Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8140 |
|---|---|
| ensemblid | ENSG00000103257.9 |
| hgncid | 11063 |
| symbol | SLC7A5 |
| name | solute carrier family 7 member 5 |
| refseq_nuc | NM_003486.7 |
| refseq_prot | NP_003477.4 |
| ensembl_nuc | ENST00000261622.5 |
| ensembl_prot | ENSP00000261622.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 87830023 |
| end | 87869507 |
| strand | - |
| ver | v1.2 |
| region | chr16:87830023-87869507 |
| region5000 | chr16:87825023-87874507 |
| regionname0 | SLC7A5_chr16_87830023_87869507 |
| regionname5000 | SLC7A5_chr16_87825023_87874507 |
| 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 | 507 | 375 | 83 | 78 | 146 | 18 | 48 | 100 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0002 | 0/0 | 507 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0003 | 0/0 | 507 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0004 | 0/0 | 507 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0005 | 0/0 | 507 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0006 | 0/0 | 507 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0007 | 0/0 | 507 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0008 | 0/0 | 507 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1524 | 313 | 47 | 62 | 144 | 15 | 44 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0002 | 0/1 | 1524 | 48 | 34 | 7 | 0 | 3 | 3 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0003 | 0/0 | 1524 | 9 | 0 | 7 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0004 | 0/0 | 1524 | 4 | 4 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0005 | 0/0 | 1524 | 3 | 2 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0006 | 0/0 | 1524 | 3 | 3 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0007 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0008 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0009 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0010 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0011 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0012 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0013 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0014 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0015 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| c0016 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| 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 | 3036 | 99 | 4 | 26 | 59 | 4 | 6 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0002 | 1/1 | 3033 | 48 | 3 | 18 | 13 | 4 | 8 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0003 | 0/0 | 3032 | 22 | 1 | 2 | 12 | 0 | 7 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0004 | 0/0 | 3032 | 21 | 0 | 4 | 14 | 1 | 2 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0005 | 0/0 | 3032 | 20 | 2 | 4 | 8 | 2 | 4 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0006 | 0/0 | 3033 | 18 | 13 | 0 | 2 | 0 | 3 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0007 | 0/0 | 3033 | 12 | 0 | 1 | 3 | 3 | 5 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0008 | 0/0 | 3036 | 10 | 9 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0009 | 0/0 | 3036 | 9 | 0 | 0 | 9 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0010 | 0/0 | 3032 | 8 | 7 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0011 | 0/0 | 3036 | 7 | 0 | 2 | 3 | 1 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0012 | 0/0 | 3034 | 6 | 2 | 3 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0013 | 0/0 | 3032 | 6 | 0 | 0 | 0 | 1 | 5 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0014 | 0/0 | 3033 | 6 | 6 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0015 | 0/0 | 3034 | 6 | 0 | 0 | 6 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0016 | 0/0 | 3036 | 6 | 6 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0017 | 0/0 | 3034 | 5 | 5 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0018 | 0/0 | 3033 | 4 | 0 | 4 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0019 | 0/0 | 3034 | 3 | 3 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0020 | 0/0 | 3036 | 3 | 3 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0021 | 0/0 | 3033 | 3 | 0 | 0 | 3 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0022 | 0/0 | 3036 | 3 | 0 | 2 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0023 | 0/0 | 3033 | 3 | 3 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0024 | 0/0 | 3032 | 3 | 3 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0025 | 0/0 | 3032 | 3 | 0 | 1 | 1 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0026 | 0/0 | 3036 | 2 | 1 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0027 | 0/0 | 3036 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0028 | 0/0 | 3036 | 2 | 0 | 2 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0029 | 0/0 | 3036 | 2 | 0 | 2 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0030 | 0/0 | 3036 | 2 | 1 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0031 | 0/0 | 3036 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0032 | 0/0 | 3032 | 2 | 0 | 0 | 0 | 1 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0033 | 0/0 | 3036 | 2 | 0 | 0 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0034 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0035 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0036 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0037 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0038 | 0/0 | 3033 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0039 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0040 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0041 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0042 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0043 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0044 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0045 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0046 | 0/0 | 3032 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0047 | 0/0 | 3032 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0048 | 0/0 | 3032 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0049 | 0/0 | 3034 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0050 | 0/0 | 3033 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0051 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0052 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0053 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0054 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0055 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0056 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0057 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0058 | 0/0 | 3036 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0059 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0060 | 0/0 | 3036 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0061 | 0/0 | 3032 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0062 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0063 | 0/0 | 3036 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0064 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0065 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0066 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0067 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0068 | 0/0 | 3045 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0069 | 0/0 | 3036 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0070 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0071 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0072 | 0/0 | 3033 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| t0073 | 0/0 | 3032 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| 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 | 3 | 0 | 3 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0377 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1524 | 313 | 47 | 62 | 144 | 15 | 44 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002 | 0/1 | 1524 | 48 | 34 | 7 | 0 | 3 | 3 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0003 | 0/0 | 1524 | 9 | 0 | 7 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0005 | 0/0 | 1524 | 3 | 2 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0011 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0013 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0002c0004 | 0/0 | 1524 | 4 | 4 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0002c0016 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0003c0006 | 0/0 | 1524 | 3 | 3 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0004c0008 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0004c0014 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0004c0015 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0005c0009 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0006c0012 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0007c0010 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0008c0007 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4559 | 76 | 2 | 13 | 55 | 1 | 5 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0002 | 1/0 | 4556 | 44 | 3 | 16 | 13 | 4 | 7 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0003 | 0/0 | 4555 | 22 | 1 | 2 | 12 | 0 | 7 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0004 | 0/0 | 4555 | 21 | 0 | 4 | 14 | 1 | 2 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0005 | 0/0 | 4555 | 18 | 1 | 4 | 8 | 2 | 3 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0006 | 0/0 | 4556 | 10 | 5 | 0 | 2 | 0 | 3 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0007 | 0/0 | 4556 | 12 | 0 | 1 | 3 | 3 | 5 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0008 | 0/0 | 4559 | 4 | 3 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0009 | 0/0 | 4559 | 9 | 0 | 0 | 9 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0010 | 0/0 | 4555 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0011 | 0/0 | 4559 | 7 | 0 | 2 | 3 | 1 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0012 | 0/0 | 4557 | 4 | 1 | 2 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0013 | 0/0 | 4555 | 5 | 0 | 0 | 0 | 1 | 4 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0014 | 0/0 | 4556 | 5 | 5 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0015 | 0/0 | 4557 | 6 | 0 | 0 | 6 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0016 | 0/0 | 4559 | 5 | 5 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0017 | 0/0 | 4557 | 5 | 5 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0018 | 0/0 | 4556 | 4 | 0 | 4 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0020 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0021 | 0/0 | 4556 | 3 | 0 | 0 | 3 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0022 | 0/0 | 4559 | 3 | 0 | 2 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0023 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0024 | 0/0 | 4555 | 3 | 3 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0025 | 0/0 | 4555 | 3 | 0 | 1 | 1 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0026 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0028 | 0/0 | 4559 | 2 | 0 | 2 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0029 | 0/0 | 4559 | 2 | 0 | 2 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0030 | 0/0 | 4559 | 2 | 1 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0032 | 0/0 | 4555 | 2 | 0 | 0 | 0 | 1 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0033 | 0/0 | 4559 | 2 | 0 | 0 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0034 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0036 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0037 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0038 | 0/0 | 4556 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0040 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0046 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0047 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0048 | 0/0 | 4555 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0049 | 0/0 | 4557 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0050 | 0/0 | 4556 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0051 | 0/0 | 4556 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0052 | 0/0 | 4556 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0053 | 0/0 | 4556 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0054 | 0/0 | 4552 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0056 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0057 | 0/0 | 4557 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0058 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0059 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0060 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0061 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0062 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0065 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0067 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0068 | 0/0 | 4568 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0069 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0070 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0071 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0072 | 0/0 | 4556 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0001t0073 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0001 | 0/0 | 4559 | 10 | 2 | 5 | 0 | 3 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0002 | 0/1 | 4556 | 3 | 0 | 1 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0005 | 0/0 | 4555 | 2 | 1 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0006 | 0/0 | 4556 | 8 | 8 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0008 | 0/0 | 4559 | 4 | 4 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0010 | 0/0 | 4555 | 6 | 5 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0012 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0013 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0016 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0020 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0023 | 0/0 | 4556 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0026 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0027 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0039 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0041 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0045 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0055 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0002t0066 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0003t0001 | 0/0 | 4559 | 9 | 0 | 7 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0005t0031 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0005t0063 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0011t0001 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0001c0013t0012 | 0/0 | 4557 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0002c0004t0019 | 0/0 | 4557 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0002c0004t0043 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0002c0004t0044 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0002c0016t0019 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0003c0006t0008 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0003c0006t0014 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0004c0008t0064 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0004c0014t0035 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0004c0015t0042 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0005c0009t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0006c0012t0002 | 0/0 | 4556 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0007c0010t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| a0008c0007t0001 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | copy fasta | chr16 | 87825023 | 87874507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0003g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0006g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0007g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0007g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0007g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0007g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0007g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0007g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0007g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0007g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0007g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0007g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0007g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0007g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0008g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0008g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0009g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0009g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0009g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0009g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0009g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0009g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0010g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0010g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0011g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0011g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0011g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0011g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0011g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0011g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0011g0377 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0012g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0012g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0012g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0012g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0013g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0013g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0013g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0013g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0013g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0014g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0014g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0014g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0014g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0015g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0015g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0015g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0015g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0015g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0015g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0016g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0016g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0016g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0016g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0016g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0017g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0017g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0017g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0017g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0017g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0018g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0018g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0018g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0018g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0020g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0021g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0021g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0021g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0022g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0022g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0022g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0023g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0024g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0024g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0024g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0025g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0025g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0025g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0026g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0028g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0028g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0029g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0029g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0030g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0030g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0032g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0032g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0033g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0033g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0034g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0036g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0037g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0038g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0040g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0046g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0047g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0048g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0049g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0050g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0051g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0052g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0053g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0054g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0056g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0057g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0058g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0059g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0060g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0061g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0062g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0065g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0067g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0068g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0069g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0070g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0071g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0072g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0001t0073g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0002g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0005g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0008g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0010g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0013g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0016g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0020g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0020g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0023g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0023g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0026g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0027g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0027g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0039g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0041g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0045g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0055g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0002t0066g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0005t0031g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0005t0031g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0005t0063g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0011t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0001c0013t0012g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0002c0004t0019g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0002c0004t0019g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0002c0004t0043g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0002c0004t0044g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0002c0016t0019g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0003c0006t0008g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0003c0006t0008g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0003c0006t0014g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0004c0008t0064g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0004c0014t0035g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0004c0015t0042g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0005c0009t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0006c0012t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0007c0010t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| a0008c0007t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0018 | EUR | GBR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0182 | EUR | GBR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0013 | EUR | GBR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | GBR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0284 | EUR | FIN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0283 | EUR | FIN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0020 | EUR | FIN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00323 | hp2 | a0001 | c0001 | t0032 | g0348 | EUR | FIN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00408 | hp2 | a0001 | c0001 | t0009 | g0220 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0205 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00438 | hp2 | a0001 | c0001 | t0011 | g0376 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00597 | hp2 | a0001 | c0001 | t0021 | g0253 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00609 | hp1 | a0001 | c0001 | t0021 | g0201 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00639 | hp2 | a0001 | c0002 | t0010 | g0011 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0166 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00673 | hp2 | a0001 | c0001 | t0033 | g0380 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00733 | hp2 | a0001 | c0001 | t0038 | g0189 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00735 | hp2 | a0001 | c0001 | t0022 | g0184 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0333 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01070 | hp1 | a0001 | c0001 | t0011 | g0325 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01070 | hp2 | a0001 | c0001 | t0018 | g0314 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01071 | hp2 | a0001 | c0001 | t0018 | g0313 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01074 | hp1 | a0001 | c0001 | t0030 | g0311 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0148 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01081 | hp2 | a0001 | c0005 | t0063 | g0382 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01106 | hp2 | a0001 | c0001 | t0050 | g0057 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01109 | hp1 | a0001 | c0001 | t0012 | g0060 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01109 | hp2 | a0001 | c0001 | t0018 | g0315 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0144 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01167 | hp2 | a0001 | c0001 | t0026 | g0126 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0378 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0186 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01192 | hp2 | a0001 | c0001 | t0028 | g0231 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0131 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01256 | hp1 | a0001 | c0013 | t0012 | g0165 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01256 | hp2 | a0001 | c0001 | t0029 | g0162 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01258 | hp1 | a0001 | c0001 | t0029 | g0161 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0294 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01346 | hp2 | a0001 | c0001 | t0048 | g0224 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01358 | hp1 | a0001 | c0001 | t0025 | g0326 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01358 | hp2 | a0006 | c0012 | t0002 | g0292 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0101 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01433 | hp1 | a0001 | c0001 | t0022 | g0170 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0137 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01515 | hp1 | a0001 | c0001 | t0022 | g0183 | EUR | IBS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01515 | hp2 | a0001 | c0001 | t0007 | g0344 | EUR | IBS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0187 | EUR | IBS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01516 | hp2 | a0001 | c0001 | t0011 | g0377 | EUR | IBS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0188 | EUR | IBS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01517 | hp2 | a0001 | c0001 | t0007 | g0345 | EUR | IBS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01884 | hp2 | a0001 | c0002 | t0006 | g0025 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01891 | hp1 | a0001 | c0001 | t0016 | g0289 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01891 | hp2 | a0001 | c0002 | t0023 | g0317 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0102 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0099 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0054 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0136 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0114 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01981 | hp1 | a0001 | c0001 | t0060 | g0141 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0338 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0125 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02004 | hp2 | a0001 | c0001 | t0028 | g0230 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0291 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02015 | hp2 | a0001 | c0001 | t0012 | g0268 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0206 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02055 | hp1 | a0001 | c0001 | t0016 | g0285 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02055 | hp2 | a0001 | c0002 | t0039 | g0047 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0330 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0070 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02083 | hp1 | a0001 | c0001 | t0054 | g0094 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02132 | hp1 | a0001 | c0001 | t0070 | g0368 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02145 | hp1 | a0001 | c0002 | t0027 | g0016 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02145 | hp2 | a0001 | c0001 | t0023 | g0352 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0371 | EAS | CDX | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | CDX | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0372 | EAS | CDX | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02257 | hp1 | a0001 | c0001 | t0030 | g0312 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02258 | hp2 | a0001 | c0001 | t0020 | g0227 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0100 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02273 | hp2 | a0001 | c0001 | t0018 | g0316 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02280 | hp1 | a0001 | c0002 | t0006 | g0026 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0129 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02293 | hp1 | a0001 | c0001 | t0011 | g0337 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02293 | hp2 | a0008 | c0007 | t0001 | g0007 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02451 | hp1 | a0004 | c0015 | t0042 | g0056 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02451 | hp2 | a0001 | c0001 | t0016 | g0287 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02572 | hp1 | a0001 | c0002 | t0026 | g0014 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02572 | hp2 | a0001 | c0001 | t0016 | g0304 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02602 | hp1 | a0001 | c0001 | t0011 | g0322 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02615 | hp1 | a0001 | c0002 | t0020 | g0028 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02615 | hp2 | a0003 | c0006 | t0008 | g0309 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02622 | hp1 | a0001 | c0001 | t0062 | g0353 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02622 | hp2 | a0003 | c0006 | t0014 | g0308 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02630 | hp1 | a0001 | c0002 | t0010 | g0040 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02630 | hp2 | a0002 | c0004 | t0044 | g0043 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02647 | hp1 | a0001 | c0002 | t0016 | g0032 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02647 | hp2 | a0001 | c0001 | t0037 | g0092 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0357 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02717 | hp1 | a0001 | c0002 | t0010 | g0046 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0354 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02723 | hp2 | a0001 | c0001 | t0024 | g0359 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02738 | hp1 | a0001 | c0001 | t0013 | g0155 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02809 | hp1 | a0003 | c0006 | t0008 | g0310 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02809 | hp2 | a0001 | c0001 | t0024 | g0356 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02818 | hp1 | a0002 | c0004 | t0043 | g0041 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0288 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02886 | hp1 | a0001 | c0002 | t0010 | g0034 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0059 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02897 | hp1 | a0001 | c0002 | t0010 | g0039 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02897 | hp2 | a0001 | c0001 | t0014 | g0261 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02922 | hp1 | a0001 | c0002 | t0008 | g0015 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02922 | hp2 | a0001 | c0002 | t0041 | g0036 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02965 | hp1 | a0001 | c0001 | t0067 | g0324 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0130 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02970 | hp1 | a0002 | c0016 | t0019 | g0263 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02970 | hp2 | a0001 | c0005 | t0031 | g0381 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02976 | hp1 | a0001 | c0002 | t0006 | g0027 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0128 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03017 | hp1 | a0001 | c0011 | t0001 | g0115 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03017 | hp2 | a0001 | c0001 | t0025 | g0334 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03041 | hp1 | a0001 | c0001 | t0017 | g0208 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03041 | hp2 | a0001 | c0002 | t0010 | g0031 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03098 | hp1 | a0001 | c0002 | t0012 | g0050 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03098 | hp2 | a0001 | c0002 | t0006 | g0024 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0066 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0298 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03139 | hp2 | a0001 | c0001 | t0024 | g0355 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0259 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03195 | hp2 | a0001 | c0001 | t0017 | g0120 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03209 | hp1 | a0004 | c0014 | t0035 | g0005 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0052 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03225 | hp1 | a0002 | c0004 | t0019 | g0044 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03225 | hp2 | a0001 | c0002 | t0055 | g0030 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0329 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0079 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03453 | hp1 | a0001 | c0001 | t0073 | g0385 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03453 | hp2 | a0001 | c0001 | t0017 | g0307 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03491 | hp1 | a0001 | c0001 | t0007 | g0343 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03491 | hp2 | a0001 | c0001 | t0069 | g0323 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03492 | hp2 | a0001 | c0001 | t0007 | g0342 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03516 | hp1 | a0001 | c0002 | t0005 | g0009 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03516 | hp2 | a0001 | c0001 | t0017 | g0055 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03540 | hp1 | a0001 | c0002 | t0006 | g0023 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03540 | hp2 | a0001 | c0002 | t0006 | g0045 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03579 | hp1 | a0004 | c0008 | t0064 | g0319 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03579 | hp2 | a0001 | c0001 | t0034 | g0006 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0168 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0098 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0341 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0362 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0321 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0117 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03710 | hp1 | a0001 | c0001 | t0072 | g0384 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03710 | hp2 | a0001 | c0001 | t0049 | g0156 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03831 | hp1 | a0001 | c0001 | t0061 | g0335 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03831 | hp2 | a0001 | c0002 | t0013 | g0008 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03834 | hp1 | a0001 | c0002 | t0005 | g0049 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0225 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03927 | hp1 | a0001 | c0001 | t0013 | g0282 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0358 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0299 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0346 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG04115 | hp2 | a0001 | c0001 | t0032 | g0347 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0364 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG04184 | hp2 | a0001 | c0001 | t0013 | g0154 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0306 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0106 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0191 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG04228 | hp1 | a0001 | c0001 | t0058 | g0175 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0332 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18522 | hp1 | a0002 | c0004 | t0019 | g0010 | AFR | YRI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18522 | hp2 | a0001 | c0002 | t0066 | g0320 | AFR | YRI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18612 | hp1 | a0001 | c0001 | t0021 | g0254 | EAS | CHB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | CHB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18747 | hp1 | a0001 | c0001 | t0007 | g0361 | EAS | CHB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | CHB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18906 | hp1 | a0001 | c0002 | t0006 | g0002 | AFR | YRI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18906 | hp2 | a0001 | c0002 | t0008 | g0038 | AFR | YRI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0366 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18944 | hp1 | a0001 | c0001 | t0025 | g0351 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18948 | hp1 | a0001 | c0001 | t0015 | g0064 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18950 | hp2 | a0001 | c0001 | t0056 | g0110 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18953 | hp2 | a0001 | c0001 | t0005 | g0132 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18957 | hp1 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18957 | hp2 | a0001 | c0001 | t0047 | g0210 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18959 | hp2 | a0001 | c0001 | t0009 | g0116 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0370 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18964 | hp1 | a0001 | c0001 | t0015 | g0199 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0363 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18966 | hp1 | a0001 | c0001 | t0015 | g0063 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18970 | hp2 | a0001 | c0001 | t0009 | g0104 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0367 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18980 | hp2 | a0001 | c0001 | t0009 | g0293 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18982 | hp2 | a0001 | c0001 | t0006 | g0271 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18983 | hp2 | a0001 | c0001 | t0007 | g0331 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18986 | hp2 | a0001 | c0001 | t0059 | g0173 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18988 | hp1 | a0001 | c0001 | t0009 | g0088 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18989 | hp2 | a0001 | c0001 | t0009 | g0209 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18998 | hp1 | a0001 | c0001 | t0052 | g0078 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0365 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19002 | hp2 | a0001 | c0001 | t0057 | g0228 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19003 | hp1 | a0001 | c0001 | t0009 | g0222 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19004 | hp1 | a0001 | c0001 | t0051 | g0090 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19004 | hp2 | a0001 | c0001 | t0015 | g0062 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19005 | hp1 | a0001 | c0001 | t0071 | g0340 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19007 | hp1 | a0001 | c0001 | t0053 | g0091 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19007 | hp2 | a0001 | c0001 | t0011 | g0375 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19030 | hp1 | a0001 | c0001 | t0017 | g0109 | AFR | LWK | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0267 | AFR | LWK | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19043 | hp1 | a0001 | c0002 | t0008 | g0042 | AFR | LWK | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19043 | hp2 | a0001 | c0002 | t0023 | g0318 | AFR | LWK | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19060 | hp2 | a0001 | c0001 | t0046 | g0122 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19063 | hp1 | a0001 | c0001 | t0015 | g0160 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0350 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19064 | hp1 | a0001 | c0001 | t0015 | g0193 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19064 | hp2 | a0001 | c0001 | t0007 | g0349 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19066 | hp1 | a0001 | c0001 | t0011 | g0369 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19066 | hp2 | a0001 | c0001 | t0009 | g0221 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19070 | hp2 | a0001 | c0001 | t0009 | g0169 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0373 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19074 | hp2 | a0005 | c0009 | t0001 | g0218 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19081 | hp2 | a0007 | c0010 | t0001 | g0211 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19090 | hp1 | a0001 | c0001 | t0068 | g0379 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19091 | hp1 | a0001 | c0001 | t0033 | g0360 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19240 | hp1 | a0001 | c0002 | t0027 | g0017 | AFR | YRI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA19240 | hp2 | a0001 | c0005 | t0031 | g0383 | AFR | YRI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA20129 | hp1 | a0001 | c0002 | t0045 | g0033 | AFR | ASW | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA20129 | hp2 | a0001 | c0002 | t0008 | g0037 | AFR | ASW | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA20752 | hp1 | a0001 | c0001 | t0007 | g0328 | EUR | TSI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA20752 | hp2 | a0001 | c0001 | t0013 | g0275 | EUR | TSI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0185 | EUR | TSI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0084 | EUR | TSI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0327 | SAS | GIH | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA20905 | hp2 | a0001 | c0001 | t0013 | g0167 | SAS | GIH | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0145 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0164 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02486 | hp1 | a0001 | c0002 | t0006 | g0002 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0146 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG02559 | hp2 | a0001 | c0002 | t0020 | g0029 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0260 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG03471 | hp2 | a0001 | c0001 | t0040 | g0163 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG06807 | hp1 | a0001 | c0001 | t0014 | g0262 | AFR | USA | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | USA | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA20300 | hp1 | a0001 | c0001 | t0016 | g0286 | AFR | USA | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | USA | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA21309 | hp1 | a0001 | c0001 | t0036 | g0061 | AFR | LWK | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| NA21309 | hp2 | a0001 | c0001 | t0065 | g0374 | AFR | LWK | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0048 | REF | REF | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0281 | REF | REF | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:87834456
|
C | A | 1 | a0006 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.1426G>T | p.Val476Phe | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/10 | 1511/4556 | 1426/1524 | 476/507 | chr16 | 87834456 | ||
| chr16:87836614
|
C | T | 1 | a0007 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.1174G>A | p.Asp392Asn | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/10 | 1259/4556 | 1174/1524 | 392/507 | chr16 | 87836614 | ||
| chr16:87841130
|
G | C | 1 | a0004 | 3 | HG02451.hp1 HG03209.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.690C>G | p.Asn230Lys | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/10 | 775/4556 | 690/1524 | 230/507 | chr16 | 87841130 | ||
| chr16:87841152
|
T | A | 1 | a0002 | 5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.668A>T | p.Asp223Val | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/10 | 753/4556 | 668/1524 | 223/507 | chr16 | 87841152 | ||
| chr16:87851804
|
C | T | 1 | a0005 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.584G>A | p.Arg195Gln | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/10 | 669/4556 | 584/1524 | 195/507 | chr16 | 87851804 | ||
| chr16:87869155
|
C | T | 1 | a0008 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.268G>A | p.Ala90Thr | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | 353/4556 | 268/1524 | 90/507 | chr16 | 87869155 | ||
| chr16:87869406
|
G | A | 1 | a0003 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.17C>T | p.Pro6Leu | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | 102/4556 | 17/1524 | 6/507 | chr16 | 87869406 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:87833024
|
G | A | 1 | a0001c0011 | 1 | HG03017.hp1 | splice_region_variant&synonymous_variant | LOW | c.1470C>T | p.Phe490Phe | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1555/4556 | 1470/1524 | 490/507 | chr16 | 87833024 | ||
| chr16:87834535
|
G | C | 1 | a0001c0003 | 9 | HG01261.hp2 HG01496.hp1 HG01928.hp1 others(6): Show |
synonymous_variant | LOW | c.1347C>G | p.Val449Val | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/10 | 1432/4556 | 1347/1524 | 449/507 | chr16 | 87834535 | ||
| chr16:87837854
|
G | A | 1 | a0001c0013 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.1131C>T | p.Leu377Leu | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/10 | 1216/4556 | 1131/1524 | 377/507 | chr16 | 87837854 | ||
| chr16:87838749
|
G | A | 2 | a0004c0008a0004c0015 | 2 | HG02451.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.1008C>T | p.Phe336Phe | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/10 | 1093/4556 | 1008/1524 | 336/507 | chr16 | 87838749 | ||
| chr16:87869036
|
G | A | 1 | a0001c0005 | 3 | HG01081.hp2 HG02970.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.387C>T | p.Ala129Ala | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | 472/4556 | 387/1524 | 129/507 | chr16 | 87869036 | ||
| chr16:87869078
|
G | T | 4 | a0001c0002a0002c0004a0003c0006others(1): Show | 56 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(53): Show |
synonymous_variant | LOW | c.345C>A | p.Gly115Gly | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | 430/4556 | 345/1524 | 115/507 | chr16 | 87869078 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:87830134
|
C | T | 7 | a0001c0001t0008a0001c0002t0008a0001c0002t0066others(4): Show | 15 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2836G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2836 | chr16 | 87830134 | |||||
| chr16:87830196
|
G | A | 1 | a0001c0001t0047 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2774C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2774 | chr16 | 87830196 | |||||
| chr16:87830236
|
T | C | 1 | a0001c0001t0053 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2734A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2734 | chr16 | 87830236 | |||||
| chr16:87830334
|
C | G | 1 | a0001c0001t0038 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2636G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2636 | chr16 | 87830334 | |||||
| chr16:87830396
|
A | T | 1 | a0001c0001t0061 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2574T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2574 | chr16 | 87830396 | |||||
| chr16:87830468
|
A | G | 18 | a0001c0001t0006a0001c0001t0014a0001c0001t0017others(15): Show | 44 | HG00733.hp2 HG01884.hp2 HG01891.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2502T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2502 | chr16 | 87830468 | |||||
| chr16:87830597
|
T | C | 1 | a0001c0001t0068 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2373A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2373 | chr16 | 87830597 | |||||
| chr16:87830663
|
G | A | 5 | a0001c0001t0005a0001c0001t0025a0001c0001t0054others(2): Show | 25 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2307C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2307 | chr16 | 87830663 | |||||
| chr16:87830672
|
C | A | 2 | a0002c0004t0043a0004c0008t0064 | 2 | HG02818.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2298G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2298 | chr16 | 87830672 | |||||
| chr16:87830718
|
C | T | 1 | a0002c0004t0043 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2252G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2252 | chr16 | 87830718 | |||||
| chr16:87830743
|
C | A | 2 | a0001c0001t0067a0001c0002t0027 | 3 | HG02145.hp1 HG02965.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2227G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2227 | chr16 | 87830743 | |||||
| chr16:87830812
|
G | T | 9 | a0001c0001t0008a0001c0001t0067a0001c0002t0008others(6): Show | 18 | HG01167.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2158C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2158 | chr16 | 87830812 | |||||
| chr16:87830826
|
G | A | 1 | a0004c0008t0064 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2144C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2144 | chr16 | 87830826 | |||||
| chr16:87830869
|
G | C | 42 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(39): Show | 160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*2101C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2101 | chr16 | 87830869 | |||||
| chr16:87830877
|
G | A | 12 | a0001c0001t0008a0001c0001t0020a0001c0001t0026others(9): Show | 21 | HG01081.hp2 HG01167.hp1 HG01167.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2093C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2093 | chr16 | 87830877 | |||||
| chr16:87830877
|
G | T | 1 | a0001c0001t0052 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2093 | chr16 | 87830877 | |||||
| chr16:87830938
|
C | T | 1 | a0001c0001t0051 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2032G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2032 | chr16 | 87830938 | |||||
| chr16:87830950
|
G | A | 1 | a0001c0001t0069 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2020C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2020 | chr16 | 87830950 | |||||
| chr16:87831015
|
C | T | 14 | a0001c0001t0010a0001c0001t0020a0001c0001t0024others(11): Show | 23 | HG00639.hp2 HG01081.hp2 HG01167.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1955G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1955 | chr16 | 87831015 | |||||
| chr16:87831048
|
C | T | 1 | a0001c0001t0058 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1922G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1922 | chr16 | 87831048 | |||||
| chr16:87831060
|
C | T | 1 | a0001c0001t0046 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1910G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1910 | chr16 | 87831060 | |||||
| chr16:87831075
|
C | A | 1 | a0001c0001t0028 | 2 | HG01192.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1895G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1895 | chr16 | 87831075 | |||||
| chr16:87831090
|
C | T | 1 | a0001c0001t0021 | 3 | HG00597.hp2 HG00609.hp1 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1880G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1880 | chr16 | 87831090 | |||||
| chr16:87831145
|
A | C | 1 | a0001c0001t0068 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1825T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1825 | chr16 | 87831145 | |||||
| chr16:87831145
|
AAC | A | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(15): Show | 97 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1823_*1824delGT | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1823 | chr16 | 87831145 | |||||
| chr16:87831192
|
G | A | 1 | a0004c0008t0064 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1778C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1778 | chr16 | 87831192 | |||||
| chr16:87831196
|
G | A | 2 | a0001c0001t0029a0001c0001t0070 | 3 | HG01256.hp2 HG01258.hp1 HG02132.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1774C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1774 | chr16 | 87831196 | |||||
| chr16:87831233
|
G | A | 1 | a0001c0001t0059 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1737C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1737 | chr16 | 87831233 | |||||
| chr16:87831243
|
C | T | 1 | a0001c0001t0022 | 3 | HG00735.hp2 HG01433.hp1 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1727G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1727 | chr16 | 87831243 | |||||
| chr16:87831279
|
C | A | 2 | a0002c0004t0043a0002c0004t0044 | 2 | HG02630.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1691G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1691 | chr16 | 87831279 | |||||
| chr16:87831334
|
C | T | 1 | a0001c0002t0041 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1636G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1636 | chr16 | 87831334 | |||||
| chr16:87831416
|
C | T | 48 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(45): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1554G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1554 | chr16 | 87831416 | |||||
| chr16:87831428
|
G | C | 1 | a0001c0001t0040 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1542C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1542 | chr16 | 87831428 | |||||
| chr16:87831433
|
A | G | 2 | a0001c0001t0016a0001c0002t0016 | 6 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1537T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1537 | chr16 | 87831433 | |||||
| chr16:87831491
|
C | T | 2 | a0002c0004t0043a0002c0004t0044 | 2 | HG02630.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1479G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1479 | chr16 | 87831491 | |||||
| chr16:87831492
|
G | A | 1 | a0004c0008t0064 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1478C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1478 | chr16 | 87831492 | |||||
| chr16:87831515
|
GAC | G | 29 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(26): Show | 110 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1453_*1454delGT | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1453 | chr16 | 87831515 | |||||
| chr16:87831595
|
T | A | 9 | a0001c0001t0005a0001c0001t0013a0001c0001t0025others(6): Show | 34 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1375A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1375 | chr16 | 87831595 | |||||
| chr16:87831619
|
G | A | 2 | a0001c0001t0065a0004c0015t0042 | 2 | HG02451.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1351C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1351 | chr16 | 87831619 | |||||
| chr16:87831638
|
C | G | 1 | a0001c0002t0055 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1332G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1332 | chr16 | 87831638 | |||||
| chr16:87831643
|
C | T | 1 | a0001c0001t0050 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1327G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1327 | chr16 | 87831643 | |||||
| chr16:87831663
|
C | CGGG | 71 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(68): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*1304_*1306dupCCC | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1306 | chr16 | 87831663 | |||||
| chr16:87831688
|
C | T | 44 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(41): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*1282G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1282 | chr16 | 87831688 | |||||
| chr16:87831735
|
T | C | 1 | a0001c0002t0041 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1235A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1235 | chr16 | 87831735 | |||||
| chr16:87831902
|
A | T | 2 | a0002c0004t0043a0002c0004t0044 | 2 | HG02630.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1068T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1068 | chr16 | 87831902 | |||||
| chr16:87831953
|
G | A | 1 | a0001c0002t0055 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1017C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1017 | chr16 | 87831953 | |||||
| chr16:87831995
|
G | A | 1 | a0001c0001t0060 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*975C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 975 | chr16 | 87831995 | |||||
| chr16:87832086
|
G | T | 4 | a0002c0004t0019a0002c0004t0043a0002c0004t0044others(1): Show | 5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*884C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 884 | chr16 | 87832086 | |||||
| chr16:87832225
|
C | T | 1 | a0001c0001t0056 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*745G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 745 | chr16 | 87832225 | |||||
| chr16:87832313
|
G | A | 2 | a0001c0001t0016a0001c0002t0016 | 6 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*657C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 657 | chr16 | 87832313 | |||||
| chr16:87832342
|
G | A | 2 | a0001c0001t0071a0001c0002t0055 | 2 | HG03225.hp2 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*628C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 628 | chr16 | 87832342 | |||||
| chr16:87832391
|
C | T | 1 | a0001c0001t0018 | 4 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*579G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 579 | chr16 | 87832391 | |||||
| chr16:87832477
|
C | CGAATGTC others(4): Show |
1 | a0001c0001t0068 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*482_*492dupTTGTGA others(5): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 492 | chr16 | 87832477 | |||||
| chr16:87832501
|
G | T | 2 | a0001c0001t0065a0004c0015t0042 | 2 | HG02451.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*469C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 469 | chr16 | 87832501 | |||||
| chr16:87832512
|
C | T | 12 | a0001c0001t0008a0001c0001t0026a0001c0001t0034others(9): Show | 20 | HG01081.hp2 HG01167.hp1 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*458G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 458 | chr16 | 87832512 | |||||
| chr16:87832532
|
G | C | 26 | a0001c0001t0001a0001c0001t0009a0001c0001t0011others(23): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*438C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 438 | chr16 | 87832532 | |||||
| chr16:87832681
|
A | T | 11 | a0001c0001t0006a0001c0001t0023a0001c0001t0037others(8): Show | 29 | HG00733.hp2 HG01884.hp2 HG01891.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*289T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 289 | chr16 | 87832681 | |||||
| chr16:87832768
|
TGG | T | 2 | a0002c0004t0019a0002c0016t0019 | 3 | HG02970.hp1 HG03225.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*200_*201delCC | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 200 | chr16 | 87832768 | |||||
| chr16:87832894
|
C | T | 1 | a0001c0001t0036 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*76G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 76 | chr16 | 87832894 | |||||
| chr16:87869453
|
C | G | 2 | a0001c0001t0034a0004c0014t0035 | 2 | HG03209.hp1 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-31G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | 31 | chr16 | 87869453 | |||||
| chr16:87869471
|
G | A | 3 | a0001c0001t0018a0001c0001t0030a0001c0001t0073 | 7 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-49C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | chr16 | 87869471 | ||||||
| chr16:87869471
|
G | C | 1 | a0001c0001t0072 | 1 | HG03710.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-49C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | chr16 | 87869471 | ||||||
| chr16:87869476
|
G | C | 23 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(20): Show | 69 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(66): Show |
5_prime_UTR_variant | MODIFIER | c.-54C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | 54 | chr16 | 87869476 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:87833084
|
C | T | 3 | a0001c0001t0020g0227a0001c0002t0020g0028a0001c0002t0020g0029 | 3 | HG02258.hp2 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1469-59G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833084 | ||||||
| chr16:87833128
|
C | T | 1 | a0005c0009t0001g0218 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1469-103G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833128 | ||||||
| chr16:87833133
|
G | A | 13 | a0001c0001t0008g0144a0001c0001t0008g0145a0001c0001t0008g0146others(10): Show | 13 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1469-108C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833133 | ||||||
| chr16:87833138
|
T | C | 1 | a0001c0001t0061g0335 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1469-113A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833138 | ||||||
| chr16:87833182
|
G | C | 2 | a0001c0001t0065g0374a0004c0015t0042g0056 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1469-157C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833182 | ||||||
| chr16:87833193
|
C | T | 1 | a0001c0001t0030g0312 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1469-168G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833193 | ||||||
| chr16:87833195
|
G | A | 1 | a0001c0001t0004g0238 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1469-170C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833195 | ||||||
| chr16:87833204
|
A | G | 6 | a0001c0001t0026g0126a0001c0001t0034g0006a0001c0001t0040g0163others(3): Show | 6 | HG01081.hp2 HG01167.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469-179T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833204 | ||||||
| chr16:87833252
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1469-227G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833252 | ||||||
| chr16:87833259
|
C | T | 2 | a0001c0001t0002g0074a0001c0001t0002g0076 | 2 | HG01099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1469-234G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833259 | ||||||
| chr16:87833275
|
C | T | 2 | a0001c0001t0003g0341a0001c0001t0003g0346 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1469-250G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833275 | ||||||
| chr16:87833291
|
C | T | 3 | a0002c0004t0019g0010a0002c0004t0019g0044a0002c0016t0019g0263 | 3 | HG02970.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1469-266G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833291 | ||||||
| chr16:87833308
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1469-283C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833308 | ||||||
| chr16:87833420
|
G | C | 1 | a0001c0001t0012g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1469-395C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833420 | ||||||
| chr16:87833424
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1469-399C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833424 | ||||||
| chr16:87833463
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1469-438G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833463 | ||||||
| chr16:87833509
|
G | A | 19 | a0001c0001t0002g0075a0001c0001t0002g0077a0001c0001t0002g0087others(16): Show | 19 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.1469-484C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833509 | ||||||
| chr16:87833534
|
G | A | 2 | a0001c0001t0004g0114a0001c0001t0004g0283 | 2 | HG00280.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1469-509C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833534 | ||||||
| chr16:87833540
|
A | C | 5 | a0002c0004t0019g0010a0002c0004t0019g0044a0002c0004t0043g0041others(2): Show | 5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469-515T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833540 | ||||||
| chr16:87833618
|
G | A | 16 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250others(13): Show | 16 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1469-593C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833618 | ||||||
| chr16:87833631
|
TGGGGTAG others(6): Show |
T | 40 | a0001c0001t0008g0144a0001c0001t0008g0145a0001c0001t0008g0146others(37): Show | 40 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.1469-619_1469-607d others(15): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833631 | ||||||
| chr16:87833642
|
T | C | 19 | a0001c0001t0006g0128a0001c0001t0006g0129a0001c0001t0006g0130others(16): Show | 19 | HG00733.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1469-617A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833642 | ||||||
| chr16:87833724
|
G | A | 1 | a0001c0001t0015g0193 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1468+690C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833724 | ||||||
| chr16:87833775
|
G | A | 8 | a0001c0001t0012g0059a0001c0001t0012g0060a0001c0001t0017g0109others(5): Show | 8 | HG01109.hp1 HG01256.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1468+639C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833775 | ||||||
| chr16:87833789
|
G | C | 1 | a0001c0001t0037g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1468+625C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833789 | ||||||
| chr16:87833803
|
C | T | 1 | a0001c0001t0012g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1468+611G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833803 | ||||||
| chr16:87833818
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1468+596G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833818 | ||||||
| chr16:87833841
|
G | A | 1 | a0001c0002t0001g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1468+573C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833841 | ||||||
| chr16:87833857
|
CT | C | 205 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(202): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1468+556delA | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833857 | ||||||
| chr16:87833896
|
C | T | 1 | a0001c0001t0006g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1468+518G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833896 | ||||||
| chr16:87833901
|
T | C | 1 | a0001c0001t0003g0378 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1468+513A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833901 | ||||||
| chr16:87833910
|
A | G | 1 | a0001c0001t0003g0378 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1468+504T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833910 | ||||||
| chr16:87833914
|
T | C | 1 | a0001c0001t0003g0378 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1468+500A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833914 | ||||||
| chr16:87833939
|
C | T | 1 | a0001c0001t0003g0378 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1468+475G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833939 | ||||||
| chr16:87833940
|
G | A | 4 | a0001c0001t0006g0066a0001c0002t0006g0002a0001c0002t0006g0045others(1): Show | 5 | HG02055.hp2 HG02486.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1468+474C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833940 | ||||||
| chr16:87833941
|
T | C | 1 | a0001c0001t0003g0378 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1468+473A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833941 | ||||||
| chr16:87833985
|
C | T | 94 | a0001c0001t0002g0105a0001c0001t0002g0195a0001c0001t0003g0330others(91): Show | 94 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1468+429G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833985 | ||||||
| chr16:87834043
|
A | G | 18 | a0001c0001t0012g0131a0001c0001t0017g0055a0001c0001t0017g0120others(15): Show | 18 | HG01081.hp2 HG01167.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1468+371T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87834043 | ||||||
| chr16:87834176
|
G | A | 10 | a0001c0001t0012g0131a0001c0001t0026g0126a0001c0001t0034g0006others(7): Show | 10 | HG01081.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1468+238C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87834176 | ||||||
| chr16:87834196
|
C | G | 5 | a0002c0004t0019g0010a0002c0004t0019g0044a0002c0004t0043g0041others(2): Show | 5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1468+218G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87834196 | ||||||
| chr16:87834266
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(138): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1468+148C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87834266 | ||||||
| chr16:87834344
|
G | A | 1 | a0004c0008t0064g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1468+70C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87834344 | ||||||
| chr16:87834403
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1468+11C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87834403 | ||||||
| chr16:87834689
|
C | T | 2 | a0001c0001t0004g0117a0001c0001t0004g0191 | 2 | HG03704.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1291-98G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87834689 | ||||||
| chr16:87834747
|
G | A | 1 | a0001c0001t0034g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1291-156C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87834747 | ||||||
| chr16:87834856
|
C | T | 35 | a0001c0001t0002g0105a0001c0001t0002g0195a0001c0001t0005g0058others(32): Show | 35 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1291-265G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87834856 | ||||||
| chr16:87834921
|
C | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(138): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1291-330G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87834921 | ||||||
| chr16:87834991
|
C | T | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1291-400G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87834991 | ||||||
| chr16:87835084
|
C | T | 6 | a0001c0001t0073g0385a0002c0004t0019g0010a0002c0004t0019g0044others(3): Show | 6 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291-493G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835084 | ||||||
| chr16:87835224
|
T | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(142): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1291-633A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835224 | ||||||
| chr16:87835225
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(138): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1291-634C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835225 | ||||||
| chr16:87835259
|
C | A | 1 | a0001c0001t0009g0116 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1291-668G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835259 | ||||||
| chr16:87835276
|
G | T | 1 | a0001c0001t0001g0239 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1291-685C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835276 | ||||||
| chr16:87835335
|
G | A | 2 | a0001c0001t0028g0230a0001c0001t0028g0231 | 2 | HG01192.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1291-744C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835335 | ||||||
| chr16:87835342
|
G | A | 5 | a0002c0004t0019g0010a0002c0004t0019g0044a0002c0004t0043g0041others(2): Show | 5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291-751C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835342 | ||||||
| chr16:87835342
|
G | C | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(159): Show | 166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1291-751C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835342 | ||||||
| chr16:87835368
|
C | G | 155 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(152): Show | 156 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.1291-777G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835368 | ||||||
| chr16:87835373
|
C | T | 6 | a0001c0001t0014g0052a0001c0001t0014g0259a0001c0001t0014g0260others(3): Show | 6 | HG02622.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291-782G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835373 | ||||||
| chr16:87835484
|
A | T | 35 | a0001c0001t0002g0105a0001c0001t0002g0195a0001c0001t0004g0265others(32): Show | 35 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1291-893T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835484 | ||||||
| chr16:87835503
|
T | C | 1 | a0001c0001t0003g0358 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1291-912A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835503 | ||||||
| chr16:87835537
|
T | G | 1 | a0001c0001t0004g0124 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1291-946A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835537 | ||||||
| chr16:87835547
|
T | C | 6 | a0001c0001t0014g0052a0001c0001t0014g0259a0001c0001t0014g0260others(3): Show | 6 | HG02622.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1290+951A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835547 | ||||||
| chr16:87835566
|
C | T | 14 | a0001c0001t0012g0131a0001c0001t0020g0227a0001c0001t0026g0126others(11): Show | 14 | HG01081.hp2 HG01167.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1290+932G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835566 | ||||||
| chr16:87835574
|
T | C | 1 | a0001c0001t0002g0251 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1290+924A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835574 | ||||||
| chr16:87835614
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(322): Show | 330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.1290+884A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835614 | ||||||
| chr16:87835619
|
G | A | 2 | a0002c0004t0043g0041a0002c0004t0044g0043 | 2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1290+879C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835619 | ||||||
| chr16:87835623
|
G | A | 1 | a0001c0013t0012g0165 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1290+875C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835623 | ||||||
| chr16:87835633
|
C | G | 1 | a0001c0002t0016g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1290+865G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835633 | ||||||
| chr16:87835663
|
A | G | 2 | a0001c0001t0013g0154a0001c0002t0013g0008 | 2 | HG03831.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1290+835T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835663 | ||||||
| chr16:87835664
|
C | T | 26 | a0001c0001t0002g0105a0001c0001t0002g0195a0001c0001t0002g0248others(23): Show | 26 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1290+834G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835664 | ||||||
| chr16:87835676
|
G | A | 1 | a0001c0001t0006g0168 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1290+822C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835676 | ||||||
| chr16:87835690
|
G | A | 1 | a0001c0001t0006g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1290+808C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835690 | ||||||
| chr16:87835695
|
C | T | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1290+803G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835695 | ||||||
| chr16:87835696
|
T | A | 1 | a0001c0001t0002g0076 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1290+802A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835696 | ||||||
| chr16:87835696
|
T | G | 28 | a0001c0001t0003g0332a0001c0001t0003g0341a0001c0001t0005g0098others(25): Show | 29 | HG01167.hp1 HG01891.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1290+802A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835696 | ||||||
| chr16:87835707
|
T | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(162): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1290+791A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835707 | ||||||
| chr16:87835709
|
T | C | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1290+789A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835709 | ||||||
| chr16:87835716
|
T | C | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1290+782A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835716 | ||||||
| chr16:87835717
|
G | A | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1290+781C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835717 | ||||||
| chr16:87835721
|
G | T | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1290+777C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835721 | ||||||
| chr16:87835761
|
A | G | 13 | a0001c0001t0003g0354a0001c0001t0010g0267a0001c0001t0010g0288others(10): Show | 13 | HG00639.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1290+737T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835761 | ||||||
| chr16:87835763
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1290+735G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835763 | ||||||
| chr16:87835764
|
G | A | 14 | a0001c0001t0003g0354a0001c0001t0010g0267a0001c0001t0010g0288others(11): Show | 14 | HG00639.hp2 HG02630.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1290+734C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835764 | ||||||
| chr16:87835765
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1290+733G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835765 | ||||||
| chr16:87835767
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1290+731G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835767 | ||||||
| chr16:87835770
|
A | C | 3 | a0001c0001t0004g0178a0001c0001t0004g0179a0001c0001t0012g0268 | 3 | HG02015.hp2 NA18950.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1290+728T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835770 | ||||||
| chr16:87835770
|
A | G | 73 | a0001c0001t0001g0180a0001c0001t0001g0241a0001c0001t0001g0276others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1290+728T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835770 | ||||||
| chr16:87835788
|
C | T | 1 | a0001c0001t0004g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1290+710G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835788 | ||||||
| chr16:87835809
|
G | C | 1 | a0001c0001t0011g0337 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1290+689C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835809 | ||||||
| chr16:87835910
|
C | G | 79 | a0001c0001t0002g0105a0001c0001t0002g0195a0001c0001t0002g0248others(76): Show | 79 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.1290+588G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835910 | ||||||
| chr16:87835934
|
C | T | 48 | a0001c0001t0002g0105a0001c0001t0002g0195a0001c0001t0002g0248others(45): Show | 48 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1290+564G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835934 | ||||||
| chr16:87836034
|
G | A | 108 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(105): Show | 109 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.1290+464C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87836034 | ||||||
| chr16:87836105
|
C | T | 72 | a0001c0001t0002g0105a0001c0001t0002g0195a0001c0001t0002g0248others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1290+393G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87836105 | ||||||
| chr16:87836386
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1290+112C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87836386 | ||||||
| chr16:87836438
|
G | A | 1 | a0004c0014t0035g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1290+60C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87836438 | ||||||
| chr16:87836686
|
C | T | 14 | a0001c0001t0008g0144a0001c0001t0008g0145a0001c0001t0008g0146others(11): Show | 14 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1141-39G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836686 | ||||||
| chr16:87836703
|
G | A | 1 | a0007c0010t0001g0211 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1141-56C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836703 | ||||||
| chr16:87836706
|
C | T | 72 | a0001c0001t0002g0105a0001c0001t0002g0195a0001c0001t0002g0248others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1141-59G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836706 | ||||||
| chr16:87836740
|
G | A | 1 | a0004c0008t0064g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1141-93C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836740 | ||||||
| chr16:87836773
|
A | G | 72 | a0001c0001t0002g0105a0001c0001t0002g0195a0001c0001t0002g0248others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1141-126T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836773 | ||||||
| chr16:87836867
|
A | G | 1 | a0001c0002t0041g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1141-220T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836867 | ||||||
| chr16:87836948
|
T | C | 9 | a0001c0001t0001g0180a0001c0001t0006g0130a0001c0001t0006g0168others(6): Show | 9 | HG00733.hp2 HG02965.hp2 HG03654.hp2 others(6): Show |
intron_variant | MODIFIER | c.1141-301A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836948 | ||||||
| chr16:87836968
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1141-321G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836968 | ||||||
| chr16:87837001
|
A | G | 66 | a0001c0001t0002g0105a0001c0001t0002g0195a0001c0001t0002g0299others(63): Show | 66 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.1141-354T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837001 | ||||||
| chr16:87837045
|
C | T | 4 | a0001c0001t0065g0374a0004c0008t0064g0319a0004c0014t0035g0005others(1): Show | 4 | HG02451.hp1 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-398G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837045 | ||||||
| chr16:87837067
|
G | A | 44 | a0001c0001t0001g0296a0001c0001t0003g0330a0001c0001t0003g0332others(41): Show | 44 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.1141-420C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837067 | ||||||
| chr16:87837117
|
G | C | 88 | a0001c0001t0003g0330a0001c0001t0003g0332a0001c0001t0003g0336others(85): Show | 89 | HG00438.hp1 HG00639.hp2 HG01167.hp1 others(86): Show |
intron_variant | MODIFIER | c.1141-470C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837117 | ||||||
| chr16:87837204
|
T | G | 13 | a0001c0001t0008g0144a0001c0001t0008g0145a0001c0001t0008g0146others(10): Show | 13 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1141-557A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837204 | ||||||
| chr16:87837260
|
T | C | 317 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(314): Show | 322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1140+585A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837260 | ||||||
| chr16:87837297
|
T | TG | 74 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(71): Show | 74 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1140+547dupC | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837297 | ||||||
| chr16:87837321
|
C | G | 1 | a0001c0001t0034g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1140+524G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837321 | ||||||
| chr16:87837407
|
T | A | 5 | a0001c0001t0017g0055a0001c0001t0017g0109a0001c0001t0017g0120others(2): Show | 5 | HG03041.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140+438A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837407 | ||||||
| chr16:87837490
|
A | G | 74 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(71): Show | 74 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1140+355T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837490 | ||||||
| chr16:87837535
|
C | T | 3 | a0001c0001t0005g0150a0001c0001t0005g0152a0001c0001t0005g0153 | 3 | NA18959.hp1 NA18966.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1140+310G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837535 | ||||||
| chr16:87837550
|
C | G | 1 | a0001c0002t0001g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1140+295G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837550 | ||||||
| chr16:87837595
|
G | A | 6 | a0001c0001t0011g0377a0001c0001t0030g0311a0001c0001t0030g0312others(3): Show | 8 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1140+250C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837595 | ||||||
| chr16:87837607
|
G | A | 72 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+238C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837607 | ||||||
| chr16:87837622
|
G | A | 3 | a0001c0001t0005g0150a0001c0001t0005g0152a0001c0001t0005g0153 | 3 | NA18959.hp1 NA18966.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1140+223C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837622 | ||||||
| chr16:87837637
|
T | A | 1 | a0004c0014t0035g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1140+208A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837637 | ||||||
| chr16:87837658
|
A | G | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(309): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.1140+187T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837658 | ||||||
| chr16:87837734
|
C | T | 27 | a0001c0001t0006g0066a0001c0001t0006g0130a0001c0001t0008g0144others(24): Show | 28 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1140+111G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837734 | ||||||
| chr16:87837760
|
G | C | 72 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+85C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837760 | ||||||
| chr16:87837797
|
C | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0213a0001c0001t0001g0216others(1): Show | 4 | HG02027.hp2 HG02040.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140+48G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837797 | ||||||
| chr16:87837976
|
G | A | 71 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(68): Show | 71 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1044-35C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87837976 | ||||||
| chr16:87838022
|
G | C | 1 | a0001c0001t0062g0353 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1044-81C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838022 | ||||||
| chr16:87838108
|
T | G | 313 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(310): Show | 318 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.1044-167A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838108 | ||||||
| chr16:87838157
|
C | G | 2 | a0002c0004t0043g0041a0002c0004t0044g0043 | 2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1044-216G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838157 | ||||||
| chr16:87838215
|
C | G | 1 | a0001c0001t0073g0385 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1044-274G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838215 | ||||||
| chr16:87838291
|
C | CT | 72 | a0001c0001t0001g0300a0001c0001t0003g0330a0001c0001t0003g0332others(69): Show | 73 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(70): Show |
intron_variant | MODIFIER | c.1044-351dupA | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838291 | ||||||
| chr16:87838291
|
C | CTT | 6 | a0001c0001t0003g0366a0001c0001t0004g0264a0001c0001t0023g0352others(3): Show | 6 | HG00438.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044-352_1044-351d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838291 | ||||||
| chr16:87838291
|
CT | C | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(160): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1044-351delA | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838291 | ||||||
| chr16:87838291
|
CTTTTTT | C | 70 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(67): Show | 70 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.1044-356_1044-351d others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838291 | ||||||
| chr16:87838403
|
G | C | 73 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(70): Show | 73 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.1043+311C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838403 | ||||||
| chr16:87838433
|
G | A | 4 | a0001c0001t0003g0354a0001c0001t0024g0355a0001c0001t0024g0356others(1): Show | 4 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+281C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838433 | ||||||
| chr16:87838482
|
G | A | 4 | a0001c0001t0067g0324a0001c0002t0027g0016a0001c0002t0027g0017others(1): Show | 4 | HG02145.hp1 HG02965.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+232C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838482 | ||||||
| chr16:87838708
|
G | A | 13 | a0001c0001t0008g0144a0001c0001t0008g0145a0001c0001t0008g0146others(10): Show | 13 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1043+6C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838708 | ||||||
| chr16:87838882
|
G | A | 72 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.940-65C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87838882 | ||||||
| chr16:87839010
|
C | G | 1 | a0001c0001t0017g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.940-193G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839010 | ||||||
| chr16:87839057
|
T | A | 1 | a0001c0001t0034g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.940-240A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839057 | ||||||
| chr16:87839111
|
C | G | 2 | a0002c0004t0043g0041a0002c0004t0044g0043 | 2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.940-294G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839111 | ||||||
| chr16:87839112
|
G | C | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(324): Show | 332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.940-295C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839112 | ||||||
| chr16:87839136
|
C | T | 2 | a0002c0004t0043g0041a0002c0004t0044g0043 | 2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.940-319G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839136 | ||||||
| chr16:87839137
|
G | A | 41 | a0001c0001t0003g0330a0001c0001t0003g0332a0001c0001t0003g0336others(38): Show | 41 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.940-320C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839137 | ||||||
| chr16:87839147
|
C | T | 2 | a0001c0001t0005g0058a0001c0002t0005g0009 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.940-330G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839147 | ||||||
| chr16:87839238
|
A | G | 326 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(323): Show | 331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.940-421T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839238 | ||||||
| chr16:87839245
|
G | A | 7 | a0001c0001t0006g0066a0001c0001t0067g0324a0001c0002t0006g0002others(4): Show | 8 | HG02055.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.940-428C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839245 | ||||||
| chr16:87839250
|
C | A | 4 | a0001c0001t0006g0066a0001c0002t0006g0002a0001c0002t0006g0045others(1): Show | 5 | HG02055.hp2 HG02486.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-433G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839250 | ||||||
| chr16:87839338
|
C | T | 1 | a0001c0001t0009g0220 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.939+364G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839338 | ||||||
| chr16:87839430
|
G | A | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0011g0325 | 3 | HG00140.hp2 HG00738.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.939+272C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839430 | ||||||
| chr16:87839526
|
C | T | 51 | a0001c0001t0003g0330a0001c0001t0003g0332a0001c0001t0003g0336others(48): Show | 51 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.939+176G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839526 | ||||||
| chr16:87839584
|
G | A | 2 | a0002c0004t0043g0041a0002c0004t0044g0043 | 2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.939+118C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839584 | ||||||
| chr16:87839614
|
G | A | 1 | a0001c0001t0034g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.939+88C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839614 | ||||||
| chr16:87839641
|
A | C | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(215): Show | 222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.939+61T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839641 | ||||||
| chr16:87839830
|
A | G | 1 | a0001c0001t0011g0369 | 1 | NA19066.hp1 | splice_region_variant&intron_variant | LOW | c.816-5T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839830 | ||||||
| chr16:87839836
|
C | G | 3 | a0001c0001t0002g0192a0001c0001t0007g0327a0001c0001t0007g0328 | 3 | HG01106.hp1 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.816-11G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839836 | ||||||
| chr16:87839865
|
G | A | 41 | a0001c0001t0003g0330a0001c0001t0003g0332a0001c0001t0003g0336others(38): Show | 41 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.816-40C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839865 | ||||||
| chr16:87839914
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.816-89C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839914 | ||||||
| chr16:87839918
|
T | G | 1 | a0001c0002t0001g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.816-93A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839918 | ||||||
| chr16:87839971
|
A | G | 80 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(77): Show | 81 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.816-146T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839971 | ||||||
| chr16:87839983
|
G | C | 1 | a0001c0001t0004g0176 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.816-158C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839983 | ||||||
| chr16:87839991
|
G | C | 13 | a0001c0001t0008g0144a0001c0001t0008g0145a0001c0001t0008g0146others(10): Show | 13 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.816-166C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839991 | ||||||
| chr16:87840026
|
T | C | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.816-201A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87840026 | ||||||
| chr16:87840146
|
G | A | 3 | a0001c0001t0004g0178a0001c0001t0004g0179a0004c0008t0064g0319 | 3 | HG03579.hp1 NA18950.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.815+283C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87840146 | ||||||
| chr16:87840320
|
G | T | 1 | a0004c0008t0064g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.815+109C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87840320 | ||||||
| chr16:87840501
|
TATATG | T | 71 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(68): Show | 71 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.771-33_771-29delCA others(3): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840501 | ||||||
| chr16:87840534
|
G | A | 40 | a0001c0001t0003g0330a0001c0001t0003g0332a0001c0001t0003g0336others(37): Show | 40 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.771-61C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840534 | ||||||
| chr16:87840576
|
T | C | 71 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(68): Show | 71 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.771-103A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840576 | ||||||
| chr16:87840600
|
C | T | 8 | a0001c0001t0001g0180a0001c0001t0006g0168a0001c0001t0006g0177others(5): Show | 8 | HG00733.hp2 HG03654.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.771-127G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840600 | ||||||
| chr16:87840611
|
TGGGA | T | 71 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(68): Show | 71 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.771-142_771-139del others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840611 | ||||||
| chr16:87840633
|
C | T | 2 | a0004c0008t0064g0319a0004c0014t0035g0005 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.771-160G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840633 | ||||||
| chr16:87840640
|
C | T | 10 | a0001c0001t0006g0128a0001c0001t0006g0129a0001c0001t0006g0164others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.771-167G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840640 | ||||||
| chr16:87840723
|
G | A | 1 | a0001c0001t0016g0285 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.771-250C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840723 | ||||||
| chr16:87840730
|
G | A | 71 | a0001c0001t0001g0180a0001c0001t0002g0105a0001c0001t0002g0195others(68): Show | 71 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.771-257C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840730 | ||||||
| chr16:87840786
|
C | T | 2 | a0001c0002t0027g0016a0001c0002t0027g0017 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.770+264G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840786 | ||||||
| chr16:87840787
|
G | A | 1 | a0001c0001t0004g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.770+263C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840787 | ||||||
| chr16:87840817
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0003g0357 | 2 | HG01243.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.770+233C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840817 | ||||||
| chr16:87840820
|
G | A | 39 | a0001c0001t0003g0330a0001c0001t0003g0332a0001c0001t0003g0336others(36): Show | 39 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.770+230C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840820 | ||||||
| chr16:87840907
|
TCTTTAAC others(37): Show |
T | 2 | a0001c0001t0006g0130a0001c0001t0034g0006 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.770+99_770+142delG others(43): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840907 | ||||||
| chr16:87840943
|
G | A | 1 | a0001c0001t0070g0368 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.770+107C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840943 | ||||||
| chr16:87841250
|
A | G | 10 | a0001c0001t0006g0066a0001c0002t0006g0002a0001c0002t0006g0045others(7): Show | 11 | HG02055.hp2 HG02486.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.665-95T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841250 | ||||||
| chr16:87841292
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.665-137C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841292 | ||||||
| chr16:87841347
|
A | G | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665-192T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841347 | ||||||
| chr16:87841502
|
G | A | 1 | a0001c0001t0018g0316 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.665-347C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841502 | ||||||
| chr16:87841557
|
C | A | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665-402G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841557 | ||||||
| chr16:87841558
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.665-403C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841558 | ||||||
| chr16:87841623
|
C | T | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665-468G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841623 | ||||||
| chr16:87841678
|
T | C | 20 | a0001c0001t0006g0128a0001c0001t0006g0129a0001c0001t0014g0052others(17): Show | 20 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.665-523A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841678 | ||||||
| chr16:87841794
|
C | T | 1 | a0001c0001t0009g0104 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.665-639G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841794 | ||||||
| chr16:87841797
|
G | A | 2 | a0001c0001t0002g0249a0001c0001t0002g0251 | 2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.665-642C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841797 | ||||||
| chr16:87841893
|
T | C | 2 | a0001c0001t0003g0354a0004c0008t0064g0319 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.665-738A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841893 | ||||||
| chr16:87842102
|
AAAG | A | 3 | a0001c0001t0013g0282a0001c0001t0032g0347a0001c0001t0032g0348 | 3 | HG00323.hp2 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.665-950_665-948del others(3): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842102 | ||||||
| chr16:87842272
|
C | T | 1 | a0004c0014t0035g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.665-1117G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842272 | ||||||
| chr16:87842312
|
G | T | 1 | a0001c0001t0003g0366 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-1157C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842312 | ||||||
| chr16:87842313
|
T | G | 1 | a0001c0001t0003g0366 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-1158A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842313 | ||||||
| chr16:87842324
|
G | A | 1 | a0001c0002t0020g0028 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665-1169C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842324 | ||||||
| chr16:87842403
|
G | A | 1 | a0001c0001t0003g0339 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.665-1248C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842403 | ||||||
| chr16:87842520
|
C | A | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0276others(5): Show | 8 | HG00140.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.665-1365G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842520 | ||||||
| chr16:87842558
|
T | C | 22 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(19): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.665-1403A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842558 | ||||||
| chr16:87842569
|
C | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(152): Show | 159 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.665-1414G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842569 | ||||||
| chr16:87842666
|
G | C | 2 | a0001c0001t0029g0161a0001c0001t0029g0162 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.665-1511C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842666 | ||||||
| chr16:87842696
|
C | T | 1 | a0004c0008t0064g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.665-1541G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842696 | ||||||
| chr16:87842769
|
T | C | 142 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(139): Show | 142 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.665-1614A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842769 | ||||||
| chr16:87842777
|
CCAGGTGG others(4): Show |
C | 1 | a0001c0002t0010g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.665-1633_665-1623d others(13): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842777 | ||||||
| chr16:87842868
|
G | A | 1 | a0001c0001t0004g0117 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.665-1713C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842868 | ||||||
| chr16:87842869
|
G | GCCAAGAC others(3): Show |
318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(315): Show | 323 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.665-1715_665-1714i others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842869 | ||||||
| chr16:87842869
|
G | GCCAAGAT others(3): Show |
1 | a0004c0014t0035g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.665-1715_665-1714i others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842869 | ||||||
| chr16:87842894
|
A | G | 125 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(122): Show | 125 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.665-1739T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842894 | ||||||
| chr16:87842935
|
C | T | 3 | a0001c0001t0022g0170a0001c0001t0022g0183a0001c0001t0022g0184 | 3 | HG00735.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.665-1780G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842935 | ||||||
| chr16:87842961
|
C | T | 135 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(132): Show | 135 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.665-1806G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842961 | ||||||
| chr16:87843025
|
C | A | 136 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(133): Show | 136 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.665-1870G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843025 | ||||||
| chr16:87843109
|
G | A | 1 | a0001c0001t0003g0366 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-1954C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843109 | ||||||
| chr16:87843206
|
T | C | 137 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(134): Show | 137 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.665-2051A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843206 | ||||||
| chr16:87843214
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.665-2059T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843214 | ||||||
| chr16:87843226
|
G | C | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665-2071C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843226 | ||||||
| chr16:87843253
|
T | C | 324 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(321): Show | 329 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.665-2098A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843253 | ||||||
| chr16:87843292
|
T | C | 1 | a0001c0002t0041g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.665-2137A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843292 | ||||||
| chr16:87843347
|
C | CT | 11 | a0001c0001t0001g0068a0001c0001t0001g0276a0001c0001t0001g0277others(8): Show | 11 | HG00140.hp2 HG00738.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.665-2193dupA | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CT | C | 7 | a0001c0001t0002g0142a0001c0001t0002g0192a0001c0001t0002g0200others(4): Show | 7 | HG01070.hp1 HG01106.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.665-2193delA | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CTTTTTTT | C | 18 | a0001c0001t0006g0066a0001c0001t0006g0129a0001c0001t0014g0052others(15): Show | 19 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.665-2199_665-2193d others(9): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CTTTTTTT others(1): Show |
C | 26 | a0001c0001t0001g0004a0001c0001t0001g0138a0001c0001t0001g0151others(23): Show | 27 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.665-2200_665-2193d others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CTTTTTTT others(2): Show |
C | 108 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0065others(105): Show | 111 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.665-2201_665-2193d others(11): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CTTTTTTT others(3): Show |
C | 20 | a0001c0001t0001g0158a0001c0001t0001g0234a0001c0001t0001g0245others(17): Show | 20 | HG00323.hp1 HG00408.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.665-2202_665-2193d others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0006g0130a0001c0001t0033g0360 | 2 | HG02965.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.665-2203_665-2193d others(13): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CTTTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0069a0001c0001t0003g0367a0001c0001t0003g0371others(5): Show | 8 | HG01346.hp1 HG02109.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.665-2204_665-2193d others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CTTTTTTT others(6): Show |
C | 41 | a0001c0001t0001g0266a0001c0001t0003g0330a0001c0001t0003g0332others(38): Show | 41 | HG00438.hp1 HG00639.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.665-2205_665-2193d others(15): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CTTTTTTT others(7): Show |
C | 74 | a0001c0001t0001g0180a0001c0001t0001g0270a0001c0001t0002g0074others(71): Show | 74 | HG00423.hp2 HG00642.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.665-2206_665-2193d others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CTTTTTTT others(8): Show |
C | 14 | a0001c0001t0002g0105a0001c0001t0003g0366a0001c0001t0008g0145others(11): Show | 14 | HG00323.hp2 HG01123.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.665-2207_665-2193d others(17): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0008g0144a0001c0002t0008g0037 | 2 | HG01167.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.665-2208_665-2193d others(18): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CTTTTTTT others(15): Show |
C | 5 | a0001c0001t0001g0073a0001c0001t0003g0341a0001c0001t0003g0346others(2): Show | 5 | HG00438.hp2 HG02683.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.665-2214_665-2193d others(24): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843347
|
CTTTTTTT others(16): Show |
C | 1 | a0001c0011t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.665-2215_665-2193d others(25): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | ||||||
| chr16:87843407
|
T | C | 136 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(133): Show | 136 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.665-2252A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843407 | ||||||
| chr16:87843494
|
C | T | 137 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(134): Show | 137 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.665-2339G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843494 | ||||||
| chr16:87843591
|
C | T | 1 | a0001c0001t0034g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.665-2436G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843591 | ||||||
| chr16:87843613
|
G | A | 3 | a0001c0001t0005g0079a0001c0001t0005g0101a0001c0001t0013g0155 | 3 | HG01361.hp1 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.665-2458C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843613 | ||||||
| chr16:87843640
|
T | C | 138 | a0001c0001t0001g0180a0001c0001t0001g0198a0001c0001t0001g0266others(135): Show | 138 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.665-2485A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843640 | ||||||
| chr16:87843695
|
G | A | 1 | a0001c0011t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.665-2540C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843695 | ||||||
| chr16:87843706
|
G | A | 137 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(134): Show | 137 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.665-2551C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843706 | ||||||
| chr16:87843707
|
C | G | 137 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(134): Show | 137 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.665-2552G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843707 | ||||||
| chr16:87843766
|
G | A | 1 | a0001c0001t0025g0334 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.665-2611C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843766 | ||||||
| chr16:87843962
|
G | C | 2 | a0004c0014t0035g0005a0004c0015t0042g0056 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.665-2807C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843962 | ||||||
| chr16:87844152
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.665-2997T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844152 | ||||||
| chr16:87844155
|
G | A | 1 | a0001c0001t0011g0375 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.665-3000C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844155 | ||||||
| chr16:87844258
|
G | A | 1 | a0001c0001t0002g0196 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.665-3103C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844258 | ||||||
| chr16:87844289
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.665-3134C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844289 | ||||||
| chr16:87844297
|
C | T | 1 | a0001c0001t0034g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.665-3142G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844297 | ||||||
| chr16:87844298
|
G | A | 2 | a0001c0001t0007g0331a0001c0001t0053g0091 | 2 | NA18983.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.665-3143C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844298 | ||||||
| chr16:87844309
|
C | G | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-3154G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844309 | ||||||
| chr16:87844317
|
C | T | 12 | a0001c0001t0006g0130a0001c0001t0006g0164a0001c0001t0017g0055others(9): Show | 12 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.665-3162G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844317 | ||||||
| chr16:87844323
|
T | C | 14 | a0001c0001t0006g0130a0001c0001t0006g0164a0001c0001t0017g0055others(11): Show | 14 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.665-3168A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844323 | ||||||
| chr16:87844333
|
G | A | 2 | a0001c0001t0005g0058a0001c0002t0005g0009 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.665-3178C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844333 | ||||||
| chr16:87844346
|
G | A | 14 | a0001c0001t0006g0130a0001c0001t0006g0164a0001c0001t0017g0055others(11): Show | 14 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.665-3191C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844346 | ||||||
| chr16:87844358
|
C | T | 1 | a0001c0001t0024g0355 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.665-3203G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844358 | ||||||
| chr16:87844424
|
C | T | 1 | a0003c0006t0014g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.665-3269G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844424 | ||||||
| chr16:87844456
|
G | A | 1 | a0001c0001t0003g0366 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-3301C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844456 | ||||||
| chr16:87844466
|
C | A | 143 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(140): Show | 143 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.665-3311G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844466 | ||||||
| chr16:87844470
|
G | A | 143 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(140): Show | 143 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.665-3315C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844470 | ||||||
| chr16:87844527
|
C | T | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665-3372G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844527 | ||||||
| chr16:87844556
|
T | G | 143 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(140): Show | 143 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.665-3401A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844556 | ||||||
| chr16:87844559
|
T | C | 143 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(140): Show | 143 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.665-3404A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844559 | ||||||
| chr16:87844560
|
G | T | 2 | a0001c0001t0003g0362a0001c0001t0003g0364 | 2 | HG03688.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.665-3405C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844560 | ||||||
| chr16:87844613
|
T | G | 39 | a0001c0001t0003g0330a0001c0001t0003g0332a0001c0001t0003g0336others(36): Show | 39 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.665-3458A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844613 | ||||||
| chr16:87844618
|
G | A | 1 | a0001c0001t0005g0148 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.665-3463C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844618 | ||||||
| chr16:87844662
|
G | A | 38 | a0001c0001t0003g0330a0001c0001t0003g0332a0001c0001t0003g0336others(35): Show | 38 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.665-3507C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844662 | ||||||
| chr16:87844662
|
G | C | 1 | a0004c0014t0035g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.665-3507C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844662 | ||||||
| chr16:87844760
|
G | A | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-3605C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844760 | ||||||
| chr16:87844767
|
T | G | 1 | a0001c0002t0041g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.665-3612A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844767 | ||||||
| chr16:87844788
|
C | T | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-3633G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844788 | ||||||
| chr16:87844793
|
TCCAACCA others(8): Show |
T | 2 | a0001c0001t0004g0121a0001c0001t0004g0214 | 2 | NA18954.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.665-3653_665-3639d others(17): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844793 | ||||||
| chr16:87844870
|
G | A | 142 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(139): Show | 142 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.665-3715C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844870 | ||||||
| chr16:87844907
|
G | A | 1 | a0001c0002t0008g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.665-3752C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844907 | ||||||
| chr16:87844964
|
G | A | 129 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(126): Show | 129 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.665-3809C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844964 | ||||||
| chr16:87845045
|
C | A | 129 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(126): Show | 129 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.665-3890G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845045 | ||||||
| chr16:87845081
|
G | C | 2 | a0001c0001t0029g0161a0001c0001t0029g0162 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.665-3926C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845081 | ||||||
| chr16:87845102
|
A | G | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(317): Show | 325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.665-3947T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845102 | ||||||
| chr16:87845177
|
C | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(152): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.665-4022G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845177 | ||||||
| chr16:87845181
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.665-4026C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845181 | ||||||
| chr16:87845193
|
C | CT | 143 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(140): Show | 143 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.665-4039_665-4038i others(3): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845193 | ||||||
| chr16:87845216
|
G | A | 143 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(140): Show | 143 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.665-4061C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845216 | ||||||
| chr16:87845235
|
G | A | 1 | a0001c0001t0069g0323 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.665-4080C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845235 | ||||||
| chr16:87845277
|
C | G | 142 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(139): Show | 142 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.665-4122G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845277 | ||||||
| chr16:87845343
|
C | T | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-4188G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845343 | ||||||
| chr16:87845356
|
G | T | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665-4201C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845356 | ||||||
| chr16:87845358
|
A | G | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(320): Show | 328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.665-4203T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845358 | ||||||
| chr16:87845362
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0059g0173 | 2 | NA18986.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.665-4207C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845362 | ||||||
| chr16:87845404
|
G | C | 2 | a0001c0002t0027g0016a0001c0002t0027g0017 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.665-4249C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845404 | ||||||
| chr16:87845411
|
T | TGCCCACC others(13): Show |
1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-4276_665-4257d others(22): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845411 | ||||||
| chr16:87845472
|
G | A | 1 | a0001c0002t0001g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.665-4317C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845472 | ||||||
| chr16:87845478
|
C | G | 1 | a0001c0001t0046g0122 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.665-4323G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845478 | ||||||
| chr16:87845491
|
C | T | 1 | a0001c0001t0006g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.665-4336G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845491 | ||||||
| chr16:87845509
|
T | TGCCCACC others(53): Show |
1 | a0001c0001t0003g0363 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.665-4355_665-4354i others(62): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845509 | ||||||
| chr16:87845510
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.665-4355C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845510 | ||||||
| chr16:87845516
|
T | C | 1 | a0001c0001t0003g0363 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.665-4361A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845516 | ||||||
| chr16:87845516
|
T | TCCAGGCA others(135): Show |
1 | a0001c0001t0034g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.665-4362_665-4361i others(144): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845516 | ||||||
| chr16:87845516
|
T | TCCAGGCA others(75): Show |
140 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(137): Show | 140 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.665-4362_665-4361i others(84): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845516 | ||||||
| chr16:87845531
|
C | T | 1 | a0001c0001t0003g0366 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-4376G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845531 | ||||||
| chr16:87845543
|
G | A | 1 | a0001c0001t0003g0366 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-4388C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845543 | ||||||
| chr16:87845552
|
G | A | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-4397C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845552 | ||||||
| chr16:87845557
|
C | CCCCAGAG others(76): Show |
1 | a0001c0001t0003g0366 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-4403_665-4402i others(85): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845557 | ||||||
| chr16:87845557
|
C | T | 141 | a0001c0001t0001g0180a0001c0001t0001g0266a0001c0001t0001g0270others(138): Show | 141 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.665-4402G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845557 | ||||||
| chr16:87845643
|
T | A | 1 | a0001c0001t0003g0366 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-4488A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845643 | ||||||
| chr16:87845695
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.665-4540C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845695 | ||||||
| chr16:87845753
|
C | G | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-4598G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845753 | ||||||
| chr16:87845786
|
G | A | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(170): Show | 178 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.665-4631C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845786 | ||||||
| chr16:87845798
|
T | G | 1 | a0001c0002t0001g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.665-4643A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845798 | ||||||
| chr16:87845823
|
G | C | 1 | a0001c0001t0004g0214 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.665-4668C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845823 | ||||||
| chr16:87845849
|
G | A | 1 | a0004c0008t0064g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.665-4694C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845849 | ||||||
| chr16:87845880
|
G | A | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(170): Show | 178 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.665-4725C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845880 | ||||||
| chr16:87845916
|
G | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(176): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.665-4761C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845916 | ||||||
| chr16:87845927
|
C | T | 6 | a0001c0001t0014g0052a0001c0001t0014g0259a0001c0001t0014g0260others(3): Show | 6 | HG02622.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.665-4772G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845927 | ||||||
| chr16:87845956
|
C | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(176): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.665-4801G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845956 | ||||||
| chr16:87845970
|
G | A | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665-4815C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845970 | ||||||
| chr16:87846060
|
T | G | 23 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(20): Show | 24 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.665-4905A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846060 | ||||||
| chr16:87846119
|
C | T | 2 | a0001c0001t0065g0374a0004c0015t0042g0056 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.665-4964G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846119 | ||||||
| chr16:87846138
|
GGCCCAGG others(14): Show |
G | 1 | a0001c0001t0004g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.665-5004_665-4984d others(23): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846138 | ||||||
| chr16:87846163
|
A | G | 25 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(22): Show | 26 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.665-5008T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846163 | ||||||
| chr16:87846210
|
G | C | 1 | a0004c0008t0064g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.665-5055C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846210 | ||||||
| chr16:87846233
|
A | C | 23 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(20): Show | 24 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.665-5078T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846233 | ||||||
| chr16:87846259
|
T | C | 23 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(20): Show | 24 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.665-5104A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846259 | ||||||
| chr16:87846362
|
C | A | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665-5207G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846362 | ||||||
| chr16:87846405
|
G | A | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665-5250C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846405 | ||||||
| chr16:87846454
|
C | T | 5 | a0002c0004t0019g0010a0002c0004t0019g0044a0002c0004t0043g0041others(2): Show | 5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+5270G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846454 | ||||||
| chr16:87846483
|
G | A | 15 | a0001c0001t0006g0128a0001c0001t0006g0129a0001c0001t0014g0052others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.664+5241C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846483 | ||||||
| chr16:87846609
|
A | G | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+5115T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846609 | ||||||
| chr16:87846624
|
G | T | 1 | a0001c0002t0008g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.664+5100C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846624 | ||||||
| chr16:87846660
|
C | G | 1 | a0001c0001t0014g0052 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.664+5064G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846660 | ||||||
| chr16:87846779
|
C | T | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+4945G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846779 | ||||||
| chr16:87846797
|
C | T | 1 | a0001c0001t0005g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.664+4927G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846797 | ||||||
| chr16:87846814
|
A | G | 23 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(20): Show | 24 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.664+4910T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846814 | ||||||
| chr16:87846855
|
G | A | 1 | a0001c0001t0070g0368 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.664+4869C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846855 | ||||||
| chr16:87846879
|
C | T | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.664+4845G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846879 | ||||||
| chr16:87846964
|
C | T | 1 | a0001c0002t0005g0049 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.664+4760G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846964 | ||||||
| chr16:87846975
|
G | C | 1 | a0001c0001t0003g0378 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.664+4749C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846975 | ||||||
| chr16:87847063
|
C | T | 40 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(37): Show | 40 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.664+4661G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847063 | ||||||
| chr16:87847096
|
C | T | 11 | a0001c0001t0006g0164a0001c0001t0017g0055a0001c0001t0017g0109others(8): Show | 11 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.664+4628G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847096 | ||||||
| chr16:87847097
|
G | A | 1 | a0004c0014t0035g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.664+4627C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847097 | ||||||
| chr16:87847186
|
C | T | 11 | a0001c0001t0006g0164a0001c0001t0017g0055a0001c0001t0017g0109others(8): Show | 11 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.664+4538G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847186 | ||||||
| chr16:87847286
|
T | C | 5 | a0002c0004t0019g0010a0002c0004t0019g0044a0002c0004t0043g0041others(2): Show | 5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+4438A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847286 | ||||||
| chr16:87847307
|
G | A | 1 | a0001c0001t0013g0167 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.664+4417C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847307 | ||||||
| chr16:87847325
|
G | A | 1 | a0001c0002t0066g0320 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.664+4399C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847325 | ||||||
| chr16:87847340
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.664+4384C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847340 | ||||||
| chr16:87847361
|
A | G | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(180): Show | 188 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.664+4363T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847361 | ||||||
| chr16:87847368
|
G | C | 1 | a0001c0002t0041g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.664+4356C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847368 | ||||||
| chr16:87847387
|
AGCCAGAT others(4): Show |
A | 6 | a0001c0001t0001g0095a0001c0001t0001g0213a0001c0001t0001g0216others(3): Show | 6 | HG00673.hp1 HG02027.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.664+4326_664+4336d others(13): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847387 | ||||||
| chr16:87847414
|
C | T | 10 | a0001c0001t0001g0180a0001c0001t0001g0270a0001c0001t0006g0130others(7): Show | 10 | HG00733.hp2 HG02965.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.664+4310G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847414 | ||||||
| chr16:87847523
|
C | T | 1 | a0001c0002t0020g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.664+4201G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847523 | ||||||
| chr16:87847587
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG00140.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.664+4137C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847587 | ||||||
| chr16:87847608
|
G | C | 5 | a0002c0004t0019g0010a0002c0004t0019g0044a0002c0004t0043g0041others(2): Show | 5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+4116C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847608 | ||||||
| chr16:87847682
|
C | G | 1 | a0001c0002t0001g0013 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.664+4042G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847682 | ||||||
| chr16:87847683
|
C | T | 2 | a0001c0002t0006g0045a0001c0002t0039g0047 | 2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.664+4041G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847683 | ||||||
| chr16:87847684
|
A | G | 23 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(20): Show | 24 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.664+4040T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847684 | ||||||
| chr16:87847689
|
C | T | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+4035G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847689 | ||||||
| chr16:87847709
|
A | G | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+4015T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847709 | ||||||
| chr16:87847759
|
G | C | 4 | a0001c0001t0006g0164a0001c0001t0026g0126a0001c0001t0040g0163others(1): Show | 4 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+3965C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847759 | ||||||
| chr16:87847777
|
C | T | 26 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(23): Show | 27 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.664+3947G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847777 | ||||||
| chr16:87847828
|
A | G | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+3896T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847828 | ||||||
| chr16:87847850
|
A | G | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664+3874T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847850 | ||||||
| chr16:87847868
|
G | A | 4 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(1): Show | 4 | HG00099.hp1 HG00323.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+3856C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847868 | ||||||
| chr16:87847961
|
C | A | 1 | a0004c0014t0035g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.664+3763G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847961 | ||||||
| chr16:87847979
|
G | A | 2 | a0001c0001t0007g0331a0001c0001t0053g0091 | 2 | NA18983.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.664+3745C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847979 | ||||||
| chr16:87848021
|
G | A | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+3703C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848021 | ||||||
| chr16:87848124
|
G | C | 13 | a0001c0001t0008g0144a0001c0001t0008g0145a0001c0001t0008g0146others(10): Show | 13 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.664+3600C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848124 | ||||||
| chr16:87848139
|
T | TC | 159 | a0001c0001t0001g0180a0001c0001t0001g0270a0001c0001t0002g0084others(156): Show | 160 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.664+3584_664+3585i others(3): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848139 | ||||||
| chr16:87848238
|
A | G | 2 | a0001c0001t0067g0324a0004c0014t0035g0005 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.664+3486T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848238 | ||||||
| chr16:87848282
|
C | T | 1 | a0001c0001t0011g0369 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.664+3442G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848282 | ||||||
| chr16:87848438
|
C | A | 2 | a0001c0001t0003g0371a0001c0001t0003g0372 | 2 | HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.664+3286G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848438 | ||||||
| chr16:87848480
|
G | A | 1 | a0001c0001t0005g0166 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.664+3244C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848480 | ||||||
| chr16:87848518
|
T | C | 175 | a0001c0001t0001g0180a0001c0001t0001g0270a0001c0001t0002g0084others(172): Show | 176 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.664+3206A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848518 | ||||||
| chr16:87848528
|
T | C | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.664+3196A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848528 | ||||||
| chr16:87848562
|
G | C | 2 | a0001c0002t0020g0028a0001c0002t0020g0029 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.664+3162C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848562 | ||||||
| chr16:87848603
|
A | G | 174 | a0001c0001t0001g0180a0001c0001t0001g0270a0001c0001t0002g0084others(171): Show | 175 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.664+3121T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848603 | ||||||
| chr16:87848691
|
A | G | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+3033T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848691 | ||||||
| chr16:87848729
|
C | T | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+2995G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848729 | ||||||
| chr16:87848773
|
C | G | 1 | a0001c0001t0030g0312 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.664+2951G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848773 | ||||||
| chr16:87848824
|
C | T | 22 | a0001c0001t0002g0067a0001c0001t0006g0066a0001c0001t0006g0128others(19): Show | 23 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.664+2900G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848824 | ||||||
| chr16:87848827
|
C | G | 5 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0276others(2): Show | 5 | HG00140.hp2 HG00738.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+2897G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848827 | ||||||
| chr16:87848829
|
T | C | 3 | a0001c0001t0002g0087a0001c0001t0002g0200a0001c0001t0009g0088 | 3 | HG00544.hp2 NA18988.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.664+2895A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848829 | ||||||
| chr16:87848835
|
C | T | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+2889G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848835 | ||||||
| chr16:87848876
|
G | T | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664+2848C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848876 | ||||||
| chr16:87848890
|
CA | C | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+2833delT | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848890 | ||||||
| chr16:87848903
|
C | T | 169 | a0001c0001t0001g0180a0001c0001t0001g0270a0001c0001t0002g0084others(166): Show | 170 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.664+2821G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848903 | ||||||
| chr16:87848915
|
A | AGGCAAGA others(8): Show |
169 | a0001c0001t0001g0180a0001c0001t0001g0270a0001c0001t0002g0084others(166): Show | 170 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.664+2808_664+2809i others(17): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848915 | ||||||
| chr16:87848933
|
A | G | 169 | a0001c0001t0001g0180a0001c0001t0001g0270a0001c0001t0002g0084others(166): Show | 170 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.664+2791T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848933 | ||||||
| chr16:87848964
|
C | G | 1 | a0004c0008t0064g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.664+2760G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848964 | ||||||
| chr16:87849037
|
C | A | 1 | a0001c0001t0068g0379 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.664+2687G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849037 | ||||||
| chr16:87849089
|
C | A | 154 | a0001c0001t0001g0180a0001c0001t0001g0270a0001c0001t0002g0084others(151): Show | 154 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.664+2635G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849089 | ||||||
| chr16:87849223
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.664+2501G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849223 | ||||||
| chr16:87849230
|
TG | T | 167 | a0001c0001t0001g0180a0001c0001t0001g0270a0001c0001t0002g0084others(164): Show | 168 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.664+2493delC | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849230 | ||||||
| chr16:87849234
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.664+2490C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849234 | ||||||
| chr16:87849451
|
T | C | 19 | a0001c0001t0001g0053a0001c0001t0001g0149a0001c0001t0001g0159others(16): Show | 19 | HG00438.hp2 HG00597.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.664+2273A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849451 | ||||||
| chr16:87849483
|
C | T | 107 | a0001c0001t0001g0180a0001c0001t0001g0270a0001c0001t0002g0084others(104): Show | 107 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.664+2241G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849483 | ||||||
| chr16:87849536
|
C | G | 1 | a0001c0001t0001g0229 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.664+2188G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849536 | ||||||
| chr16:87849553
|
G | A | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+2171C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849553 | ||||||
| chr16:87849592
|
C | T | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.664+2132G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849592 | ||||||
| chr16:87849638
|
A | G | 1 | a0001c0002t0041g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.664+2086T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849638 | ||||||
| chr16:87849645
|
C | T | 5 | a0001c0001t0065g0374a0001c0002t0001g0035a0001c0002t0041g0036others(2): Show | 5 | HG02451.hp1 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+2079G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849645 | ||||||
| chr16:87849657
|
A | G | 5 | a0001c0001t0003g0365a0001c0001t0003g0366a0001c0001t0003g0367others(2): Show | 5 | NA18939.hp2 NA18963.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+2067T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849657 | ||||||
| chr16:87849712
|
G | C | 1 | a0001c0001t0060g0141 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.664+2012C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849712 | ||||||
| chr16:87849853
|
A | T | 1 | a0001c0001t0030g0312 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.664+1871T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849853 | ||||||
| chr16:87849861
|
G | A | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.664+1863C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849861 | ||||||
| chr16:87850115
|
A | C | 332 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(329): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.664+1609T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850115 | ||||||
| chr16:87850127
|
G | A | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664+1597C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850127 | ||||||
| chr16:87850129
|
C | T | 1 | a0001c0001t0013g0282 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.664+1595G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850129 | ||||||
| chr16:87850130
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.664+1594C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850130 | ||||||
| chr16:87850139
|
C | G | 1 | a0001c0001t0054g0094 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.664+1585G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850139 | ||||||
| chr16:87850213
|
G | T | 2 | a0001c0001t0065g0374a0004c0015t0042g0056 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.664+1511C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850213 | ||||||
| chr16:87850236
|
C | T | 1 | a0001c0001t0071g0340 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.664+1488G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850236 | ||||||
| chr16:87850312
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0159 | 2 | NA18960.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.664+1412C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850312 | ||||||
| chr16:87850335
|
C | T | 1 | a0001c0002t0045g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.664+1389G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850335 | ||||||
| chr16:87850383
|
T | C | 2 | a0001c0001t0067g0324a0004c0014t0035g0005 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.664+1341A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850383 | ||||||
| chr16:87850391
|
G | A | 2 | a0001c0001t0004g0114a0001c0001t0011g0337 | 2 | HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.664+1333C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850391 | ||||||
| chr16:87850502
|
G | A | 1 | a0001c0001t0015g0160 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.664+1222C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850502 | ||||||
| chr16:87850503
|
A | G | 1 | a0001c0001t0015g0160 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.664+1221T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850503 | ||||||
| chr16:87850729
|
A | T | 1 | a0001c0001t0015g0160 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.664+995T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850729 | ||||||
| chr16:87850734
|
T | C | 3 | a0001c0001t0065g0374a0001c0002t0041g0036a0004c0015t0042g0056 | 3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.664+990A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850734 | ||||||
| chr16:87850735
|
G | A | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.664+989C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850735 | ||||||
| chr16:87850758
|
T | C | 3 | a0001c0001t0065g0374a0001c0002t0041g0036a0004c0015t0042g0056 | 3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.664+966A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850758 | ||||||
| chr16:87850765
|
G | A | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+959C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850765 | ||||||
| chr16:87850839
|
A | G | 1 | a0001c0002t0001g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.664+885T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850839 | ||||||
| chr16:87850873
|
G | C | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.664+851C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850873 | ||||||
| chr16:87850941
|
A | G | 153 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0180others(150): Show | 153 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.664+783T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850941 | ||||||
| chr16:87851092
|
A | G | 1 | a0001c0001t0024g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.664+632T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851092 | ||||||
| chr16:87851156
|
G | GTCTGAGT others(27): Show |
6 | a0001c0001t0015g0062a0001c0001t0015g0063a0001c0001t0015g0064others(3): Show | 6 | NA18948.hp1 NA18964.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.664+534_664+567dup others(34): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851156 | ||||||
| chr16:87851192
|
C | T | 3 | a0001c0001t0065g0374a0001c0002t0041g0036a0004c0015t0042g0056 | 3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.664+532G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851192 | ||||||
| chr16:87851289
|
G | A | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.664+435C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851289 | ||||||
| chr16:87851295
|
C | T | 2 | a0001c0001t0020g0227a0001c0002t0020g0029 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.664+429G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851295 | ||||||
| chr16:87851308
|
G | A | 3 | a0001c0001t0065g0374a0001c0002t0041g0036a0004c0015t0042g0056 | 3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.664+416C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851308 | ||||||
| chr16:87851359
|
T | G | 3 | a0001c0001t0065g0374a0001c0002t0041g0036a0004c0015t0042g0056 | 3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.664+365A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851359 | ||||||
| chr16:87851446
|
G | A | 2 | a0001c0001t0020g0227a0001c0002t0020g0029 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.664+278C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851446 | ||||||
| chr16:87851663
|
G | A | 1 | a0001c0001t0068g0379 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.664+61C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851663 | ||||||
| chr16:87851696
|
G | A | 5 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250others(2): Show | 5 | HG00738.hp1 HG01978.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+28C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851696 | ||||||
| chr16:87851867
|
A | G | 3 | a0001c0001t0065g0374a0001c0002t0041g0036a0004c0015t0042g0056 | 3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.539-18T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87851867 | ||||||
| chr16:87851936
|
C | A | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539-87G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87851936 | ||||||
| chr16:87851999
|
T | C | 2 | a0001c0001t0006g0130a0004c0008t0064g0319 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.539-150A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87851999 | ||||||
| chr16:87852006
|
C | G | 4 | a0001c0001t0065g0374a0001c0002t0001g0035a0001c0002t0041g0036others(1): Show | 4 | HG02451.hp1 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.539-157G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852006 | ||||||
| chr16:87852007
|
G | A | 1 | a0001c0001t0067g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.539-158C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852007 | ||||||
| chr16:87852110
|
C | G | 1 | a0001c0001t0002g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.539-261G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852110 | ||||||
| chr16:87852129
|
T | C | 7 | a0001c0001t0065g0374a0001c0001t0067g0324a0001c0002t0001g0035others(4): Show | 7 | HG02451.hp1 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.539-280A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852129 | ||||||
| chr16:87852163
|
G | A | 1 | a0001c0001t0009g0104 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.539-314C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852163 | ||||||
| chr16:87852357
|
C | T | 5 | a0002c0004t0019g0010a0002c0004t0019g0044a0002c0004t0043g0041others(2): Show | 5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-508G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852357 | ||||||
| chr16:87852365
|
C | T | 1 | a0001c0001t0014g0259 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.539-516G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852365 | ||||||
| chr16:87852366
|
G | A | 3 | a0001c0001t0002g0083a0001c0001t0067g0324a0004c0014t0035g0005 | 3 | HG02965.hp1 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.539-517C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852366 | ||||||
| chr16:87852393
|
C | T | 5 | a0002c0004t0019g0010a0002c0004t0019g0044a0002c0004t0043g0041others(2): Show | 5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-544G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852393 | ||||||
| chr16:87852423
|
T | C | 1 | a0004c0008t0064g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.539-574A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852423 | ||||||
| chr16:87852427
|
G | A | 12 | a0001c0001t0006g0066a0001c0001t0014g0052a0001c0001t0014g0259others(9): Show | 13 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.539-578C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852427 | ||||||
| chr16:87852429
|
G | A | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-580C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852429 | ||||||
| chr16:87852435
|
C | A | 1 | a0001c0002t0016g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.539-586G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852435 | ||||||
| chr16:87852531
|
A | G | 3 | a0001c0001t0065g0374a0001c0002t0041g0036a0004c0015t0042g0056 | 3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.539-682T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852531 | ||||||
| chr16:87852557
|
T | C | 178 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0180others(175): Show | 179 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.539-708A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852557 | ||||||
| chr16:87852636
|
C | CCTCTGTC others(9): Show |
1 | a0001c0001t0004g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-788_539-787ins others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852636 | ||||||
| chr16:87852636
|
CTCTGTGT others(5): Show |
C | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539-799_539-788del others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852636 | ||||||
| chr16:87852638
|
C | CTG | 28 | a0001c0001t0001g0071a0001c0001t0001g0093a0001c0001t0001g0138others(25): Show | 28 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.539-791_539-790dup others(2): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
C | CTGTG | 22 | a0001c0001t0001g0198a0001c0001t0001g0232a0001c0001t0001g0258others(19): Show | 22 | HG00544.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.539-793_539-790dup others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
C | CTGTGTG | 26 | a0001c0001t0001g0151a0001c0001t0001g0174a0001c0001t0001g0235others(23): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.539-795_539-790dup others(6): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
C | CTGTGTGT others(1): Show |
19 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0065others(16): Show | 21 | HG00423.hp1 HG00621.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.539-797_539-790dup others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
C | CTGTGTGT others(3): Show |
32 | a0001c0001t0001g0053a0001c0001t0001g0140a0001c0001t0001g0157others(29): Show | 32 | HG00140.hp1 HG00438.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.539-799_539-790dup others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
C | CTGTGTGT others(5): Show |
41 | a0001c0001t0001g0072a0001c0001t0001g0103a0001c0001t0001g0107others(38): Show | 41 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.539-801_539-790dup others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
C | CTGTGTGT others(7): Show |
24 | a0001c0001t0001g0095a0001c0001t0001g0113a0001c0001t0001g0119others(21): Show | 24 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.539-803_539-790dup others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0028g0231 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.539-805_539-790dup others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
C | CTGTGTGT others(11): Show |
2 | a0001c0001t0001g0111a0001c0001t0001g0139 | 2 | NA19085.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.539-807_539-790dup others(18): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
C | G | 2 | a0001c0001t0004g0108a0004c0015t0042g0056 | 2 | HG02451.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.539-789G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
CTG | C | 33 | a0001c0001t0001g0118a0001c0001t0001g0277a0001c0001t0002g0074others(30): Show | 34 | HG00140.hp2 HG00558.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.539-791_539-790del others(2): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
CTGTG | C | 29 | a0001c0001t0001g0270a0001c0001t0002g0190a0001c0001t0002g0280others(26): Show | 29 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.539-793_539-790del others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
CTGTGTG | C | 46 | a0001c0001t0001g0082a0001c0001t0001g0180a0001c0001t0001g0266others(43): Show | 46 | HG00438.hp1 HG00733.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.539-795_539-790del others(6): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
CTGTGTGT others(1): Show |
C | 4 | a0001c0001t0005g0058a0001c0001t0017g0055a0001c0001t0017g0120others(1): Show | 4 | HG02258.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.539-797_539-790del others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
CTGTGTGT others(3): Show |
C | 6 | a0001c0001t0006g0164a0001c0001t0017g0109a0001c0001t0017g0208others(3): Show | 6 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.539-799_539-790del others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0005g0166 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.539-801_539-790del others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0002g0279 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.539-803_539-790del others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852638
|
CTGTGTGT others(15): Show |
C | 1 | a0001c0002t0055g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.539-811_539-790del others(22): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | ||||||
| chr16:87852641
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0011g0377 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.539-793_539-792ins others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852641 | ||||||
| chr16:87852643
|
T | TGTGTGTG others(5): Show |
3 | a0001c0001t0030g0311a0001c0001t0030g0312a0001c0002t0001g0001 | 5 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-795_539-794ins others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852643 | ||||||
| chr16:87852657
|
T | C | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-808A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852657 | ||||||
| chr16:87852665
|
T | A | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-816A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852665 | ||||||
| chr16:87852669
|
TGTGTGTG others(8): Show |
T | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-835_539-821del others(15): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852669 | ||||||
| chr16:87852686
|
G | T | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-837C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852686 | ||||||
| chr16:87852687
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0300 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.539-839_539-838ins others(11): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852687 | ||||||
| chr16:87852687
|
T | TGTGTGTG others(6): Show |
1 | a0001c0001t0001g0242 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.539-839_539-838ins others(13): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852687 | ||||||
| chr16:87852688
|
T | G | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-839A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852688 | ||||||
| chr16:87852689
|
G | T | 1 | a0001c0001t0001g0300 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.539-840C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852689 | ||||||
| chr16:87852708
|
A | G | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-859T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852708 | ||||||
| chr16:87852736
|
T | C | 5 | a0002c0004t0019g0010a0002c0004t0019g0044a0002c0004t0043g0041others(2): Show | 5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-887A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852736 | ||||||
| chr16:87852742
|
T | C | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-893A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852742 | ||||||
| chr16:87852770
|
C | T | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-921G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852770 | ||||||
| chr16:87852772
|
A | T | 1 | a0001c0001t0072g0384 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.539-923T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852772 | ||||||
| chr16:87852778
|
G | A | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-929C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852778 | ||||||
| chr16:87852779
|
C | G | 178 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0180others(175): Show | 179 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.539-930G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852779 | ||||||
| chr16:87852780
|
G | A | 1 | a0001c0001t0033g0380 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.539-931C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852780 | ||||||
| chr16:87852830
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.539-981G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852830 | ||||||
| chr16:87852833
|
C | T | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539-984G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852833 | ||||||
| chr16:87852884
|
C | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(139): Show | 146 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.539-1035G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852884 | ||||||
| chr16:87852933
|
G | C | 3 | a0001c0001t0020g0227a0001c0002t0020g0028a0001c0002t0020g0029 | 3 | HG02258.hp2 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.539-1084C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852933 | ||||||
| chr16:87852934
|
G | A | 20 | a0001c0001t0002g0075a0001c0001t0002g0077a0001c0001t0002g0087others(17): Show | 20 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.539-1085C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852934 | ||||||
| chr16:87852939
|
C | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(167): Show | 175 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.539-1090G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852939 | ||||||
| chr16:87852944
|
G | A | 4 | a0001c0001t0006g0271a0001c0001t0022g0170a0001c0001t0022g0183others(1): Show | 4 | HG00735.hp2 HG01433.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-1095C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852944 | ||||||
| chr16:87852947
|
G | A | 1 | a0001c0001t0006g0271 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.539-1098C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852947 | ||||||
| chr16:87853020
|
A | G | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.539-1171T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853020 | ||||||
| chr16:87853040
|
C | G | 1 | a0001c0001t0006g0271 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.539-1191G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853040 | ||||||
| chr16:87853043
|
T | C | 1 | a0001c0001t0004g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-1194A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853043 | ||||||
| chr16:87853044
|
C | T | 1 | a0001c0001t0004g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-1195G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853044 | ||||||
| chr16:87853053
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.539-1204C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853053 | ||||||
| chr16:87853094
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.539-1245G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853094 | ||||||
| chr16:87853095
|
G | A | 1 | a0001c0002t0045g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.539-1246C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853095 | ||||||
| chr16:87853105
|
CTT | C | 21 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(18): Show | 22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.539-1258_539-1257d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853105 | ||||||
| chr16:87853120
|
T | A | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(141): Show | 148 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.539-1271A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853120 | ||||||
| chr16:87853123
|
G | T | 1 | a0004c0014t0035g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.539-1274C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853123 | ||||||
| chr16:87853130
|
C | T | 2 | a0001c0001t0009g0169a0001c0001t0009g0293 | 2 | NA18980.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.539-1281G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853130 | ||||||
| chr16:87853132
|
C | T | 1 | a0001c0001t0004g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-1283G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853132 | ||||||
| chr16:87853228
|
C | T | 22 | a0001c0001t0006g0066a0001c0001t0006g0128a0001c0001t0006g0129others(19): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.539-1379G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853228 | ||||||
| chr16:87853266
|
G | A | 1 | a0001c0001t0003g0330 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.539-1417C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853266 | ||||||
| chr16:87853296
|
C | T | 1 | a0001c0001t0005g0166 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.539-1447G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853296 | ||||||
| chr16:87853300
|
T | C | 1 | a0001c0002t0010g0011 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.539-1451A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853300 | ||||||
| chr16:87853328
|
G | A | 3 | a0001c0002t0026g0014a0001c0002t0027g0016a0001c0002t0027g0017 | 3 | HG02145.hp1 HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.539-1479C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853328 | ||||||
| chr16:87853443
|
A | G | 12 | a0001c0001t0002g0087a0001c0001t0002g0089a0001c0001t0002g0133others(9): Show | 12 | HG00544.hp2 HG02129.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.539-1594T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853443 | ||||||
| chr16:87853498
|
C | G | 1 | a0001c0001t0017g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539-1649G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853498 | ||||||
| chr16:87853595
|
T | C | 132 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0180others(129): Show | 132 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.539-1746A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853595 | ||||||
| chr16:87853601
|
G | A | 1 | a0001c0002t0041g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.539-1752C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853601 | ||||||
| chr16:87853656
|
G | C | 1 | a0001c0001t0001g0095 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.539-1807C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853656 | ||||||
| chr16:87853701
|
G | A | 5 | a0001c0001t0001g0107a0001c0001t0001g0138a0001c0001t0004g0114others(2): Show | 5 | HG01978.hp1 HG02293.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-1852C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853701 | ||||||
| chr16:87853712
|
A | AGCTTTCT others(1): Show |
17 | a0001c0001t0001g0053a0001c0001t0001g0149a0001c0001t0001g0159others(14): Show | 17 | HG00438.hp2 HG00597.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.539-1871_539-1864d others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853712 | ||||||
| chr16:87853713
|
G | T | 1 | a0001c0001t0004g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-1864C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853713 | ||||||
| chr16:87853734
|
C | T | 1 | a0004c0008t0064g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.539-1885G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853734 | ||||||
| chr16:87853735
|
C | T | 1 | a0001c0001t0054g0094 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.539-1886G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853735 | ||||||
| chr16:87853752
|
C | T | 1 | a0001c0001t0012g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.539-1903G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853752 | ||||||
| chr16:87853781
|
A | G | 5 | a0001c0001t0013g0167a0001c0001t0018g0313a0001c0001t0018g0314others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-1932T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853781 | ||||||
| chr16:87853805
|
G | A | 1 | a0001c0001t0017g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539-1956C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853805 | ||||||
| chr16:87853825
|
G | C | 2 | a0001c0002t0006g0002a0001c0002t0010g0046 | 3 | HG02486.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.539-1976C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853825 | ||||||
| chr16:87853836
|
A | C | 1 | a0001c0001t0011g0325 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.539-1987T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853836 | ||||||
| chr16:87853837
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.539-1988G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853837 | ||||||
| chr16:87853845
|
C | A | 11 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0243others(8): Show | 11 | HG01123.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.539-1996G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853845 | ||||||
| chr16:87853877
|
G | C | 330 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(327): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.539-2028C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853877 | ||||||
| chr16:87853885
|
T | C | 1 | a0001c0001t0067g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.539-2036A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853885 | ||||||
| chr16:87853890
|
A | G | 16 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0276others(13): Show | 16 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.539-2041T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853890 | ||||||
| chr16:87853898
|
CGCGGCTG others(8): Show |
C | 39 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0197others(36): Show | 39 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.539-2064_539-2050d others(17): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853898 | ||||||
| chr16:87853915
|
C | T | 3 | a0001c0002t0008g0042a0002c0004t0019g0044a0002c0004t0044g0043 | 3 | HG02630.hp2 HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.539-2066G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853915 | ||||||
| chr16:87853924
|
C | T | 1 | a0001c0002t0002g0012 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.539-2075G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853924 | ||||||
| chr16:87853936
|
G | A | 6 | a0001c0001t0002g0089a0001c0001t0002g0171a0001c0001t0002g0181others(3): Show | 6 | HG02129.hp2 NA18947.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.539-2087C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853936 | ||||||
| chr16:87853939
|
TG | T | 19 | a0001c0001t0002g0299a0001c0001t0006g0130a0001c0001t0006g0164others(16): Show | 19 | HG01167.hp2 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.539-2091delC | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853939 | ||||||
| chr16:87853954
|
G | A | 78 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0219others(75): Show | 80 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.539-2105C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853954 | ||||||
| chr16:87853960
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.539-2111G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853960 | ||||||
| chr16:87853994
|
C | T | 1 | a0001c0001t0006g0129 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.539-2145G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853994 | ||||||
| chr16:87854072
|
G | C | 10 | a0001c0001t0001g0139a0001c0001t0001g0270a0001c0001t0002g0083others(7): Show | 10 | HG00642.hp2 HG01109.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.539-2223C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | ||||||
| chr16:87854072
|
G | GC | 123 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0111others(120): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.539-2224dupG | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | ||||||
| chr16:87854072
|
G | GCC | 56 | a0001c0001t0001g0093a0001c0001t0001g0127a0001c0001t0001g0151others(53): Show | 56 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.539-2225_539-2224d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | ||||||
| chr16:87854072
|
G | GCCC | 23 | a0001c0001t0001g0069a0001c0001t0002g0085a0001c0001t0002g0251others(20): Show | 23 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.539-2226_539-2224d others(5): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | ||||||
| chr16:87854072
|
G | GCCCC | 31 | a0001c0001t0001g0174a0001c0001t0001g0266a0001c0001t0002g0084others(28): Show | 31 | HG00280.hp2 HG00597.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.539-2227_539-2224d others(6): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | ||||||
| chr16:87854072
|
GC | G | 41 | a0001c0001t0001g0072a0001c0001t0001g0107a0001c0001t0001g0194others(38): Show | 41 | HG00642.hp1 HG01081.hp2 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.539-2224delG | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | ||||||
| chr16:87854072
|
GCC | G | 58 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0082others(55): Show | 59 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.539-2225_539-2224d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | ||||||
| chr16:87854074
|
C | G | 1 | a0007c0010t0001g0211 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.539-2225G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854074 | ||||||
| chr16:87854108
|
C | A | 1 | a0001c0001t0067g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.539-2259G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854108 | ||||||
| chr16:87854111
|
T | A | 52 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0277others(49): Show | 52 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.539-2262A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854111 | ||||||
| chr16:87854114
|
C | T | 25 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0119others(22): Show | 25 | HG00558.hp2 HG00673.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.539-2265G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854114 | ||||||
| chr16:87854142
|
G | T | 203 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0068others(200): Show | 207 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.539-2293C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854142 | ||||||
| chr16:87854145
|
T | C | 206 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0068others(203): Show | 210 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.539-2296A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854145 | ||||||
| chr16:87854158
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.539-2309C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854158 | ||||||
| chr16:87854194
|
A | G | 4 | a0001c0001t0001g0207a0001c0001t0002g0075a0001c0001t0002g0077others(1): Show | 4 | HG02056.hp2 NA18940.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-2345T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854194 | ||||||
| chr16:87854200
|
G | A | 73 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0119others(70): Show | 73 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.539-2351C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854200 | ||||||
| chr16:87854281
|
T | C | 1 | a0001c0001t0062g0353 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.539-2432A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854281 | ||||||
| chr16:87854350
|
A | G | 2 | a0001c0002t0010g0011a0002c0004t0019g0010 | 2 | HG00639.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.539-2501T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854350 | ||||||
| chr16:87854352
|
G | C | 1 | a0001c0001t0013g0275 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.539-2503C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854352 | ||||||
| chr16:87854438
|
A | G | 29 | a0001c0001t0004g0283a0001c0001t0006g0164a0001c0001t0010g0267others(26): Show | 29 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.539-2589T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854438 | ||||||
| chr16:87854462
|
G | A | 4 | a0001c0002t0008g0042a0002c0004t0019g0044a0002c0004t0043g0041others(1): Show | 4 | HG02630.hp2 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-2613C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854462 | ||||||
| chr16:87854482
|
C | A | 60 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0180others(57): Show | 62 | HG00323.hp2 HG00642.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.539-2633G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854482 | ||||||
| chr16:87854513
|
T | C | 273 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(270): Show | 277 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.539-2664A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854513 | ||||||
| chr16:87854550
|
G | T | 1 | a0004c0008t0064g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.539-2701C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854550 | ||||||
| chr16:87854597
|
T | A | 1 | a0001c0002t0041g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.539-2748A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854597 | ||||||
| chr16:87854632
|
G | A | 1 | a0001c0001t0067g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.539-2783C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854632 | ||||||
| chr16:87854633
|
C | T | 1 | a0001c0001t0004g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-2784G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854633 | ||||||
| chr16:87854635
|
A | C | 1 | a0001c0001t0004g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-2786T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854635 | ||||||
| chr16:87854636
|
C | A | 1 | a0001c0001t0004g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-2787G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854636 | ||||||
| chr16:87854657
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.539-2808C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854657 | ||||||
| chr16:87854696
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.539-2847C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854696 | ||||||
| chr16:87854698
|
C | G | 1 | a0001c0001t0004g0117 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.539-2849G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854698 | ||||||
| chr16:87854707
|
C | A | 1 | a0001c0001t0004g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-2858G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854707 | ||||||
| chr16:87854711
|
G | A | 8 | a0001c0001t0010g0267a0001c0001t0010g0288a0001c0002t0008g0037others(5): Show | 8 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.539-2862C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854711 | ||||||
| chr16:87854716
|
G | A | 5 | a0001c0001t0004g0283a0001c0001t0018g0313a0001c0001t0018g0314others(2): Show | 5 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-2867C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854716 | ||||||
| chr16:87854954
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.539-3105C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854954 | ||||||
| chr16:87854984
|
C | T | 3 | a0001c0001t0005g0058a0001c0001t0012g0059a0001c0001t0012g0060 | 3 | HG01109.hp1 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.539-3135G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854984 | ||||||
| chr16:87855012
|
C | G | 1 | a0001c0001t0002g0196 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.539-3163G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855012 | ||||||
| chr16:87855127
|
T | C | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(274): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.539-3278A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855127 | ||||||
| chr16:87855130
|
G | A | 260 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(257): Show | 262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.539-3281C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855130 | ||||||
| chr16:87855137
|
G | A | 3 | a0001c0001t0034g0006a0001c0002t0001g0035a0004c0014t0035g0005 | 3 | HG02723.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.539-3288C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855137 | ||||||
| chr16:87855549
|
C | T | 260 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(257): Show | 262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.539-3700G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855549 | ||||||
| chr16:87855554
|
T | C | 260 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(257): Show | 262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.539-3705A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855554 | ||||||
| chr16:87855597
|
G | A | 224 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(221): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.539-3748C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855597 | ||||||
| chr16:87855806
|
C | T | 259 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(256): Show | 261 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.539-3957G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855806 | ||||||
| chr16:87855887
|
C | T | 256 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(253): Show | 258 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.539-4038G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855887 | ||||||
| chr16:87855889
|
T | C | 259 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(256): Show | 261 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.539-4040A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855889 | ||||||
| chr16:87855954
|
G | A | 1 | a0001c0001t0023g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.539-4105C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855954 | ||||||
| chr16:87855956
|
C | T | 71 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0004g0283others(68): Show | 74 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.539-4107G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855956 | ||||||
| chr16:87855959
|
C | T | 41 | a0001c0001t0001g0065a0001c0001t0001g0157a0001c0001t0001g0266others(38): Show | 41 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.539-4110G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855959 | ||||||
| chr16:87855962
|
T | C | 4 | a0001c0002t0006g0024a0001c0002t0006g0025a0001c0002t0006g0026others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-4113A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855962 | ||||||
| chr16:87856020
|
CCTGTCTG others(12): Show |
C | 1 | a0001c0001t0047g0210 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.539-4190_539-4172d others(21): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856020 | ||||||
| chr16:87856040
|
C | T | 28 | a0001c0001t0005g0166a0001c0001t0006g0066a0001c0001t0007g0327others(25): Show | 30 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.539-4191G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856040 | ||||||
| chr16:87856108
|
C | T | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(211): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.539-4259G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856108 | ||||||
| chr16:87856234
|
G | A | 41 | a0001c0001t0001g0082a0001c0001t0001g0157a0001c0001t0001g0266others(38): Show | 41 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.539-4385C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856234 | ||||||
| chr16:87856236
|
G | A | 4 | a0001c0002t0026g0014a0001c0002t0027g0016a0001c0002t0027g0017others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-4387C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856236 | ||||||
| chr16:87856254
|
T | C | 260 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(257): Show | 262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.539-4405A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856254 | ||||||
| chr16:87856358
|
G | A | 1 | a0001c0013t0012g0165 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.539-4509C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856358 | ||||||
| chr16:87856439
|
A | G | 4 | a0001c0001t0020g0227a0001c0001t0065g0374a0001c0002t0012g0050others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-4590T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856439 | ||||||
| chr16:87856463
|
C | T | 1 | a0001c0001t0020g0227 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.539-4614G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856463 | ||||||
| chr16:87856512
|
C | A | 13 | a0001c0001t0001g0180a0001c0001t0001g0269a0001c0001t0001g0270others(10): Show | 13 | HG00673.hp1 HG00733.hp2 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.539-4663G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856512 | ||||||
| chr16:87856646
|
G | A | 1 | a0001c0002t0010g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.539-4797C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856646 | ||||||
| chr16:87856661
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.539-4812G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856661 | ||||||
| chr16:87856824
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.539-4975G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856824 | ||||||
| chr16:87856835
|
A | G | 110 | a0001c0001t0001g0082a0001c0001t0001g0157a0001c0001t0001g0266others(107): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.539-4986T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856835 | ||||||
| chr16:87856849
|
G | T | 49 | a0001c0001t0004g0283a0001c0001t0005g0166a0001c0001t0006g0164others(46): Show | 50 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.539-5000C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856849 | ||||||
| chr16:87856893
|
G | A | 1 | a0001c0002t0041g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.539-5044C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856893 | ||||||
| chr16:87856966
|
C | T | 3 | a0001c0001t0004g0108a0001c0001t0004g0178a0001c0001t0004g0179 | 3 | NA18950.hp1 NA19060.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.539-5117G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856966 | ||||||
| chr16:87857008
|
C | CT | 110 | a0001c0001t0001g0082a0001c0001t0001g0157a0001c0001t0001g0266others(107): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.539-5160_539-5159i others(3): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857008 | ||||||
| chr16:87857096
|
C | T | 2 | a0001c0001t0017g0055a0001c0001t0017g0120 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.539-5247G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857096 | ||||||
| chr16:87857136
|
C | T | 32 | a0001c0001t0001g0082a0001c0001t0001g0157a0001c0001t0001g0266others(29): Show | 32 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.539-5287G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857136 | ||||||
| chr16:87857225
|
AT | A | 69 | a0001c0001t0004g0283a0001c0001t0005g0166a0001c0001t0006g0066others(66): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.539-5377delA | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857225 | ||||||
| chr16:87857308
|
C | T | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0012g0268 | 3 | HG00673.hp1 HG02015.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.539-5459G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857308 | ||||||
| chr16:87857365
|
G | A | 1 | a0001c0001t0030g0312 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.539-5516C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857365 | ||||||
| chr16:87857455
|
G | A | 64 | a0001c0001t0004g0283a0001c0001t0005g0166a0001c0001t0006g0066others(61): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.539-5606C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857455 | ||||||
| chr16:87857531
|
C | T | 4 | a0001c0002t0008g0042a0002c0004t0019g0044a0002c0004t0043g0041others(1): Show | 4 | HG02630.hp2 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-5682G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857531 | ||||||
| chr16:87857541
|
C | A | 8 | a0001c0001t0020g0227a0001c0002t0006g0023a0001c0002t0006g0024others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.539-5692G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857541 | ||||||
| chr16:87857563
|
G | A | 10 | a0001c0001t0010g0267a0001c0001t0010g0288a0001c0001t0073g0385others(7): Show | 10 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.539-5714C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857563 | ||||||
| chr16:87857584
|
G | A | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG01433.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.539-5735C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857584 | ||||||
| chr16:87857679
|
A | G | 64 | a0001c0001t0004g0283a0001c0001t0005g0166a0001c0001t0006g0066others(61): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.539-5830T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857679 | ||||||
| chr16:87857702
|
T | G | 5 | a0001c0001t0067g0324a0001c0002t0005g0009a0001c0002t0010g0011others(2): Show | 5 | HG00639.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-5853A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857702 | ||||||
| chr16:87857738
|
C | G | 31 | a0001c0001t0001g0157a0001c0001t0001g0266a0001c0001t0001g0290others(28): Show | 31 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.539-5889G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857738 | ||||||
| chr16:87857816
|
T | G | 4 | a0001c0001t0001g0266a0001c0001t0003g0338a0001c0001t0004g0264others(1): Show | 4 | HG00438.hp1 HG01993.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-5967A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857816 | ||||||
| chr16:87857905
|
G | A | 69 | a0001c0001t0004g0283a0001c0001t0005g0166a0001c0001t0006g0066others(66): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.539-6056C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857905 | ||||||
| chr16:87857907
|
G | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0179 | 2 | NA18950.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.539-6058C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857907 | ||||||
| chr16:87858152
|
T | G | 1 | a0001c0001t0021g0253 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.539-6303A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858152 | ||||||
| chr16:87858269
|
G | A | 108 | a0001c0001t0001g0082a0001c0001t0001g0157a0001c0001t0001g0266others(105): Show | 111 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.539-6420C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858269 | ||||||
| chr16:87858286
|
A | G | 37 | a0001c0001t0001g0082a0001c0001t0001g0157a0001c0001t0001g0266others(34): Show | 37 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.539-6437T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858286 | ||||||
| chr16:87858308
|
G | A | 3 | a0001c0001t0005g0058a0001c0001t0012g0059a0001c0001t0012g0060 | 3 | HG01109.hp1 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.539-6459C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858308 | ||||||
| chr16:87858416
|
C | T | 3 | a0001c0001t0005g0058a0001c0001t0012g0059a0001c0001t0012g0060 | 3 | HG01109.hp1 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.539-6567G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858416 | ||||||
| chr16:87858418
|
G | A | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(260): Show | 265 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.539-6569C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858418 | ||||||
| chr16:87858431
|
C | T | 1 | a0001c0001t0025g0334 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.539-6582G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858431 | ||||||
| chr16:87858570
|
C | T | 1 | a0001c0001t0036g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.539-6721G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858570 | ||||||
| chr16:87858598
|
T | A | 10 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0243others(7): Show | 10 | HG01123.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.539-6749A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858598 | ||||||
| chr16:87858665
|
T | C | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(324): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.539-6816A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858665 | ||||||
| chr16:87858696
|
C | T | 11 | a0001c0001t0004g0283a0001c0001t0006g0164a0001c0001t0018g0313others(8): Show | 11 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.539-6847G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858696 | ||||||
| chr16:87858698
|
G | A | 1 | a0001c0001t0003g0336 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.539-6849C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858698 | ||||||
| chr16:87858723
|
C | T | 2 | a0001c0001t0007g0327a0001c0001t0007g0328 | 2 | NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.539-6874G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858723 | ||||||
| chr16:87858798
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.539-6949C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858798 | ||||||
| chr16:87858813
|
C | T | 37 | a0001c0001t0001g0082a0001c0001t0001g0157a0001c0001t0001g0266others(34): Show | 37 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.539-6964G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858813 | ||||||
| chr16:87858848
|
G | A | 2 | a0001c0001t0034g0006a0001c0002t0001g0035 | 2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.539-6999C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858848 | ||||||
| chr16:87858885
|
C | A | 5 | a0001c0001t0067g0324a0001c0002t0005g0009a0001c0002t0010g0011others(2): Show | 5 | HG00639.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-7036G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858885 | ||||||
| chr16:87858970
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0060g0141 | 2 | HG01074.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.539-7121C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858970 | ||||||
| chr16:87859091
|
T | C | 1 | a0001c0001t0012g0268 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.539-7242A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859091 | ||||||
| chr16:87859196
|
G | A | 3 | a0001c0001t0013g0282a0001c0001t0032g0347a0001c0001t0032g0348 | 3 | HG00323.hp2 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.539-7347C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859196 | ||||||
| chr16:87859197
|
G | A | 1 | a0001c0001t0072g0384 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.539-7348C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859197 | ||||||
| chr16:87859248
|
G | C | 5 | a0001c0001t0006g0164a0001c0001t0040g0163a0001c0005t0031g0381others(2): Show | 5 | HG01081.hp2 HG02109.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-7399C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859248 | ||||||
| chr16:87859405
|
C | G | 66 | a0001c0001t0001g0082a0001c0001t0001g0157a0001c0001t0001g0266others(63): Show | 68 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.539-7556G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859405 | ||||||
| chr16:87859418
|
G | A | 1 | a0001c0003t0001g0102 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.539-7569C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859418 | ||||||
| chr16:87859504
|
G | A | 11 | a0001c0001t0004g0283a0001c0001t0006g0164a0001c0001t0018g0313others(8): Show | 11 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.539-7655C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859504 | ||||||
| chr16:87859552
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.539-7703G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859552 | ||||||
| chr16:87859576
|
G | A | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-7727C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859576 | ||||||
| chr16:87859754
|
C | T | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539-7905G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859754 | ||||||
| chr16:87859770
|
C | T | 1 | a0001c0001t0011g0337 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.539-7921G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859770 | ||||||
| chr16:87859803
|
T | G | 1 | a0001c0001t0023g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.539-7954A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859803 | ||||||
| chr16:87859913
|
A | AAAAAC | 32 | a0001c0001t0002g0105a0001c0001t0002g0192a0001c0001t0002g0195others(29): Show | 33 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.539-8069_539-8065d others(7): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859913 | ||||||
| chr16:87859913
|
AAAAAC | A | 38 | a0001c0001t0005g0166a0001c0001t0006g0066a0001c0001t0007g0327others(35): Show | 40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.539-8069_539-8065d others(7): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859913 | ||||||
| chr16:87860145
|
C | A | 42 | a0001c0001t0004g0283a0001c0001t0005g0058a0001c0001t0006g0164others(39): Show | 43 | HG00280.hp2 HG00639.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.539-8296G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860145 | ||||||
| chr16:87860265
|
G | A | 1 | a0001c0002t0016g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.539-8416C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860265 | ||||||
| chr16:87860323
|
C | A | 10 | a0001c0001t0010g0267a0001c0001t0010g0288a0001c0001t0073g0385others(7): Show | 10 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.539-8474G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860323 | ||||||
| chr16:87860325
|
CA | C | 8 | a0001c0001t0067g0324a0001c0002t0005g0009a0001c0002t0006g0025others(5): Show | 8 | HG00639.hp2 HG01884.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.539-8477delT | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860325 | ||||||
| chr16:87860337
|
A | T | 34 | a0001c0001t0001g0157a0001c0001t0001g0266a0001c0001t0001g0290others(31): Show | 34 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.539-8488T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860337 | ||||||
| chr16:87860337
|
AAAATACA others(7): Show |
A | 2 | a0001c0001t0073g0385a0001c0002t0045g0033 | 2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.539-8502_539-8489d others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860337 | ||||||
| chr16:87860338
|
AAATACAC others(4): Show |
A | 5 | a0001c0001t0002g0182a0001c0001t0008g0298a0001c0002t0001g0035others(2): Show | 5 | HG00099.hp2 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-8500_539-8490d others(13): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860338 | ||||||
| chr16:87860338
|
AAATACAC others(6): Show |
A | 3 | a0001c0001t0007g0327a0001c0001t0007g0328a0001c0002t0008g0042 | 3 | NA19043.hp1 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.539-8502_539-8490d others(15): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860338 | ||||||
| chr16:87860338
|
AAATACAC others(8): Show |
A | 11 | a0001c0001t0006g0066a0001c0001t0008g0145a0001c0002t0001g0001others(8): Show | 13 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.539-8504_539-8490d others(17): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860338 | ||||||
| chr16:87860339
|
A | T | 48 | a0001c0001t0001g0157a0001c0001t0001g0266a0001c0001t0001g0290others(45): Show | 48 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.539-8490T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860339 | ||||||
| chr16:87860341
|
T | TAC | 3 | a0001c0001t0001g0180a0001c0001t0002g0147a0001c0002t0066g0320 | 3 | HG01192.hp1 HG03669.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.539-8494_539-8493d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | ||||||
| chr16:87860341
|
T | TACAC | 4 | a0001c0001t0006g0130a0001c0001t0006g0177a0001c0001t0009g0088others(1): Show | 4 | HG01167.hp2 HG02965.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-8496_539-8493d others(6): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | ||||||
| chr16:87860341
|
TAC | T | 19 | a0001c0001t0002g0074a0001c0001t0002g0077a0001c0001t0002g0085others(16): Show | 19 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.539-8494_539-8493d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | ||||||
| chr16:87860341
|
TACAC | T | 14 | a0001c0001t0001g0065a0001c0001t0002g0084a0001c0001t0002g0105others(11): Show | 14 | HG00280.hp1 HG01123.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.539-8496_539-8493d others(6): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | ||||||
| chr16:87860341
|
TACACAC | T | 35 | a0001c0001t0001g0069a0001c0001t0001g0095a0001c0001t0001g0194others(32): Show | 35 | HG00597.hp2 HG01192.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.539-8498_539-8493d others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | ||||||
| chr16:87860341
|
TACACACA others(1): Show |
T | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0071others(59): Show | 64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.539-8500_539-8493d others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | ||||||
| chr16:87860341
|
TACACACA others(3): Show |
T | 84 | a0001c0001t0001g0053a0001c0001t0001g0072a0001c0001t0001g0082others(81): Show | 84 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.539-8502_539-8493d others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | ||||||
| chr16:87860341
|
TACACACA others(5): Show |
T | 31 | a0001c0001t0001g0068a0001c0001t0001g0103a0001c0001t0001g0107others(28): Show | 31 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.539-8504_539-8493d others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | ||||||
| chr16:87860341
|
TACACACA others(7): Show |
T | 13 | a0001c0001t0001g0113a0001c0001t0001g0138a0001c0001t0001g0139others(10): Show | 13 | HG01106.hp2 HG01168.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.539-8506_539-8493d others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | ||||||
| chr16:87860341
|
TACACACA others(9): Show |
T | 5 | a0001c0001t0002g0196a0001c0001t0008g0144a0001c0002t0039g0047others(2): Show | 5 | HG01167.hp1 HG02055.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-8508_539-8493d others(18): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | ||||||
| chr16:87860341
|
TACACACA others(11): Show |
T | 3 | a0001c0002t0006g0002a0001c0002t0006g0045a0001c0002t0010g0046 | 4 | HG02486.hp1 HG02717.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.539-8510_539-8493d others(20): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | ||||||
| chr16:87860341
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0172 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.539-8514_539-8493d others(24): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | ||||||
| chr16:87860343
|
C | T | 53 | a0001c0001t0001g0157a0001c0001t0001g0266a0001c0001t0001g0290others(50): Show | 53 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.539-8494G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860343 | ||||||
| chr16:87860345
|
C | T | 37 | a0001c0001t0001g0157a0001c0001t0001g0266a0001c0001t0001g0290others(34): Show | 37 | HG00438.hp1 HG00639.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.539-8496G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860345 | ||||||
| chr16:87860347
|
C | T | 11 | a0001c0001t0007g0361a0001c0001t0014g0262a0001c0001t0020g0227others(8): Show | 11 | HG00639.hp2 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.539-8498G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860347 | ||||||
| chr16:87860349
|
C | T | 5 | a0001c0001t0005g0166a0001c0001t0034g0006a0001c0001t0062g0353others(2): Show | 5 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-8500G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860349 | ||||||
| chr16:87860351
|
C | T | 10 | a0001c0001t0002g0182a0001c0001t0005g0166a0001c0001t0008g0298others(7): Show | 10 | HG00099.hp2 HG00642.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.539-8502G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860351 | ||||||
| chr16:87860353
|
C | T | 9 | a0001c0001t0007g0327a0001c0001t0007g0328a0001c0001t0008g0298others(6): Show | 9 | HG02630.hp2 HG02723.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.539-8504G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860353 | ||||||
| chr16:87860355
|
C | T | 15 | a0001c0001t0006g0066a0001c0001t0007g0327a0001c0001t0007g0328others(12): Show | 17 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.539-8506G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860355 | ||||||
| chr16:87860357
|
C | T | 14 | a0001c0001t0006g0066a0001c0001t0008g0145a0001c0002t0001g0001others(11): Show | 16 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-8508G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860357 | ||||||
| chr16:87860359
|
C | T | 1 | a0001c0002t0039g0047 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.539-8510G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860359 | ||||||
| chr16:87860361
|
C | T | 3 | a0001c0002t0006g0002a0001c0002t0006g0045a0001c0002t0010g0046 | 4 | HG02486.hp1 HG02717.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.539-8512G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860361 | ||||||
| chr16:87860373
|
CACACACA others(21): Show |
C | 1 | a0001c0001t0005g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.538+8484_538+8511d others(30): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860373 | ||||||
| chr16:87860377
|
CACACACA others(17): Show |
C | 2 | a0001c0001t0012g0059a0001c0001t0012g0060 | 2 | HG01109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.538+8484_538+8507d others(26): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860377 | ||||||
| chr16:87860385
|
CACACACA others(9): Show |
C | 1 | a0001c0001t0003g0332 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.538+8484_538+8499d others(18): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860385 | ||||||
| chr16:87860387
|
CACACACA others(7): Show |
C | 4 | a0001c0001t0002g0097a0001c0001t0003g0336a0001c0001t0003g0350others(1): Show | 4 | HG02683.hp2 HG03492.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+8484_538+8497d others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860387 | ||||||
| chr16:87860389
|
CACACACA others(5): Show |
C | 14 | a0001c0001t0001g0157a0001c0001t0001g0266a0001c0001t0001g0290others(11): Show | 14 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.538+8484_538+8495d others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860389 | ||||||
| chr16:87860391
|
CACACACA others(3): Show |
C | 19 | a0001c0001t0001g0143a0001c0001t0002g0142a0001c0001t0003g0358others(16): Show | 19 | HG00280.hp2 HG00609.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.538+8484_538+8493d others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860391 | ||||||
| chr16:87860393
|
CACACACA others(1): Show |
C | 3 | a0001c0001t0003g0364a0001c0002t0026g0014a0001c0013t0012g0165 | 3 | HG01256.hp1 HG02572.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.538+8484_538+8491d others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860393 | ||||||
| chr16:87860393
|
CACACACA others(3): Show |
C | 4 | a0001c0001t0003g0354a0001c0001t0024g0355a0001c0001t0024g0356others(1): Show | 4 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+8482_538+8491d others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860393 | ||||||
| chr16:87860395
|
C | T | 1 | a0001c0001t0005g0166 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.538+8490G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860395 | ||||||
| chr16:87860395
|
CACACAT | C | 3 | a0001c0002t0005g0009a0001c0002t0010g0011a0001c0002t0012g0050 | 3 | HG00639.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.538+8484_538+8489d others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860395 | ||||||
| chr16:87860397
|
C | T | 12 | a0001c0001t0002g0089a0001c0001t0005g0166a0001c0001t0010g0267others(9): Show | 12 | HG00642.hp1 HG02630.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.538+8488G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860397 | ||||||
| chr16:87860399
|
C | CAT | 4 | a0001c0001t0002g0067a0001c0001t0002g0171a0001c0001t0002g0181others(1): Show | 4 | HG01884.hp1 HG02129.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+8484_538+8485d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860399 | ||||||
| chr16:87860399
|
C | T | 49 | a0001c0001t0002g0089a0001c0001t0002g0190a0001c0001t0004g0178others(46): Show | 51 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.538+8486G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860399 | ||||||
| chr16:87860401
|
T | C | 1 | a0001c0001t0026g0126 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.538+8484A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860401 | ||||||
| chr16:87860409
|
T | A | 1 | a0001c0001t0024g0356 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.538+8476A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860409 | ||||||
| chr16:87860437
|
C | T | 43 | a0001c0001t0001g0157a0001c0001t0001g0266a0001c0001t0001g0290others(40): Show | 43 | HG00438.hp1 HG00639.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.538+8448G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860437 | ||||||
| chr16:87860485
|
G | A | 2 | a0001c0001t0007g0331a0001c0001t0007g0349 | 2 | NA18983.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.538+8400C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860485 | ||||||
| chr16:87860560
|
TCCAGCTG others(4): Show |
T | 8 | a0001c0002t0005g0049a0001c0002t0006g0002a0001c0002t0006g0045others(5): Show | 9 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+8314_538+8324d others(13): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860560 | ||||||
| chr16:87860767
|
G | A | 5 | a0001c0001t0067g0324a0001c0002t0005g0009a0001c0002t0010g0011others(2): Show | 5 | HG00639.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+8118C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860767 | ||||||
| chr16:87860773
|
C | T | 1 | a0001c0001t0014g0052 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.538+8112G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860773 | ||||||
| chr16:87860903
|
G | C | 1 | a0001c0001t0021g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.538+7982C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860903 | ||||||
| chr16:87860930
|
C | T | 2 | a0001c0001t0073g0385a0001c0002t0045g0033 | 2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+7955G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860930 | ||||||
| chr16:87860950
|
C | T | 12 | a0001c0001t0001g0180a0001c0001t0001g0269a0001c0001t0001g0270others(9): Show | 12 | HG00673.hp1 HG00733.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.538+7935G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860950 | ||||||
| chr16:87860955
|
G | A | 5 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250others(2): Show | 5 | HG00738.hp1 HG01978.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.538+7930C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860955 | ||||||
| chr16:87860986
|
C | T | 8 | a0001c0002t0005g0049a0001c0002t0006g0002a0001c0002t0006g0045others(5): Show | 9 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+7899G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860986 | ||||||
| chr16:87861055
|
G | C | 2 | a0001c0001t0003g0378a0001c0001t0013g0155 | 2 | HG01168.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.538+7830C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861055 | ||||||
| chr16:87861085
|
G | A | 5 | a0001c0001t0067g0324a0001c0002t0005g0009a0001c0002t0010g0011others(2): Show | 5 | HG00639.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+7800C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861085 | ||||||
| chr16:87861116
|
G | C | 32 | a0001c0001t0005g0166a0001c0001t0006g0066a0001c0001t0006g0164others(29): Show | 34 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.538+7769C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861116 | ||||||
| chr16:87861151
|
G | A | 1 | a0001c0001t0003g0372 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.538+7734C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861151 | ||||||
| chr16:87861215
|
G | A | 1 | a0001c0001t0005g0098 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.538+7670C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861215 | ||||||
| chr16:87861255
|
G | A | 1 | a0001c0002t0001g0001 | 3 | HG01069.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.538+7630C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861255 | ||||||
| chr16:87861448
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.538+7437C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861448 | ||||||
| chr16:87861493
|
G | A | 1 | a0001c0002t0005g0049 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.538+7392C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861493 | ||||||
| chr16:87861500
|
C | A | 1 | a0001c0001t0067g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538+7385G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861500 | ||||||
| chr16:87861565
|
GGCCAAGA others(14): Show |
G | 1 | a0001c0001t0002g0196 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.538+7299_538+7319d others(23): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861565 | ||||||
| chr16:87861680
|
C | G | 5 | a0001c0001t0005g0058a0001c0001t0012g0059a0001c0001t0012g0060others(2): Show | 5 | HG01109.hp1 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+7205G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861680 | ||||||
| chr16:87861838
|
C | G | 3 | a0001c0001t0005g0186a0001c0001t0005g0187a0001c0001t0005g0188 | 3 | HG01175.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.538+7047G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861838 | ||||||
| chr16:87861888
|
C | T | 2 | a0001c0005t0031g0381a0001c0005t0031g0383 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.538+6997G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861888 | ||||||
| chr16:87861930
|
A | G | 1 | a0001c0002t0066g0320 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.538+6955T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861930 | ||||||
| chr16:87862216
|
C | T | 4 | a0001c0002t0026g0014a0001c0002t0027g0016a0001c0002t0027g0017others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+6669G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862216 | ||||||
| chr16:87862228
|
T | G | 5 | a0001c0002t0006g0023a0001c0002t0006g0024a0001c0002t0006g0025others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+6657A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862228 | ||||||
| chr16:87862253
|
T | C | 5 | a0001c0001t0067g0324a0001c0002t0005g0009a0001c0002t0010g0011others(2): Show | 5 | HG00639.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+6632A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862253 | ||||||
| chr16:87862415
|
G | A | 3 | a0003c0006t0008g0309a0003c0006t0008g0310a0003c0006t0014g0308 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.538+6470C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862415 | ||||||
| chr16:87862443
|
A | G | 3 | a0001c0001t0001g0107a0001c0001t0004g0114a0008c0007t0001g0007 | 3 | HG01978.hp1 HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.538+6442T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862443 | ||||||
| chr16:87862454
|
T | C | 1 | a0001c0001t0002g0279 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.538+6431A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862454 | ||||||
| chr16:87862639
|
G | C | 7 | a0001c0001t0016g0285a0001c0001t0016g0286a0001c0001t0016g0287others(4): Show | 7 | HG01167.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.538+6246C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862639 | ||||||
| chr16:87862851
|
T | C | 3 | a0001c0001t0005g0058a0001c0001t0012g0059a0001c0001t0012g0060 | 3 | HG01109.hp1 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.538+6034A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862851 | ||||||
| chr16:87862992
|
C | T | 1 | a0001c0001t0022g0170 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.538+5893G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862992 | ||||||
| chr16:87863010
|
G | A | 1 | a0003c0006t0008g0310 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.538+5875C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863010 | ||||||
| chr16:87863130
|
C | T | 1 | a0001c0001t0033g0360 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.538+5755G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863130 | ||||||
| chr16:87863131
|
G | A | 25 | a0001c0001t0004g0283a0001c0001t0010g0267a0001c0001t0010g0288others(22): Show | 26 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.538+5754C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863131 | ||||||
| chr16:87863272
|
T | C | 1 | a0001c0002t0012g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.538+5613A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863272 | ||||||
| chr16:87863354
|
G | A | 2 | a0001c0001t0002g0302a0001c0001t0009g0209 | 2 | HG02738.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.538+5531C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863354 | ||||||
| chr16:87863443
|
C | T | 1 | a0001c0001t0003g0332 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.538+5442G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863443 | ||||||
| chr16:87863452
|
A | T | 6 | a0001c0001t0014g0052a0001c0001t0014g0259a0001c0001t0014g0260others(3): Show | 6 | HG02897.hp2 HG02970.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.538+5433T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863452 | ||||||
| chr16:87863610
|
G | A | 1 | a0001c0001t0006g0177 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.538+5275C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863610 | ||||||
| chr16:87863731
|
G | A | 8 | a0001c0002t0005g0049a0001c0002t0006g0002a0001c0002t0006g0045others(5): Show | 9 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+5154C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863731 | ||||||
| chr16:87863788
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.538+5097G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863788 | ||||||
| chr16:87863792
|
C | T | 1 | a0001c0002t0020g0028 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.538+5093G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863792 | ||||||
| chr16:87863872
|
G | A | 3 | a0001c0005t0031g0381a0001c0005t0031g0383a0001c0005t0063g0382 | 3 | HG01081.hp2 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.538+5013C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863872 | ||||||
| chr16:87863892
|
T | C | 1 | a0001c0001t0049g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.538+4993A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863892 | ||||||
| chr16:87863913
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.538+4972T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863913 | ||||||
| chr16:87863967
|
TTATGTGT others(25): Show |
T | 1 | a0001c0003t0001g0070 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.538+4886_538+4917d others(34): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863967 | ||||||
| chr16:87863982
|
T | TAAAAAA | 8 | a0001c0001t0010g0267a0001c0001t0010g0288a0001c0002t0008g0037others(5): Show | 8 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.538+4902_538+4903i others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863982 | ||||||
| chr16:87863984
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0003g0346 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.538+4900_538+4901i others(17): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863984 | ||||||
| chr16:87863986
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.538+4898_538+4899i others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AAAAAAAA others(11): Show |
6 | a0001c0001t0004g0283a0001c0001t0018g0313a0001c0001t0018g0314others(3): Show | 6 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.538+4898_538+4899i others(20): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AAAATATA others(11): Show |
1 | a0001c0001t0005g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.538+4898_538+4899i others(20): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AAAATATA others(13): Show |
1 | a0001c0013t0012g0165 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.538+4898_538+4899i others(22): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AAT | 8 | a0001c0002t0005g0049a0001c0002t0006g0002a0001c0002t0006g0045others(5): Show | 9 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+4897_538+4898d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATACATA others(5): Show |
3 | a0001c0001t0001g0266a0001c0001t0004g0264a0001c0001t0004g0265 | 3 | HG00438.hp1 HG02165.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.538+4898_538+4899i others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATAT | 4 | a0001c0002t0012g0050a0001c0002t0026g0014a0001c0002t0027g0016others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+4895_538+4898d others(6): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATAT | 9 | a0001c0001t0006g0066a0001c0001t0006g0164a0001c0001t0008g0144others(6): Show | 9 | HG01167.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+4893_538+4898d others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(1): Show |
8 | a0001c0001t0005g0058a0001c0001t0011g0377a0001c0001t0012g0059others(5): Show | 8 | HG01109.hp1 HG01516.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.538+4891_538+4898d others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(3): Show |
15 | a0001c0001t0014g0052a0001c0001t0014g0259a0001c0001t0014g0260others(12): Show | 17 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.538+4889_538+4898d others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(5): Show |
91 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0119others(88): Show | 92 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.538+4887_538+4898d others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(7): Show |
43 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0065others(40): Show | 44 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.538+4885_538+4898d others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(9): Show |
43 | a0001c0001t0001g0069a0001c0001t0001g0103a0001c0001t0001g0194others(40): Show | 43 | HG00673.hp1 HG00733.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.538+4883_538+4898d others(18): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(11): Show |
48 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0151others(45): Show | 48 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.538+4881_538+4898d others(20): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(13): Show |
31 | a0001c0001t0001g0068a0001c0001t0001g0082a0001c0001t0001g0172others(28): Show | 31 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.538+4879_538+4898d others(22): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(15): Show |
17 | a0001c0001t0001g0149a0001c0001t0002g0171a0001c0001t0002g0274others(14): Show | 17 | HG00140.hp1 HG01081.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.538+4877_538+4898d others(24): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(17): Show |
11 | a0001c0001t0002g0067a0001c0001t0002g0077a0001c0001t0002g0147others(8): Show | 11 | HG00738.hp1 HG01192.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.538+4898_538+4899i others(26): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(19): Show |
10 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0076others(7): Show | 10 | HG00741.hp2 HG01099.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.538+4898_538+4899i others(28): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(21): Show |
4 | a0001c0001t0002g0284a0001c0001t0003g0370a0001c0001t0030g0311others(1): Show | 4 | HG00280.hp1 HG01074.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+4898_538+4899i others(30): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(23): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0248 | 3 | HG01993.hp2 HG02683.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.538+4898_538+4899i others(32): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(25): Show |
4 | a0001c0001t0007g0344a0001c0001t0007g0345a0001c0001t0013g0167others(1): Show | 4 | HG00639.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+4898_538+4899i others(34): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(27): Show |
1 | a0006c0012t0002g0292 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.538+4898_538+4899i others(36): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(33): Show |
1 | a0001c0001t0007g0329 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.538+4898_538+4899i others(42): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(37): Show |
3 | a0001c0001t0001g0071a0001c0001t0007g0342a0001c0001t0007g0343 | 3 | HG02071.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.538+4898_538+4899i others(46): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | AATATATA others(39): Show |
1 | a0001c0001t0002g0133 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.538+4898_538+4899i others(48): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0138 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.538+4898_538+4899i others(15): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0330 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.538+4898_538+4899i others(23): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863986
|
A | T | 1 | a0001c0001t0003g0346 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.538+4899T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | ||||||
| chr16:87863998
|
T | C | 6 | a0001c0001t0004g0283a0001c0001t0018g0313a0001c0001t0018g0314others(3): Show | 6 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.538+4887A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863998 | ||||||
| chr16:87864020
|
G | A | 2 | a0001c0002t0023g0317a0001c0002t0023g0318 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.538+4865C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864020 | ||||||
| chr16:87864030
|
G | A | 4 | a0001c0001t0025g0351a0001c0002t0005g0009a0001c0002t0010g0011others(1): Show | 4 | HG00639.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+4855C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864030 | ||||||
| chr16:87864108
|
G | A | 1 | a0001c0001t0006g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.538+4777C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864108 | ||||||
| chr16:87864269
|
A | G | 65 | a0001c0001t0004g0283a0001c0001t0005g0058a0001c0001t0005g0166others(62): Show | 68 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.538+4616T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864269 | ||||||
| chr16:87864279
|
C | A | 2 | a0001c0001t0029g0161a0001c0001t0029g0162 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.538+4606G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864279 | ||||||
| chr16:87864435
|
G | A | 9 | a0001c0001t0010g0267a0001c0001t0010g0288a0001c0002t0008g0037others(6): Show | 9 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+4450C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864435 | ||||||
| chr16:87864571
|
A | C | 7 | a0001c0002t0005g0009a0001c0002t0010g0011a0001c0002t0012g0050others(4): Show | 7 | HG00639.hp2 HG01081.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+4314T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864571 | ||||||
| chr16:87864598
|
T | C | 19 | a0001c0001t0001g0127a0001c0001t0001g0232a0001c0001t0001g0233others(16): Show | 19 | HG00408.hp1 HG00544.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.538+4287A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864598 | ||||||
| chr16:87864754
|
A | G | 1 | a0001c0001t0003g0341 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.538+4131T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864754 | ||||||
| chr16:87864886
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.538+3999T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864886 | ||||||
| chr16:87864935
|
G | A | 4 | a0001c0001t0006g0128a0001c0001t0006g0129a0001c0001t0006g0130others(1): Show | 4 | HG01243.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+3950C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864935 | ||||||
| chr16:87864990
|
C | G | 1 | a0001c0002t0020g0028 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.538+3895G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864990 | ||||||
| chr16:87865144
|
T | C | 1 | a0001c0001t0062g0353 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.538+3741A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865144 | ||||||
| chr16:87865327
|
C | T | 3 | a0001c0001t0018g0313a0001c0001t0018g0314a0001c0001t0018g0315 | 3 | HG01070.hp2 HG01071.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.538+3558G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865327 | ||||||
| chr16:87865436
|
T | C | 63 | a0001c0001t0004g0283a0001c0001t0005g0058a0001c0001t0006g0066others(60): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.538+3449A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865436 | ||||||
| chr16:87865480
|
G | A | 2 | a0001c0005t0031g0381a0001c0005t0031g0383 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.538+3405C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865480 | ||||||
| chr16:87865621
|
C | T | 1 | a0001c0005t0031g0381 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.538+3264G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865621 | ||||||
| chr16:87865663
|
T | C | 35 | a0001c0001t0006g0066a0001c0001t0006g0164a0001c0001t0008g0144others(32): Show | 38 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.538+3222A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865663 | ||||||
| chr16:87865708
|
G | C | 8 | a0001c0001t0020g0227a0001c0002t0006g0023a0001c0002t0006g0024others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.538+3177C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865708 | ||||||
| chr16:87865732
|
T | A | 8 | a0001c0001t0020g0227a0001c0002t0006g0023a0001c0002t0006g0024others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.538+3153A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865732 | ||||||
| chr16:87865787
|
T | G | 3 | a0001c0001t0034g0006a0001c0002t0001g0035a0004c0014t0035g0005 | 3 | HG02723.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.538+3098A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865787 | ||||||
| chr16:87865832
|
C | G | 11 | a0001c0001t0020g0227a0001c0001t0034g0006a0001c0002t0001g0035others(8): Show | 11 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.538+3053G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865832 | ||||||
| chr16:87865846
|
G | A | 3 | a0001c0001t0034g0006a0001c0002t0001g0035a0004c0014t0035g0005 | 3 | HG02723.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.538+3039C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865846 | ||||||
| chr16:87865849
|
C | T | 1 | a0001c0013t0012g0165 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.538+3036G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865849 | ||||||
| chr16:87865878
|
T | C | 1 | a0001c0001t0004g0226 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.538+3007A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865878 | ||||||
| chr16:87865892
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.538+2993G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865892 | ||||||
| chr16:87865901
|
G | A | 2 | a0001c0001t0006g0164a0001c0001t0040g0163 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.538+2984C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865901 | ||||||
| chr16:87865963
|
G | A | 1 | a0001c0001t0067g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538+2922C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865963 | ||||||
| chr16:87865979
|
G | C | 37 | a0001c0001t0001g0266a0001c0001t0001g0290a0001c0001t0003g0330others(34): Show | 37 | HG00438.hp1 HG00438.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.538+2906C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865979 | ||||||
| chr16:87866015
|
A | G | 10 | a0001c0001t0020g0227a0001c0002t0006g0023a0001c0002t0006g0024others(7): Show | 10 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.538+2870T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866015 | ||||||
| chr16:87866091
|
T | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0149a0001c0001t0001g0151others(84): Show | 91 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.538+2794A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866091 | ||||||
| chr16:87866097
|
G | C | 3 | a0001c0001t0002g0133a0001c0001t0002g0134a0001c0001t0002g0135 | 3 | NA18977.hp1 NA19009.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.538+2788C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866097 | ||||||
| chr16:87866110
|
T | G | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0138others(145): Show | 153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.538+2775A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866110 | ||||||
| chr16:87866266
|
G | A | 11 | a0001c0002t0001g0013a0001c0002t0001g0018a0001c0002t0001g0019others(8): Show | 11 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.538+2619C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866266 | ||||||
| chr16:87866267
|
G | C | 7 | a0001c0002t0006g0023a0001c0002t0006g0024a0001c0002t0006g0025others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+2618C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866267 | ||||||
| chr16:87866272
|
C | T | 7 | a0001c0002t0006g0002a0001c0002t0006g0045a0001c0002t0010g0046others(4): Show | 8 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.538+2613G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866272 | ||||||
| chr16:87866300
|
G | A | 1 | a0001c0001t0002g0284 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.538+2585C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866300 | ||||||
| chr16:87866305
|
A | G | 2 | a0001c0001t0011g0325a0001c0001t0025g0326 | 2 | HG01070.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.538+2580T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866305 | ||||||
| chr16:87866334
|
G | C | 7 | a0001c0001t0010g0288a0001c0001t0016g0285a0001c0001t0016g0286others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+2551C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866334 | ||||||
| chr16:87866383
|
T | C | 156 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0065others(153): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.538+2502A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866383 | ||||||
| chr16:87866436
|
G | A | 21 | a0001c0001t0001g0266a0001c0001t0004g0264a0001c0001t0004g0265others(18): Show | 21 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.538+2449C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866436 | ||||||
| chr16:87866478
|
T | C | 10 | a0001c0001t0010g0267a0001c0002t0001g0035a0001c0002t0008g0037others(7): Show | 10 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.538+2407A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866478 | ||||||
| chr16:87866489
|
G | A | 1 | a0001c0001t0065g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.538+2396C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866489 | ||||||
| chr16:87866496
|
C | T | 1 | a0001c0001t0067g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538+2389G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866496 | ||||||
| chr16:87866503
|
T | C | 2 | a0001c0001t0034g0006a0004c0014t0035g0005 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.538+2382A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866503 | ||||||
| chr16:87866506
|
C | T | 9 | a0001c0002t0001g0035a0001c0002t0008g0037a0001c0002t0008g0038others(6): Show | 9 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+2379G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866506 | ||||||
| chr16:87866596
|
G | C | 7 | a0001c0001t0010g0288a0001c0001t0016g0285a0001c0001t0016g0286others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+2289C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866596 | ||||||
| chr16:87866647
|
A | G | 1 | a0001c0001t0073g0385 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.538+2238T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866647 | ||||||
| chr16:87866686
|
C | T | 6 | a0001c0001t0010g0288a0001c0001t0016g0285a0001c0001t0016g0286others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.538+2199G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866686 | ||||||
| chr16:87866692
|
C | T | 1 | a0001c0002t0045g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.538+2193G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866692 | ||||||
| chr16:87866763
|
G | C | 22 | a0001c0002t0001g0013a0001c0002t0001g0018a0001c0002t0001g0019others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.538+2122C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866763 | ||||||
| chr16:87866842
|
C | A | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.538+2043G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866842 | ||||||
| chr16:87866919
|
G | C | 16 | a0001c0002t0001g0013a0001c0002t0001g0018a0001c0002t0001g0019others(13): Show | 16 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.538+1966C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866919 | ||||||
| chr16:87866934
|
G | A | 10 | a0001c0002t0001g0001a0001c0002t0002g0048a0001c0002t0005g0049others(7): Show | 13 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.538+1951C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866934 | ||||||
| chr16:87866957
|
A | G | 9 | a0001c0002t0001g0035a0001c0002t0008g0037a0001c0002t0008g0038others(6): Show | 9 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+1928T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866957 | ||||||
| chr16:87866994
|
G | C | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0006g0271others(1): Show | 4 | HG00673.hp1 HG02015.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+1891C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866994 | ||||||
| chr16:87867020
|
A | G | 371 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(368): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.538+1865T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867020 | ||||||
| chr16:87867033
|
C | T | 1 | a0001c0001t0067g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538+1852G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867033 | ||||||
| chr16:87867071
|
C | T | 10 | a0001c0002t0001g0001a0001c0002t0002g0048a0001c0002t0005g0049others(7): Show | 13 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.538+1814G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867071 | ||||||
| chr16:87867172
|
G | A | 1 | a0001c0001t0016g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.538+1713C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867172 | ||||||
| chr16:87867200
|
G | A | 23 | a0001c0002t0001g0013a0001c0002t0001g0018a0001c0002t0001g0019others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.538+1685C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867200 | ||||||
| chr16:87867218
|
C | A | 1 | a0001c0001t0036g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.538+1667G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867218 | ||||||
| chr16:87867218
|
C | T | 4 | a0001c0002t0008g0042a0002c0004t0019g0044a0002c0004t0043g0041others(1): Show | 4 | HG02630.hp2 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+1667G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867218 | ||||||
| chr16:87867254
|
G | A | 6 | a0001c0001t0010g0288a0001c0001t0016g0285a0001c0001t0016g0286others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.538+1631C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867254 | ||||||
| chr16:87867268
|
C | T | 23 | a0001c0002t0001g0013a0001c0002t0001g0018a0001c0002t0001g0019others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.538+1617G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867268 | ||||||
| chr16:87867303
|
C | G | 1 | a0001c0001t0014g0052 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.538+1582G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867303 | ||||||
| chr16:87867306
|
G | A | 7 | a0001c0001t0018g0313a0001c0001t0018g0314a0001c0001t0018g0315others(4): Show | 7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+1579C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867306 | ||||||
| chr16:87867309
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.538+1576C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867309 | ||||||
| chr16:87867385
|
C | A | 64 | a0001c0001t0001g0290a0001c0001t0003g0330a0001c0001t0003g0332others(61): Show | 64 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.538+1500G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867385 | ||||||
| chr16:87867429
|
C | A | 1 | a0001c0001t0004g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.538+1456G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867429 | ||||||
| chr16:87867472
|
A | G | 87 | a0001c0001t0001g0290a0001c0001t0003g0330a0001c0001t0003g0332others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.538+1413T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867472 | ||||||
| chr16:87867549
|
C | G | 3 | a0001c0005t0031g0381a0001c0005t0031g0383a0001c0005t0063g0382 | 3 | HG01081.hp2 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.538+1336G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867549 | ||||||
| chr16:87867564
|
C | T | 1 | a0001c0002t0055g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.538+1321G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867564 | ||||||
| chr16:87867595
|
C | T | 1 | a0001c0001t0006g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.538+1290G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867595 | ||||||
| chr16:87867681
|
T | C | 7 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(4): Show | 7 | HG00438.hp2 HG02132.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+1204A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867681 | ||||||
| chr16:87867703
|
G | C | 86 | a0001c0001t0001g0290a0001c0001t0003g0330a0001c0001t0003g0332others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.538+1182C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867703 | ||||||
| chr16:87867840
|
G | A | 22 | a0001c0002t0001g0013a0001c0002t0001g0018a0001c0002t0001g0019others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.538+1045C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867840 | ||||||
| chr16:87867853
|
C | A | 2 | a0001c0001t0001g0305a0001c0001t0004g0291 | 2 | HG02015.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.538+1032G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867853 | ||||||
| chr16:87867886
|
C | T | 1 | a0001c0002t0001g0001 | 3 | HG01069.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.538+999G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867886 | ||||||
| chr16:87868057
|
G | A | 125 | a0001c0001t0003g0330a0001c0001t0003g0332a0001c0001t0003g0336others(122): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.538+828C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868057 | ||||||
| chr16:87868104
|
G | A | 52 | a0001c0002t0001g0001a0001c0002t0001g0013a0001c0002t0001g0018others(49): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.538+781C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868104 | ||||||
| chr16:87868115
|
C | CA | 76 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(73): Show | 76 | HG00323.hp2 HG00673.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.538+769dupT | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868115 | ||||||
| chr16:87868115
|
C | CAA | 6 | a0001c0001t0005g0058a0001c0001t0011g0375a0001c0001t0011g0376others(3): Show | 6 | HG00438.hp2 HG01109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.538+768_538+769dup others(2): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868115 | ||||||
| chr16:87868129
|
A | G | 1 | a0001c0002t0010g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.538+756T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868129 | ||||||
| chr16:87868130
|
A | G | 48 | a0001c0001t0001g0065a0001c0001t0015g0062a0001c0001t0015g0063others(45): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.538+755T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868130 | ||||||
| chr16:87868132
|
A | G | 7 | a0001c0002t0006g0023a0001c0002t0006g0024a0001c0002t0006g0025others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+753T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868132 | ||||||
| chr16:87868132
|
AAG | A | 44 | a0001c0002t0001g0001a0001c0002t0001g0013a0001c0002t0001g0018others(41): Show | 47 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.538+751_538+752del others(2): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868132 | ||||||
| chr16:87868134
|
G | A | 7 | a0001c0002t0006g0023a0001c0002t0006g0024a0001c0002t0006g0025others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+751C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868134 | ||||||
| chr16:87868157
|
A | G | 1 | a0001c0001t0036g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.538+728T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868157 | ||||||
| chr16:87868258
|
G | A | 1 | a0001c0002t0055g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.538+627C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868258 | ||||||
| chr16:87868278
|
A | C | 52 | a0001c0002t0001g0001a0001c0002t0001g0013a0001c0002t0001g0018others(49): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.538+607T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868278 | ||||||
| chr16:87868320
|
G | C | 10 | a0001c0002t0001g0035a0001c0002t0008g0037a0001c0002t0008g0038others(7): Show | 10 | HG02630.hp1 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.538+565C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868320 | ||||||
| chr16:87868350
|
T | C | 52 | a0001c0002t0001g0001a0001c0002t0001g0013a0001c0002t0001g0018others(49): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.538+535A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868350 | ||||||
| chr16:87868361
|
C | T | 1 | a0001c0001t0050g0057 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.538+524G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868361 | ||||||
| chr16:87868378
|
G | T | 37 | a0001c0002t0001g0013a0001c0002t0001g0018a0001c0002t0001g0019others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.538+507C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868378 | ||||||
| chr16:87868400
|
G | A | 1 | a0001c0001t0011g0377 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.538+485C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868400 | ||||||
| chr16:87868402
|
G | C | 52 | a0001c0002t0001g0001a0001c0002t0001g0013a0001c0002t0001g0018others(49): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.538+483C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868402 | ||||||
| chr16:87868503
|
G | A | 7 | a0001c0001t0018g0313a0001c0001t0018g0314a0001c0001t0018g0315others(4): Show | 7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+382C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868503 | ||||||
| chr16:87868510
|
T | C | 1 | a0001c0001t0006g0306 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.538+375A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868510 | ||||||
| chr16:87868542
|
T | C | 1 | a0001c0001t0003g0378 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.538+343A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868542 | ||||||
| chr16:87868593
|
G | C | 120 | a0001c0001t0003g0330a0001c0001t0003g0332a0001c0001t0003g0336others(117): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.538+292C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868593 | ||||||
| chr16:87868606
|
A | G | 119 | a0001c0001t0003g0330a0001c0001t0003g0332a0001c0001t0003g0336others(116): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.538+279T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868606 | ||||||
| chr16:87868610
|
C | T | 1 | a0004c0015t0042g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.538+275G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868610 | ||||||
| chr16:87868649
|
G | T | 1 | a0001c0001t0017g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.538+236C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868649 | ||||||
| chr16:87868654
|
G | A | 7 | a0001c0001t0018g0313a0001c0001t0018g0314a0001c0001t0018g0315others(4): Show | 7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+231C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868654 | ||||||
| chr16:87868721
|
G | T | 1 | a0001c0001t0004g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.538+164C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868721 | ||||||
| chr16:87868737
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.538+148G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868737 | ||||||
| chr16:87868767
|
C | T | 1 | a0001c0001t0014g0052 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.538+118G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868767 |