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869156 | ||||||
| chr12:7869301
|
C | T | 3 | a0001c0004t0001g0294a0001c0004t0001g0312a0002c0001t0002g0295 | 3 | HG01099.hp2 HG01192.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.18+562G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869301 | ||||||
| chr12:7869323
|
G | A | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+540C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869323 | ||||||
| chr12:7869336
|
C | A | 77 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(74): Show | 77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.18+527G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869336 | ||||||
| chr12:7869548
|
C | T | 1 | a0001c0002t0003g0293 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.18+315G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869548 | ||||||
| chr12:7869575
|
C | T | 1 | a0001c0002t0003g0292 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.18+288G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869575 | ||||||
| chr12:7869607
|
T | C | 1 | a0001c0005t0005g0340 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.18+256A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869607 | ||||||
| chr12:7869670
|
A | C | 3 | a0001c0003t0001g0272a0002c0001t0002g0270a0002c0001t0002g0271 | 3 | HG02486.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.18+193T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869670 | ||||||
| chr12:7869733
|
T | C | 13 | a0001c0002t0003g0196a0001c0002t0003g0206a0001c0004t0001g0195others(10): Show | 13 | HG00323.hp1 HG00673.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.18+130A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869733 | ||||||
| chr12:7869819
|
T | C | 1 | a0001c0004t0001g0312 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.18+44A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 2/10 | chr12 | 7869819 | ||||||
| chr12:7869983
|
A | C | 1 | a0001c0005t0006g0005 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-57-46T>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7869983 | ||||||
| chr12:7870186
|
C | T | 1 | a0001c0003t0001g0083 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-57-249G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870186 | ||||||
| chr12:7870297
|
T | A | 121 | a0001c0002t0003g0079a0001c0002t0003g0080a0001c0002t0003g0082others(118): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.-57-360A>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870297 | ||||||
| chr12:7870313
|
T | C | 1 | a0002c0001t0002g0180 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-57-376A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870313 | ||||||
| chr12:7870413
|
G | A | 2 | a0001c0004t0001g0267a0001c0004t0001g0268 | 2 | HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-57-476C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870413 | ||||||
| chr12:7870551
|
T | C | 4 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0006t0004g0073others(1): Show | 4 | HG01106.hp1 HG01109.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-614A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870551 | ||||||
| chr12:7870580
|
C | T | 200 | a0001c0002t0003g0079a0001c0002t0003g0080a0001c0002t0003g0082others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-57-643G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870580 | ||||||
| chr12:7870619
|
A | G | 205 | a0001c0002t0003g0079a0001c0002t0003g0080a0001c0002t0003g0082others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.-57-682T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870619 | ||||||
| chr12:7870680
|
G | T | 51 | a0001c0002t0003g0082a0001c0002t0003g0196a0001c0002t0003g0206others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.-57-743C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870680 | ||||||
| chr12:7870763
|
CAAAT | C | 4 | a0001c0003t0001g0272a0001c0006t0016g0273a0002c0001t0002g0270others(1): Show | 4 | HG02486.hp2 HG02723.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-830_-57-827del others(4): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870763 | ||||||
| chr12:7870873
|
GC | G | 3 | a0001c0007t0004g0275a0001c0008t0001g0274a0002c0001t0002g0276 | 3 | HG03704.hp2 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-57-937delG | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870873 | ||||||
| chr12:7870878
|
GACC | G | 209 | a0001c0002t0003g0079a0001c0002t0003g0080a0001c0002t0003g0082others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-57-944_-57-942del others(3): Show |
SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870878 | ||||||
| chr12:7870904
|
A | G | 290 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.-57-967T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870904 | ||||||
| chr12:7870934
|
C | T | 105 | a0001c0002t0003g0080a0001c0002t0003g0082a0001c0002t0003g0085others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.-57-997G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7870934 | ||||||
| chr12:7871002
|
A | T | 290 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.-57-1065T>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871002 | ||||||
| chr12:7871084
|
G | T | 57 | a0001c0002t0003g0292a0001c0002t0003g0293a0001c0002t0003g0302others(54): Show | 57 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.-57-1147C>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871084 | ||||||
| chr12:7871187
|
A | G | 1 | a0001c0002t0003g0080 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-57-1250T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871187 | ||||||
| chr12:7871322
|
T | C | 79 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(76): Show | 79 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.-57-1385A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871322 | ||||||
| chr12:7871347
|
T | C | 147 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(144): Show | 147 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.-57-1410A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871347 | ||||||
| chr12:7871355
|
G | A | 2 | a0001c0004t0001g0285a0001c0006t0009g0284 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-57-1418C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871355 | ||||||
| chr12:7871464
|
C | T | 1 | a0001c0002t0003g0079 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-58+1343G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871464 | ||||||
| chr12:7871500
|
C | T | 5 | a0001c0003t0001g0290a0001c0006t0004g0286a0001c0006t0004g0287others(2): Show | 5 | HG02622.hp2 HG02965.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+1307G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871500 | ||||||
| chr12:7871612
|
G | A | 135 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(132): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.-58+1195C>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871612 | ||||||
| chr12:7871699
|
C | T | 135 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(132): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.-58+1108G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871699 | ||||||
| chr12:7871766
|
T | C | 135 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(132): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.-58+1041A>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871766 | ||||||
| chr12:7871845
|
C | A | 76 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(73): Show | 76 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-58+962G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871845 | ||||||
| chr12:7871913
|
A | G | 1 | a0001c0004t0001g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-58+894T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871913 | ||||||
| chr12:7871975
|
A | G | 2 | a0002c0001t0002g0002a0002c0011t0008g0003 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-58+832T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871975 | ||||||
| chr12:7871988
|
A | G | 270 | a0001c0002t0003g0079a0001c0002t0003g0080a0001c0002t0003g0082others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.-58+819T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7871988 | ||||||
| chr12:7872313
|
G | C | 1 | a0001c0002t0003g0347 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-58+494C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7872313 | ||||||
| chr12:7872460
|
C | T | 1 | a0001c0007t0009g0078 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+347G>A | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7872460 | ||||||
| chr12:7872502
|
A | G | 1 | a0001c0003t0001g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+305T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7872502 | ||||||
| chr12:7872670
|
A | G | 76 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0022others(73): Show | 76 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-58+137T>C | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7872670 | ||||||
| chr12:7872675
|
C | A | 1 | a0001c0004t0001g0348 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-58+132G>T | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7872675 | ||||||
| chr12:7872770
|
G | C | 1 | a0001c0006t0004g0349 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-58+37C>G | SLC2A14 | ENSG00000173262.12 | transcript | ENST00000431042.7 | protein_coding | 1/10 | chr12 | 7872770 |