| geneid | 151258 |
|---|---|
| ensemblid | ENSG00000169507.10 |
| hgncid | 26836 |
| symbol | SLC38A11 |
| name | solute carrier family 38 member 11 |
| refseq_nuc | NM_001351537.2 |
| refseq_prot | NP_001338466.1 |
| ensembl_nuc | ENST00000685975.1 |
| ensembl_prot | ENSP00000508649.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 164894354 |
| end | 164955525 |
| strand | - |
| ver | v1.2 |
| region | chr2:164894354-164955525 |
| region5000 | chr2:164889354-164960525 |
| regionname0 | SLC38A11_chr2_164894354_164955525 |
| regionname5000 | SLC38A11_chr2_164889354_164960525 |
| 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 | 462 | 352 | 77 | 66 | 163 | 14 | 30 | 124 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0002 | 0/0 | 462 | 18 | 0 | 0 | 17 | 0 | 1 | 13 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0003 | 0/0 | 462 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0004 | 0/0 | 462 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0005 | 0/0 | 462 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0006 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1389 | 338 | 63 | 66 | 163 | 14 | 30 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| c0002 | 0/0 | 1389 | 18 | 0 | 0 | 17 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| c0003 | 0/0 | 1389 | 14 | 14 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| c0004 | 0/0 | 1389 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| c0005 | 0/0 | 1389 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| c0006 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| c0007 | 0/0 | 1389 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| 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 | 0/1 | 4363 | 105 | 3 | 15 | 70 | 3 | 13 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0002 | 0/0 | 4362 | 92 | 28 | 31 | 19 | 8 | 6 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0003 | 0/0 | 4361 | 55 | 1 | 8 | 34 | 3 | 9 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0004 | 0/0 | 4361 | 23 | 0 | 0 | 23 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0005 | 1/0 | 4362 | 17 | 15 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0006 | 0/0 | 4362 | 14 | 0 | 0 | 14 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0007 | 0/0 | 4362 | 12 | 10 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0008 | 0/0 | 4363 | 11 | 0 | 0 | 11 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0009 | 0/0 | 4357 | 6 | 0 | 0 | 6 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0010 | 0/0 | 4363 | 5 | 5 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0011 | 0/0 | 4362 | 4 | 2 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0012 | 0/0 | 4362 | 4 | 1 | 2 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0013 | 0/0 | 4361 | 3 | 3 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0014 | 0/0 | 4362 | 2 | 0 | 1 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0015 | 0/0 | 4362 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0016 | 0/0 | 4362 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0017 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0018 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0019 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0020 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0021 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0022 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0023 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0024 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0025 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0026 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0027 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0028 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0029 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0030 | 0/0 | 4361 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0031 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0032 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0033 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0034 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| t0035 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| 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 | 6 | 0 | 0 | 5 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0002 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0003 | 1/0 | 5 | 4 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0009 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1389 | 338 | 63 | 66 | 163 | 14 | 30 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0003 | 0/0 | 1389 | 14 | 14 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0002c0002 | 0/0 | 1389 | 18 | 0 | 0 | 17 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0003c0004 | 0/0 | 1389 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0004c0005 | 0/0 | 1389 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0005c0007 | 0/0 | 1389 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0006c0006 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5751 | 102 | 3 | 15 | 67 | 3 | 13 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0002 | 0/0 | 5750 | 77 | 14 | 31 | 19 | 8 | 5 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0003 | 0/0 | 5749 | 55 | 1 | 8 | 34 | 3 | 9 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0004 | 0/0 | 5749 | 22 | 0 | 0 | 22 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0005 | 1/0 | 5750 | 17 | 15 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0006 | 0/0 | 5750 | 14 | 0 | 0 | 14 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0007 | 0/0 | 5750 | 12 | 10 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0010 | 0/0 | 5751 | 4 | 4 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0011 | 0/0 | 5750 | 4 | 2 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0012 | 0/0 | 5750 | 4 | 1 | 2 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0013 | 0/0 | 5749 | 3 | 3 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0014 | 0/0 | 5750 | 2 | 0 | 1 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0015 | 0/0 | 5750 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0016 | 0/0 | 5750 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0017 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0018 | 0/0 | 5750 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0019 | 0/0 | 5751 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0020 | 0/0 | 5751 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0021 | 0/0 | 5751 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0022 | 0/0 | 5751 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0023 | 0/0 | 5749 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0024 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0025 | 0/0 | 5750 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0026 | 0/0 | 5751 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0027 | 0/0 | 5750 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0028 | 0/0 | 5749 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0029 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0030 | 0/0 | 5749 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0032 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0033 | 0/0 | 5750 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0034 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0001t0035 | 0/0 | 5750 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0001c0003t0002 | 0/0 | 5750 | 14 | 14 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0002c0002t0008 | 0/0 | 5751 | 11 | 0 | 0 | 11 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0002c0002t0009 | 0/0 | 5745 | 6 | 0 | 0 | 6 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0002c0002t0031 | 0/0 | 5750 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0003c0004t0001 | 0/0 | 5751 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0004c0005t0002 | 0/0 | 5750 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0005c0007t0004 | 0/0 | 5749 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| a0006c0006t0010 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | copy fasta | chr2 | 164889354 | 164960525 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0005g0003 | 1/0 | 5 | 4 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0005g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0005g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0006g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0006g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0006g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0007g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0010g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0010g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0010g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0010g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0011g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0011g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0011g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0011g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0012g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0012g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0012g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0013g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0013g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0013g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0014g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0014g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0015g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0015g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0016g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0016g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0017g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0018g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0019g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0020g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0021g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0022g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0023g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0024g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0025g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0026g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0027g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0028g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0029g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0030g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0032g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0033g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0034g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0035g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0003t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0003t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0003t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0003t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0003t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0003t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0003t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0003t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0003t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0003t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0003t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0008g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0008g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0008g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0008g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0008g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0008g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0008g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0008g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0008g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0008g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0009g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0009g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0009g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0009g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0009g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0002c0002t0031g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0003c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0003c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0003c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0004c0005t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0005c0007t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0006c0006t0010g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0264 | EUR | GBR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | GBR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0213 | EUR | GBR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | GBR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | FIN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00408 | hp2 | a0001 | c0001 | t0030 | g0070 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00423 | hp2 | a0002 | c0002 | t0009 | g0041 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00597 | hp1 | a0005 | c0007 | t0004 | g0228 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00642 | hp1 | a0001 | c0001 | t0014 | g0107 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0191 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01074 | hp1 | a0001 | c0001 | t0021 | g0116 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01106 | hp2 | a0001 | c0001 | t0027 | g0180 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01109 | hp2 | a0001 | c0001 | t0026 | g0218 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01175 | hp2 | a0001 | c0001 | t0011 | g0184 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0275 | AMR | PUR | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0046 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01261 | hp2 | a0001 | c0001 | t0022 | g0166 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01358 | hp1 | a0001 | c0001 | t0011 | g0181 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0190 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0014 | EUR | IBS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | IBS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0274 | EUR | IBS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0273 | EUR | IBS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | IBS | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01952 | hp2 | a0001 | c0001 | t0033 | g0055 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02040 | hp1 | a0002 | c0002 | t0009 | g0311 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0256 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02135 | hp1 | a0001 | c0001 | t0020 | g0111 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0257 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | CDX | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CDX | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0290 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02258 | hp1 | a0001 | c0001 | t0016 | g0258 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02273 | hp1 | a0001 | c0001 | t0012 | g0036 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0252 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0174 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02300 | hp2 | a0001 | c0001 | t0012 | g0036 | AMR | PEL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0192 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02523 | hp1 | a0002 | c0002 | t0009 | g0301 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0173 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0188 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02615 | hp2 | a0001 | c0001 | t0024 | g0175 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02622 | hp1 | a0001 | c0001 | t0017 | g0220 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02622 | hp2 | a0001 | c0001 | t0015 | g0267 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0185 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02630 | hp2 | a0001 | c0001 | t0029 | g0284 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02647 | hp1 | a0001 | c0003 | t0002 | g0024 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0187 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02723 | hp2 | a0001 | c0003 | t0002 | g0023 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0136 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0294 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0163 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0024 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02897 | hp2 | a0001 | c0003 | t0002 | g0183 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02922 | hp1 | a0001 | c0001 | t0016 | g0262 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02970 | hp1 | a0006 | c0006 | t0010 | g0254 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02970 | hp2 | a0001 | c0001 | t0034 | g0261 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0196 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0287 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0165 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0295 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0194 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0286 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0023 | AFR | MSL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0195 | AFR | MSL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | MSL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0164 | AFR | MSL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03486 | hp1 | a0001 | c0003 | t0002 | g0171 | AFR | MSL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0251 | AFR | MSL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03490 | hp1 | a0004 | c0005 | t0002 | g0219 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0189 | AFR | ESN | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03540 | hp1 | a0001 | c0001 | t0032 | g0280 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0243 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03710 | hp1 | a0002 | c0002 | t0031 | g0283 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | BEB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03831 | hp2 | a0001 | c0001 | t0018 | g0222 | SAS | BEB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | BEB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0093 | SAS | STU | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | STU | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | STU | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | CHB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18612 | hp2 | a0002 | c0002 | t0008 | g0297 | EAS | CHB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0293 | AFR | YRI | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0250 | AFR | YRI | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18939 | hp1 | a0001 | c0001 | t0035 | g0231 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18940 | hp1 | a0002 | c0002 | t0008 | g0307 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18940 | hp2 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18942 | hp1 | a0002 | c0002 | t0008 | g0303 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18946 | hp2 | a0002 | c0002 | t0008 | g0302 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18951 | hp1 | a0001 | c0001 | t0006 | g0232 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18962 | hp2 | a0002 | c0002 | t0008 | g0308 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18970 | hp1 | a0002 | c0002 | t0009 | g0300 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18973 | hp1 | a0001 | c0001 | t0006 | g0206 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18975 | hp2 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18977 | hp1 | a0001 | c0001 | t0019 | g0224 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0207 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18983 | hp2 | a0002 | c0002 | t0008 | g0306 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18986 | hp1 | a0003 | c0004 | t0001 | g0090 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18986 | hp2 | a0001 | c0001 | t0006 | g0203 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18987 | hp2 | a0001 | c0001 | t0023 | g0241 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18989 | hp2 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18991 | hp1 | a0002 | c0002 | t0008 | g0299 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18997 | hp1 | a0001 | c0001 | t0025 | g0088 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18998 | hp1 | a0003 | c0004 | t0001 | g0137 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18999 | hp1 | a0002 | c0002 | t0008 | g0305 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19001 | hp1 | a0002 | c0002 | t0009 | g0298 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19006 | hp2 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | LWK | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19030 | hp2 | a0001 | c0001 | t0011 | g0182 | AFR | LWK | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | LWK | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0277 | AFR | LWK | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19065 | hp1 | a0002 | c0002 | t0008 | g0310 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19066 | hp1 | a0003 | c0004 | t0001 | g0138 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19067 | hp1 | a0001 | c0001 | t0006 | g0208 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19074 | hp2 | a0002 | c0002 | t0008 | g0304 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19079 | hp2 | a0002 | c0002 | t0009 | g0041 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19080 | hp2 | a0002 | c0002 | t0008 | g0309 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19081 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19085 | hp2 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA19091 | hp2 | a0001 | c0001 | t0014 | g0177 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0050 | EUR | TSI | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0268 | SAS | GIH | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA20905 | hp2 | a0001 | c0001 | t0012 | g0255 | SAS | GIH | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0296 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0193 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02486 | hp2 | a0001 | c0001 | t0015 | g0281 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0172 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0288 | AFR | ACB | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | MSL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | MSL | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0167 | AFR | USA | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0253 | AFR | USA | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA20300 | hp1 | a0001 | c0001 | t0028 | g0198 | AFR | USA | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | USA | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0276 | AFR | LWK | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | LWK | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0123 | REF | REF | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0003 | REF | REF | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164908641
|
T | C | 1 | a0005 | 1 | HG00597.hp1 | missense_variant&splice_region_variant | MODERATE | c.1094A>G | p.Asn365Ser | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/12 | 1372/5750 | 1094/1389 | 365/462 | chr2 | 164908641 | ||
| chr2:164911670
|
A | C | 1 | a0006 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.929T>G | p.Leu310Trp | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/12 | 1207/5750 | 929/1389 | 310/462 | chr2 | 164911670 | ||
| chr2:164915139
|
A | G | 1 | a0004 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.823T>C | p.Tyr275His | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/12 | 1101/5750 | 823/1389 | 275/462 | chr2 | 164915139 | ||
| chr2:164937402
|
T | C | 1 | a0002 | 18 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(15): Show |
missense_variant | MODERATE | c.565A>G | p.Thr189Ala | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/12 | 843/5750 | 565/1389 | 189/462 | chr2 | 164937402 | ||
| chr2:164945602
|
G | A | 1 | a0003 | 3 | NA18986.hp1 NA18998.hp1 NA19066.hp1 |
missense_variant | MODERATE | c.355C>T | p.Pro119Ser | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 4/12 | 633/5750 | 355/1389 | 119/462 | chr2 | 164945602 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164898473
|
T | C | 1 | a0001c0003 | 14 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(11): Show |
synonymous_variant | LOW | c.1353A>G | p.Thr451Thr | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 1631/5750 | 1353/1389 | 451/462 | chr2 | 164898473 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164894489
|
A | G | 1 | a0001c0001t0020 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3948T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 3948 | chr2 | 164894489 | |||||
| chr2:164894666
|
G | A | 1 | a0001c0001t0035 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3771C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 3771 | chr2 | 164894666 | |||||
| chr2:164894677
|
G | A | 1 | a0001c0001t0021 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3760C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 3760 | chr2 | 164894677 | |||||
| chr2:164894804
|
A | G | 1 | a0001c0001t0029 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3633T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 3633 | chr2 | 164894804 | |||||
| chr2:164895019
|
T | A | 1 | a0001c0001t0029 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3418A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 3418 | chr2 | 164895019 | |||||
| chr2:164895091
|
G | T | 1 | a0001c0001t0032 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3346C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 3346 | chr2 | 164895091 | |||||
| chr2:164895304
|
A | G | 4 | a0001c0001t0004a0001c0001t0023a0001c0001t0025others(1): Show | 25 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3133T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 3133 | chr2 | 164895304 | |||||
| chr2:164895497
|
A | C | 11 | a0001c0001t0001a0001c0001t0010a0001c0001t0014others(8): Show | 128 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2940T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 2940 | chr2 | 164895497 | |||||
| chr2:164895671
|
C | A | 1 | a0001c0001t0015 | 2 | HG02486.hp2 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2766G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 2766 | chr2 | 164895671 | |||||
| chr2:164895894
|
CT | C | 1 | a0001c0001t0013 | 3 | HG02280.hp1 HG03486.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2542delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 2542 | chr2 | 164895894 | |||||
| chr2:164896006
|
G | C | 2 | a0001c0001t0022a0001c0001t0024 | 2 | HG01261.hp2 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2431C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 2431 | chr2 | 164896006 | |||||
| chr2:164896227
|
G | A | 4 | a0001c0001t0010a0001c0001t0022a0001c0001t0024others(1): Show | 7 | HG01261.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2210C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 2210 | chr2 | 164896227 | |||||
| chr2:164896294
|
AC | A | 7 | a0001c0001t0003a0001c0001t0004a0001c0001t0023others(4): Show | 82 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2142delG | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 2142 | chr2 | 164896294 | |||||
| chr2:164896386
|
A | G | 1 | a0001c0001t0027 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2051T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 2051 | chr2 | 164896386 | |||||
| chr2:164896388
|
A | T | 1 | a0001c0001t0028 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2049T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 2049 | chr2 | 164896388 | |||||
| chr2:164896539
|
T | C | 1 | a0001c0001t0034 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1898A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 1898 | chr2 | 164896539 | |||||
| chr2:164896603
|
G | C | 1 | a0001c0001t0030 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1834C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 1834 | chr2 | 164896603 | |||||
| chr2:164896608
|
A | G | 13 | a0001c0001t0001a0001c0001t0010a0001c0001t0012others(10): Show | 133 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*1829T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 1829 | chr2 | 164896608 | |||||
| chr2:164896652
|
A | G | 1 | a0001c0001t0016 | 2 | HG02258.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1785T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 1785 | chr2 | 164896652 | |||||
| chr2:164896766
|
G | A | 1 | a0002c0002t0031 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 1671 | chr2 | 164896766 | |||||
| chr2:164896904
|
C | T | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
3_prime_UTR_variant | MODIFIER | c.*1533G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 1533 | chr2 | 164896904 | |||||
| chr2:164896961
|
G | A | 1 | a0001c0001t0006 | 14 | NA18940.hp2 NA18951.hp1 NA18973.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1476C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 1476 | chr2 | 164896961 | |||||
| chr2:164896968
|
G | A | 2 | a0001c0001t0011a0001c0001t0027 | 5 | HG01106.hp2 HG01175.hp2 HG01358.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1469C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 1469 | chr2 | 164896968 | |||||
| chr2:164896991
|
G | T | 1 | a0001c0001t0027 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1446C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 1446 | chr2 | 164896991 | |||||
| chr2:164897166
|
C | T | 1 | a0001c0001t0033 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 1271 | chr2 | 164897166 | |||||
| chr2:164897253
|
G | C | 23 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(20): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*1184C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 1184 | chr2 | 164897253 | |||||
| chr2:164897530
|
T | A | 1 | a0002c0002t0009 | 6 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*907A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 907 | chr2 | 164897530 | |||||
| chr2:164897610
|
C | G | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*827G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 827 | chr2 | 164897610 | |||||
| chr2:164897748
|
TTTTTG | T | 1 | a0002c0002t0009 | 6 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*684_*688delCAAAA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 684 | chr2 | 164897748 | |||||
| chr2:164898066
|
A | AC | 11 | a0001c0001t0001a0001c0001t0010a0001c0001t0019others(8): Show | 127 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*370dupG | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 370 | chr2 | 164898066 | |||||
| chr2:164898101
|
A | T | 12 | a0001c0001t0001a0001c0001t0010a0001c0001t0014others(9): Show | 129 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*336T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 336 | chr2 | 164898101 | |||||
| chr2:164898328
|
A | G | 1 | a0001c0001t0018 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 109 | chr2 | 164898328 | |||||
| chr2:164898379
|
C | T | 1 | a0001c0001t0017 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*58G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 12/12 | 58 | chr2 | 164898379 | |||||
| chr2:164955355
|
C | A | 2 | a0002c0002t0008a0002c0002t0009 | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-108G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 1/12 | chr2 | 164955355 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164898967
|
C | T | 2 | a0001c0001t0016g0258a0001c0001t0016g0262 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1096-237G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164898967 | ||||||
| chr2:164899082
|
A | G | 16 | a0001c0001t0002g0095a0001c0001t0002g0291a0001c0001t0002g0292others(13): Show | 18 | HG01175.hp1 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1096-352T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164899082 | ||||||
| chr2:164899322
|
G | A | 3 | a0001c0001t0012g0036a0001c0001t0012g0255a0001c0001t0012g0257 | 4 | HG02145.hp2 HG02273.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-592C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164899322 | ||||||
| chr2:164899369
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1096-639G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164899369 | ||||||
| chr2:164899404
|
A | C | 1 | a0001c0001t0002g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1096-674T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164899404 | ||||||
| chr2:164899519
|
G | A | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-789C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164899519 | ||||||
| chr2:164899576
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1096-846G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164899576 | ||||||
| chr2:164899581
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1096-851C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164899581 | ||||||
| chr2:164899696
|
G | A | 1 | a0001c0003t0002g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1096-966C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164899696 | ||||||
| chr2:164900086
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1096-1356G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164900086 | ||||||
| chr2:164900109
|
G | T | 3 | a0002c0002t0008g0297a0002c0002t0008g0304a0002c0002t0008g0309 | 3 | NA18612.hp2 NA19074.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1096-1379C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164900109 | ||||||
| chr2:164900223
|
T | C | 299 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(296): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1096-1493A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164900223 | ||||||
| chr2:164900340
|
A | G | 226 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(223): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1096-1610T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164900340 | ||||||
| chr2:164900515
|
G | A | 1 | a0001c0001t0003g0013 | 2 | NA18970.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1096-1785C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164900515 | ||||||
| chr2:164900759
|
C | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG01168.hp2 HG01169.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1096-2029G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164900759 | ||||||
| chr2:164900764
|
C | T | 2 | a0001c0001t0028g0198a0005c0007t0004g0228 | 2 | HG00597.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1096-2034G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164900764 | ||||||
| chr2:164900861
|
C | CA | 73 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(70): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.1096-2132dupT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164900861 | ||||||
| chr2:164901175
|
C | A | 4 | a0001c0001t0007g0191a0001c0001t0007g0192a0001c0001t0007g0193others(1): Show | 4 | HG00735.hp2 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096-2445G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164901175 | ||||||
| chr2:164901297
|
C | T | 6 | a0001c0001t0002g0061a0001c0001t0002g0130a0001c0001t0002g0139others(3): Show | 6 | HG00673.hp1 HG01255.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096-2567G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164901297 | ||||||
| chr2:164901298
|
G | A | 1 | a0001c0001t0003g0197 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1096-2568C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164901298 | ||||||
| chr2:164901806
|
G | A | 1 | a0001c0001t0028g0198 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1096-3076C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164901806 | ||||||
| chr2:164901887
|
G | C | 1 | a0001c0001t0001g0226 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1096-3157C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164901887 | ||||||
| chr2:164902033
|
C | CT | 111 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(108): Show | 127 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1096-3304dupA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902033 | ||||||
| chr2:164902033
|
CT | C | 6 | a0001c0001t0002g0221a0001c0001t0002g0278a0001c0001t0007g0187others(3): Show | 6 | HG01167.hp1 HG01255.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1096-3304delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902033 | ||||||
| chr2:164902034
|
T | TC | 6 | a0001c0003t0002g0023a0001c0003t0002g0163a0001c0003t0002g0164others(3): Show | 7 | HG02723.hp2 HG02886.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096-3305_1096-330 others(5): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902034 | ||||||
| chr2:164902035
|
T | C | 11 | a0001c0001t0002g0095a0001c0001t0002g0291a0001c0001t0002g0292others(8): Show | 13 | HG01175.hp1 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1096-3305A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902035 | ||||||
| chr2:164902130
|
G | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0129 | 2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1096-3400C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902130 | ||||||
| chr2:164902163
|
A | G | 2 | a0001c0001t0016g0258a0001c0001t0016g0262 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1096-3433T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902163 | ||||||
| chr2:164902210
|
G | A | 1 | a0001c0001t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1096-3480C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902210 | ||||||
| chr2:164902291
|
G | A | 117 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 133 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1096-3561C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902291 | ||||||
| chr2:164902336
|
G | GT | 3 | a0001c0001t0010g0293a0001c0001t0010g0294a0001c0001t0010g0295 | 3 | HG02818.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1096-3607dupA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902336 | ||||||
| chr2:164902399
|
T | A | 71 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(68): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.1096-3669A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902399 | ||||||
| chr2:164902494
|
G | A | 1 | a0001c0001t0003g0053 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1096-3764C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902494 | ||||||
| chr2:164902535
|
C | T | 5 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(2): Show | 6 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096-3805G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902535 | ||||||
| chr2:164902959
|
A | G | 16 | a0001c0001t0002g0095a0001c0001t0002g0291a0001c0001t0002g0292others(13): Show | 18 | HG01175.hp1 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1096-4229T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902959 | ||||||
| chr2:164903198
|
G | GTC | 299 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(296): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1096-4469_1096-446 others(6): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164903198 | ||||||
| chr2:164904234
|
C | T | 2 | a0001c0001t0003g0053a0001c0001t0003g0060 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1095+4406G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164904234 | ||||||
| chr2:164904324
|
T | C | 1 | a0001c0001t0002g0061 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1095+4316A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164904324 | ||||||
| chr2:164904413
|
GA | G | 10 | a0001c0001t0006g0026a0001c0001t0006g0028a0001c0001t0006g0029others(7): Show | 13 | NA18940.hp2 NA18973.hp1 NA18975.hp2 others(10): Show |
intron_variant | MODIFIER | c.1095+4226delT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164904413 | ||||||
| chr2:164904466
|
A | G | 1 | a0001c0001t0033g0055 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1095+4174T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164904466 | ||||||
| chr2:164904471
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1095+4169A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164904471 | ||||||
| chr2:164904647
|
T | G | 207 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(204): Show | 243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1095+3993A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164904647 | ||||||
| chr2:164904850
|
A | G | 2 | a0001c0001t0015g0267a0001c0001t0015g0281 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1095+3790T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164904850 | ||||||
| chr2:164905049
|
G | T | 2 | a0001c0001t0015g0267a0001c0001t0015g0281 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1095+3591C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905049 | ||||||
| chr2:164905061
|
C | T | 68 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0010others(65): Show | 86 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1095+3579G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905061 | ||||||
| chr2:164905119
|
CT | C | 56 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(53): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1095+3520delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905119 | ||||||
| chr2:164905203
|
C | T | 1 | a0001c0001t0006g0211 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1095+3437G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905203 | ||||||
| chr2:164905241
|
C | A | 1 | a0001c0001t0003g0067 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1095+3399G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905241 | ||||||
| chr2:164905246
|
T | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0118 | 2 | NA19058.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1095+3394A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905246 | ||||||
| chr2:164905250
|
TG | T | 5 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(2): Show | 6 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+3389delC | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905250 | ||||||
| chr2:164905265
|
G | A | 117 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 133 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1095+3375C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905265 | ||||||
| chr2:164905293
|
C | G | 106 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(103): Show | 121 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1095+3347G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905293 | ||||||
| chr2:164905352
|
G | A | 1 | a0001c0001t0002g0236 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1095+3288C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905352 | ||||||
| chr2:164905429
|
G | A | 1 | a0001c0001t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1095+3211C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905429 | ||||||
| chr2:164905498
|
C | T | 1 | a0001c0001t0003g0074 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1095+3142G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905498 | ||||||
| chr2:164905499
|
G | A | 141 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(138): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1095+3141C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905499 | ||||||
| chr2:164905540
|
A | G | 1 | a0001c0001t0002g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1095+3100T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905540 | ||||||
| chr2:164906408
|
C | T | 2 | a0001c0001t0002g0048a0001c0001t0002g0201 | 2 | HG00280.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1095+2232G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164906408 | ||||||
| chr2:164906514
|
C | T | 6 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(3): Show | 7 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1095+2126G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164906514 | ||||||
| chr2:164906674
|
C | G | 1 | a0001c0001t0001g0155 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1095+1966G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164906674 | ||||||
| chr2:164906800
|
C | T | 1 | a0001c0001t0007g0290 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1095+1840G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164906800 | ||||||
| chr2:164906956
|
C | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0142a0001c0001t0001g0143others(17): Show | 23 | HG00408.hp1 HG02015.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1095+1684G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164906956 | ||||||
| chr2:164907247
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1095+1393G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907247 | ||||||
| chr2:164907270
|
C | CTTT | 17 | a0001c0001t0002g0291a0001c0001t0002g0292a0001c0001t0017g0220others(14): Show | 19 | HG01261.hp2 HG02280.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1095+1367_1095+136 others(7): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907270 | ||||||
| chr2:164907270
|
C | CTTTT | 21 | a0001c0001t0001g0064a0001c0001t0001g0121a0001c0001t0001g0122others(18): Show | 23 | HG00423.hp2 HG01175.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.1095+1366_1095+136 others(8): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907270 | ||||||
| chr2:164907270
|
C | CTTTTT | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(86): Show | 104 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1095+1365_1095+136 others(9): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907270 | ||||||
| chr2:164907270
|
C | CTTTTTT | 9 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0102others(6): Show | 9 | HG02056.hp2 HG02074.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.1095+1364_1095+136 others(10): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907270 | ||||||
| chr2:164907270
|
CT | C | 116 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(113): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1095+1369delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907270 | ||||||
| chr2:164907270
|
CTT | C | 14 | a0001c0001t0002g0056a0001c0001t0002g0098a0001c0001t0003g0066others(11): Show | 14 | HG00735.hp2 HG00738.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1095+1368_1095+136 others(6): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907270 | ||||||
| chr2:164907308
|
C | G | 5 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(2): Show | 6 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+1332G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907308 | ||||||
| chr2:164907348
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1095+1292T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907348 | ||||||
| chr2:164907407
|
G | A | 1 | a0001c0001t0003g0229 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1095+1233C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907407 | ||||||
| chr2:164907460
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1095+1180A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907460 | ||||||
| chr2:164907468
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1095+1172C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907468 | ||||||
| chr2:164907483
|
C | T | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1095+1157G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907483 | ||||||
| chr2:164907550
|
C | A | 1 | a0001c0001t0007g0290 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1095+1090G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907550 | ||||||
| chr2:164907638
|
T | C | 4 | a0001c0001t0012g0036a0001c0001t0012g0255a0001c0001t0012g0257others(1): Show | 5 | HG02145.hp2 HG02273.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.1095+1002A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907638 | ||||||
| chr2:164907927
|
T | A | 16 | a0001c0001t0002g0095a0001c0001t0002g0291a0001c0001t0002g0292others(13): Show | 18 | HG01175.hp1 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1095+713A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907927 | ||||||
| chr2:164907991
|
T | C | 2 | a0001c0001t0007g0187a0001c0001t0007g0188 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1095+649A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164907991 | ||||||
| chr2:164908232
|
T | G | 5 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(2): Show | 6 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+408A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164908232 | ||||||
| chr2:164908409
|
C | T | 1 | a0001c0001t0003g0074 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1095+231G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164908409 | ||||||
| chr2:164908631
|
C | T | 5 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(2): Show | 6 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+9G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164908631 | ||||||
| chr2:164909186
|
G | T | 7 | a0001c0001t0010g0293a0001c0001t0010g0294a0001c0001t0010g0295others(4): Show | 7 | HG01261.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.964-415C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164909186 | ||||||
| chr2:164909371
|
A | G | 1 | a0001c0001t0004g0044 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.964-600T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164909371 | ||||||
| chr2:164909472
|
C | T | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.964-701G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164909472 | ||||||
| chr2:164910078
|
AT | A | 10 | a0001c0001t0006g0026a0001c0001t0006g0028a0001c0001t0006g0029others(7): Show | 13 | NA18940.hp2 NA18973.hp1 NA18975.hp2 others(10): Show |
intron_variant | MODIFIER | c.964-1308delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164910078 | ||||||
| chr2:164910157
|
A | G | 1 | a0001c0001t0006g0207 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.964-1386T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164910157 | ||||||
| chr2:164910289
|
G | T | 1 | a0001c0001t0034g0261 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.963+1347C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164910289 | ||||||
| chr2:164910293
|
G | A | 1 | a0001c0001t0028g0198 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.963+1343C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164910293 | ||||||
| chr2:164910457
|
T | TA | 10 | a0001c0001t0006g0026a0001c0001t0006g0028a0001c0001t0006g0029others(7): Show | 13 | NA18940.hp2 NA18973.hp1 NA18975.hp2 others(10): Show |
intron_variant | MODIFIER | c.963+1178dupT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164910457 | ||||||
| chr2:164910596
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.963+1040G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164910596 | ||||||
| chr2:164910601
|
A | C | 1 | a0001c0001t0001g0260 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.963+1035T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164910601 | ||||||
| chr2:164910815
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.963+821G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164910815 | ||||||
| chr2:164911071
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0002g0271 | 2 | HG00642.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.963+565C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164911071 | ||||||
| chr2:164911274
|
A | C | 5 | a0001c0001t0011g0181a0001c0001t0011g0182a0001c0001t0011g0184others(2): Show | 5 | HG01106.hp2 HG01175.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+362T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164911274 | ||||||
| chr2:164911299
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.963+337T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164911299 | ||||||
| chr2:164911300
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.963+336C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164911300 | ||||||
| chr2:164911335
|
C | T | 5 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(2): Show | 6 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+301G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164911335 | ||||||
| chr2:164911428
|
C | T | 2 | a0001c0001t0007g0187a0001c0001t0007g0188 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.963+208G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164911428 | ||||||
| chr2:164911435
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.963+201A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164911435 | ||||||
| chr2:164911455
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.963+181G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164911455 | ||||||
| chr2:164911572
|
C | A | 1 | a0001c0001t0016g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.963+64G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 10/11 | chr2 | 164911572 | ||||||
| chr2:164911992
|
T | C | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.851-244A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164911992 | ||||||
| chr2:164912541
|
A | G | 208 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(205): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.851-793T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164912541 | ||||||
| chr2:164912674
|
C | G | 208 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(205): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.851-926G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164912674 | ||||||
| chr2:164912698
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.851-950C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164912698 | ||||||
| chr2:164912900
|
A | C | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.851-1152T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164912900 | ||||||
| chr2:164912901
|
A | G | 57 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(54): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.851-1153T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164912901 | ||||||
| chr2:164912937
|
A | T | 1 | a0001c0001t0002g0223 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.851-1189T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164912937 | ||||||
| chr2:164913022
|
T | G | 1 | a0001c0001t0004g0073 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.851-1274A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164913022 | ||||||
| chr2:164913169
|
T | A | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.851-1421A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164913169 | ||||||
| chr2:164913628
|
C | A | 7 | a0001c0001t0010g0293a0001c0001t0010g0294a0001c0001t0010g0295others(4): Show | 7 | HG01261.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+1484G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164913628 | ||||||
| chr2:164913669
|
G | GT | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.850+1442dupA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164913669 | ||||||
| chr2:164913696
|
A | C | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850+1416T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164913696 | ||||||
| chr2:164913947
|
A | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 135 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.850+1165T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164913947 | ||||||
| chr2:164914081
|
G | A | 1 | a0001c0001t0011g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.850+1031C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914081 | ||||||
| chr2:164914292
|
CCTGA | C | 15 | a0001c0001t0002g0095a0001c0001t0002g0291a0001c0001t0002g0292others(12): Show | 17 | HG01175.hp1 HG02280.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.850+816_850+819del others(4): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914292 | ||||||
| chr2:164914420
|
G | T | 25 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0015others(22): Show | 34 | HG00140.hp1 HG00673.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.850+692C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914420 | ||||||
| chr2:164914485
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.850+627C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914485 | ||||||
| chr2:164914609
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850+503C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914609 | ||||||
| chr2:164914610
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850+502A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914610 | ||||||
| chr2:164914611
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850+501C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914611 | ||||||
| chr2:164914612
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850+500C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914612 | ||||||
| chr2:164914616
|
G | C | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850+496C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914616 | ||||||
| chr2:164914618
|
A | C | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850+494T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914618 | ||||||
| chr2:164914626
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850+486C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914626 | ||||||
| chr2:164914627
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850+485C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914627 | ||||||
| chr2:164914628
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850+484C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914628 | ||||||
| chr2:164914752
|
A | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0120 | 3 | HG01070.hp2 HG01071.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.850+360T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914752 | ||||||
| chr2:164914879
|
A | G | 19 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0007g0187others(16): Show | 20 | HG00735.hp2 HG01496.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.850+233T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914879 | ||||||
| chr2:164914996
|
G | A | 15 | a0001c0001t0002g0095a0001c0001t0002g0291a0001c0001t0002g0292others(12): Show | 17 | HG01175.hp1 HG02280.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.850+116C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164914996 | ||||||
| chr2:164915060
|
G | A | 1 | a0001c0001t0001g0022 | 2 | HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.850+52C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164915060 | ||||||
| chr2:164915372
|
A | T | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.689-99T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 8/11 | chr2 | 164915372 | ||||||
| chr2:164915390
|
A | G | 1 | a0001c0003t0002g0163 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.689-117T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 8/11 | chr2 | 164915390 | ||||||
| chr2:164915510
|
A | C | 153 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(150): Show | 172 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.689-237T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 8/11 | chr2 | 164915510 | ||||||
| chr2:164915580
|
C | T | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.689-307G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 8/11 | chr2 | 164915580 | ||||||
| chr2:164915713
|
A | G | 1 | a0001c0001t0003g0186 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.688+190T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 8/11 | chr2 | 164915713 | ||||||
| chr2:164915861
|
G | T | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.688+42C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 8/11 | chr2 | 164915861 | ||||||
| chr2:164916062
|
A | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.618-89T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916062 | ||||||
| chr2:164916063
|
A | G | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.618-90T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916063 | ||||||
| chr2:164916066
|
G | T | 6 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(3): Show | 7 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-93C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916066 | ||||||
| chr2:164916094
|
G | A | 5 | a0001c0001t0003g0229a0001c0001t0003g0268a0001c0001t0003g0273others(2): Show | 5 | HG01192.hp2 HG01496.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.618-121C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916094 | ||||||
| chr2:164916311
|
G | A | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.618-338C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916311 | ||||||
| chr2:164916328
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.618-355A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916328 | ||||||
| chr2:164916388
|
A | C | 1 | a0001c0001t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.618-415T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916388 | ||||||
| chr2:164916406
|
A | C | 1 | a0001c0001t0012g0255 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.618-433T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916406 | ||||||
| chr2:164916612
|
T | C | 1 | a0001c0001t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.618-639A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916612 | ||||||
| chr2:164916758
|
G | T | 1 | a0001c0001t0003g0067 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.618-785C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916758 | ||||||
| chr2:164916902
|
A | C | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618-929T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916902 | ||||||
| chr2:164916903
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618-930C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916903 | ||||||
| chr2:164916904
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618-931A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916904 | ||||||
| chr2:164916907
|
C | G | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618-934G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916907 | ||||||
| chr2:164916909
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618-936C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916909 | ||||||
| chr2:164916910
|
G | C | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618-937C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916910 | ||||||
| chr2:164916911
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618-938T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916911 | ||||||
| chr2:164916912
|
C | T | 11 | a0001c0001t0002g0210a0001c0001t0006g0026a0001c0001t0006g0028others(8): Show | 14 | NA18940.hp2 NA18951.hp2 NA18973.hp1 others(11): Show |
intron_variant | MODIFIER | c.618-939G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916912 | ||||||
| chr2:164916913
|
C | G | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618-940G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916913 | ||||||
| chr2:164916915
|
C | G | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618-942G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916915 | ||||||
| chr2:164916917
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618-944G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916917 | ||||||
| chr2:164916929
|
T | A | 6 | a0001c0001t0007g0191a0001c0001t0007g0192a0001c0001t0007g0193others(3): Show | 6 | HG00735.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-956A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916929 | ||||||
| chr2:164916944
|
CTG | C | 4 | a0001c0001t0007g0191a0001c0001t0007g0192a0001c0001t0007g0193others(1): Show | 4 | HG00735.hp2 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-973_618-972del others(2): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164916944 | ||||||
| chr2:164917057
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 175 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.618-1084A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164917057 | ||||||
| chr2:164917058
|
A | G | 1 | a0001c0001t0012g0036 | 2 | HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.618-1085T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164917058 | ||||||
| chr2:164917183
|
G | A | 20 | a0001c0001t0002g0009a0001c0001t0002g0034a0001c0001t0002g0035others(17): Show | 27 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.618-1210C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164917183 | ||||||
| chr2:164917210
|
G | A | 215 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(212): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.618-1237C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164917210 | ||||||
| chr2:164917383
|
C | G | 1 | a0001c0003t0002g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.618-1410G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164917383 | ||||||
| chr2:164917425
|
A | G | 3 | a0001c0001t0006g0026a0001c0001t0006g0202a0001c0001t0006g0203 | 4 | NA18940.hp2 NA18986.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-1452T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164917425 | ||||||
| chr2:164917445
|
A | G | 47 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(44): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.618-1472T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164917445 | ||||||
| chr2:164917624
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.618-1651G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164917624 | ||||||
| chr2:164917638
|
T | C | 1 | a0001c0001t0034g0261 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.618-1665A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164917638 | ||||||
| chr2:164917717
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.618-1744G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164917717 | ||||||
| chr2:164917954
|
G | T | 2 | a0001c0001t0003g0076a0001c0001t0003g0127 | 2 | HG03654.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.618-1981C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164917954 | ||||||
| chr2:164918029
|
A | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.618-2056T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918029 | ||||||
| chr2:164918072
|
A | C | 11 | a0001c0001t0002g0210a0001c0001t0006g0026a0001c0001t0006g0028others(8): Show | 14 | NA18940.hp2 NA18951.hp2 NA18973.hp1 others(11): Show |
intron_variant | MODIFIER | c.618-2099T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918072 | ||||||
| chr2:164918099
|
G | C | 1 | a0001c0001t0003g0051 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.618-2126C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918099 | ||||||
| chr2:164918154
|
C | A | 1 | a0006c0006t0010g0254 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.618-2181G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918154 | ||||||
| chr2:164918258
|
A | G | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.618-2285T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918258 | ||||||
| chr2:164918304
|
T | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.618-2331A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918304 | ||||||
| chr2:164918307
|
A | G | 1 | a0002c0002t0031g0283 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.618-2334T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918307 | ||||||
| chr2:164918398
|
C | T | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.618-2425G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918398 | ||||||
| chr2:164918468
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.618-2495T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918468 | ||||||
| chr2:164918519
|
C | T | 43 | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0010others(40): Show | 58 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.618-2546G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918519 | ||||||
| chr2:164918577
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0133 | 2 | NA19081.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.618-2604T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918577 | ||||||
| chr2:164918581
|
G | A | 1 | a0001c0001t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.618-2608C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918581 | ||||||
| chr2:164918690
|
C | T | 282 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(279): Show | 336 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.618-2717G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918690 | ||||||
| chr2:164918704
|
T | C | 1 | a0001c0001t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.618-2731A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918704 | ||||||
| chr2:164918965
|
A | T | 19 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(16): Show | 21 | HG01175.hp1 HG02055.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.618-2992T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164918965 | ||||||
| chr2:164919017
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0213 | 5 | HG00140.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-3044G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919017 | ||||||
| chr2:164919065
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.618-3092C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919065 | ||||||
| chr2:164919142
|
C | A | 66 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0002g0002others(63): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.618-3169G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919142 | ||||||
| chr2:164919222
|
C | T | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.618-3249G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919222 | ||||||
| chr2:164919223
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 5 | HG01257.hp1 HG01981.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-3250C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919223 | ||||||
| chr2:164919267
|
C | G | 1 | a0001c0001t0002g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.618-3294G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919267 | ||||||
| chr2:164919318
|
C | A | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.618-3345G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919318 | ||||||
| chr2:164919319
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.618-3346C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919319 | ||||||
| chr2:164919368
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.618-3395C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919368 | ||||||
| chr2:164919474
|
A | G | 1 | a0001c0001t0003g0066 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.618-3501T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919474 | ||||||
| chr2:164919545
|
T | C | 1 | a0001c0001t0011g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.618-3572A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919545 | ||||||
| chr2:164919558
|
T | C | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.618-3585A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919558 | ||||||
| chr2:164919607
|
G | T | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.618-3634C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919607 | ||||||
| chr2:164919610
|
G | T | 1 | a0002c0002t0008g0299 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.618-3637C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919610 | ||||||
| chr2:164919667
|
T | C | 282 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(279): Show | 336 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.618-3694A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919667 | ||||||
| chr2:164919695
|
C | T | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.618-3722G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919695 | ||||||
| chr2:164919729
|
A | G | 116 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.618-3756T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919729 | ||||||
| chr2:164919766
|
A | G | 1 | a0001c0001t0016g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.618-3793T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919766 | ||||||
| chr2:164919853
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.618-3880C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919853 | ||||||
| chr2:164919878
|
G | A | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.618-3905C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919878 | ||||||
| chr2:164919899
|
C | G | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.618-3926G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919899 | ||||||
| chr2:164919996
|
A | G | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.618-4023T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164919996 | ||||||
| chr2:164920131
|
G | A | 4 | a0001c0001t0010g0293a0001c0001t0010g0294a0001c0001t0010g0295others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-4158C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920131 | ||||||
| chr2:164920138
|
G | A | 1 | a0002c0002t0008g0306 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.618-4165C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920138 | ||||||
| chr2:164920204
|
G | A | 1 | a0001c0001t0002g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.618-4231C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920204 | ||||||
| chr2:164920276
|
G | A | 4 | a0001c0001t0007g0191a0001c0001t0007g0192a0001c0001t0007g0193others(1): Show | 4 | HG00735.hp2 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-4303C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920276 | ||||||
| chr2:164920278
|
T | TA | 104 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(101): Show | 120 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.618-4306dupT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920278 | ||||||
| chr2:164920278
|
TA | T | 92 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(89): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.618-4306delT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920278 | ||||||
| chr2:164920378
|
A | G | 7 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(4): Show | 8 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.618-4405T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920378 | ||||||
| chr2:164920544
|
CCGA | C | 4 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-4574_618-4572d others(5): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920544 | ||||||
| chr2:164920545
|
CGAG | C | 188 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(185): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.618-4575_618-4573d others(5): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920545 | ||||||
| chr2:164920548
|
G | T | 4 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-4575C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920548 | ||||||
| chr2:164920558
|
C | G | 1 | a0001c0001t0016g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.618-4585G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920558 | ||||||
| chr2:164920581
|
C | A | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.618-4608G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920581 | ||||||
| chr2:164921012
|
T | C | 2 | a0001c0001t0003g0065a0001c0001t0003g0071 | 2 | NA18999.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.618-5039A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164921012 | ||||||
| chr2:164921199
|
G | A | 1 | a0002c0002t0031g0283 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.618-5226C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164921199 | ||||||
| chr2:164921215
|
G | A | 1 | a0001c0001t0002g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.618-5242C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164921215 | ||||||
| chr2:164921299
|
C | T | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.618-5326G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164921299 | ||||||
| chr2:164921362
|
A | G | 113 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(110): Show | 129 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.618-5389T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164921362 | ||||||
| chr2:164921373
|
A | T | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.618-5400T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164921373 | ||||||
| chr2:164921469
|
A | G | 5 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(2): Show | 6 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-5496T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164921469 | ||||||
| chr2:164921496
|
AT | A | 60 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(57): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.618-5524delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164921496 | ||||||
| chr2:164921550
|
T | G | 1 | a0001c0001t0022g0166 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.618-5577A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164921550 | ||||||
| chr2:164921701
|
A | G | 2 | a0001c0001t0007g0189a0001c0001t0007g0190 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.618-5728T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164921701 | ||||||
| chr2:164921890
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.618-5917A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164921890 | ||||||
| chr2:164922124
|
G | T | 5 | a0001c0001t0011g0181a0001c0001t0011g0182a0001c0001t0011g0184others(2): Show | 5 | HG01106.hp2 HG01175.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-6151C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164922124 | ||||||
| chr2:164922215
|
T | C | 17 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0032others(14): Show | 23 | HG00673.hp2 HG00738.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.618-6242A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164922215 | ||||||
| chr2:164922243
|
G | A | 9 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(6): Show | 10 | HG02145.hp2 HG02258.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-6270C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164922243 | ||||||
| chr2:164922272
|
G | A | 19 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(16): Show | 21 | HG01175.hp1 HG02055.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.618-6299C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164922272 | ||||||
| chr2:164922498
|
T | A | 215 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(212): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.618-6525A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164922498 | ||||||
| chr2:164922619
|
C | T | 4 | a0001c0001t0003g0229a0001c0001t0003g0273a0001c0001t0003g0274others(1): Show | 4 | HG01192.hp2 HG01496.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-6646G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164922619 | ||||||
| chr2:164922648
|
A | G | 9 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(6): Show | 10 | HG02145.hp2 HG02258.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-6675T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164922648 | ||||||
| chr2:164922668
|
TC | T | 4 | a0001c0001t0010g0293a0001c0001t0010g0294a0001c0001t0010g0295others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-6696delG | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164922668 | ||||||
| chr2:164922706
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.618-6733A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164922706 | ||||||
| chr2:164922739
|
A | G | 1 | a0001c0001t0021g0116 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.618-6766T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164922739 | ||||||
| chr2:164922777
|
A | G | 9 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(6): Show | 10 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-6804T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164922777 | ||||||
| chr2:164923423
|
C | T | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-7450G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164923423 | ||||||
| chr2:164923463
|
A | G | 1 | a0001c0001t0003g0275 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.618-7490T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164923463 | ||||||
| chr2:164923503
|
GC | G | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-7531delG | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164923503 | ||||||
| chr2:164923657
|
C | T | 1 | a0001c0001t0016g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.618-7684G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164923657 | ||||||
| chr2:164923658
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0029g0284 | 2 | HG02074.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.618-7685C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164923658 | ||||||
| chr2:164923673
|
T | C | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-7700A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164923673 | ||||||
| chr2:164923803
|
T | TA | 9 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(6): Show | 10 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-7831dupT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164923803 | ||||||
| chr2:164923803
|
TA | T | 19 | a0001c0001t0001g0148a0001c0001t0002g0095a0001c0001t0002g0096others(16): Show | 21 | HG01175.hp1 HG02280.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.618-7831delT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164923803 | ||||||
| chr2:164923855
|
A | G | 1 | a0001c0001t0016g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.618-7882T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164923855 | ||||||
| chr2:164923957
|
G | A | 1 | a0001c0003t0002g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.618-7984C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164923957 | ||||||
| chr2:164924038
|
C | A | 1 | a0001c0001t0004g0087 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.618-8065G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164924038 | ||||||
| chr2:164924090
|
A | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.618-8117T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164924090 | ||||||
| chr2:164924179
|
G | A | 3 | a0001c0001t0013g0251a0001c0001t0013g0252a0001c0001t0013g0253 | 3 | HG02280.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.618-8206C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164924179 | ||||||
| chr2:164924907
|
TG | T | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-8935delC | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164924907 | ||||||
| chr2:164924913
|
C | T | 15 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0032others(12): Show | 21 | HG00673.hp2 HG00738.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.618-8940G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164924913 | ||||||
| chr2:164924916
|
G | A | 1 | a0001c0001t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.618-8943C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164924916 | ||||||
| chr2:164924998
|
A | G | 215 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(212): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.618-9025T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164924998 | ||||||
| chr2:164925025
|
C | T | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-9052G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925025 | ||||||
| chr2:164925026
|
G | A | 1 | a0001c0001t0013g0253 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.618-9053C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925026 | ||||||
| chr2:164925147
|
T | C | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-9174A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925147 | ||||||
| chr2:164925179
|
G | A | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.618-9206C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925179 | ||||||
| chr2:164925213
|
G | A | 6 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(3): Show | 7 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-9240C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925213 | ||||||
| chr2:164925270
|
G | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(53): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.618-9297C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925270 | ||||||
| chr2:164925435
|
C | T | 282 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(279): Show | 336 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.618-9462G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925435 | ||||||
| chr2:164925492
|
T | TTG | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-9520_618-9519i others(4): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925492 | ||||||
| chr2:164925655
|
A | G | 1 | a0001c0001t0005g0136 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.618-9682T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925655 | ||||||
| chr2:164925662
|
A | T | 1 | a0001c0001t0016g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.618-9689T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925662 | ||||||
| chr2:164925665
|
T | C | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-9692A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925665 | ||||||
| chr2:164925668
|
G | C | 1 | a0001c0001t0003g0065 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.618-9695C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925668 | ||||||
| chr2:164925680
|
A | G | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.618-9707T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925680 | ||||||
| chr2:164925747
|
C | T | 1 | a0001c0001t0003g0079 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.618-9774G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925747 | ||||||
| chr2:164925915
|
C | T | 1 | a0001c0001t0017g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.618-9942G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164925915 | ||||||
| chr2:164926061
|
T | C | 57 | a0001c0001t0002g0050a0001c0001t0003g0001a0001c0001t0003g0004others(54): Show | 73 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.618-10088A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926061 | ||||||
| chr2:164926083
|
G | A | 18 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(15): Show | 20 | HG01175.hp1 HG02280.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.618-10110C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926083 | ||||||
| chr2:164926113
|
G | C | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-10140C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926113 | ||||||
| chr2:164926202
|
G | A | 2 | a0001c0001t0002g0048a0001c0001t0003g0072 | 2 | HG00280.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.618-10229C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926202 | ||||||
| chr2:164926340
|
C | T | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.618-10367G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926340 | ||||||
| chr2:164926358
|
T | C | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-10385A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926358 | ||||||
| chr2:164926401
|
TATAGCTT others(6): Show |
T | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.618-10441_618-1042 others(17): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926401 | ||||||
| chr2:164926506
|
C | A | 1 | a0001c0001t0002g0282 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.618-10533G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926506 | ||||||
| chr2:164926566
|
ATGTT | A | 4 | a0001c0001t0010g0293a0001c0001t0010g0294a0001c0001t0010g0295others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-10597_618-1059 others(8): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926566 | ||||||
| chr2:164926573
|
C | G | 4 | a0001c0001t0010g0293a0001c0001t0010g0294a0001c0001t0010g0295others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-10600G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926573 | ||||||
| chr2:164926703
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.617+10647C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926703 | ||||||
| chr2:164926722
|
A | T | 1 | a0002c0002t0008g0302 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.617+10628T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926722 | ||||||
| chr2:164926757
|
G | A | 6 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(3): Show | 7 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.617+10593C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926757 | ||||||
| chr2:164926801
|
G | A | 18 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(15): Show | 20 | HG01175.hp1 HG02280.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.617+10549C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926801 | ||||||
| chr2:164926924
|
A | G | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+10426T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926924 | ||||||
| chr2:164926926
|
T | C | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+10424A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926926 | ||||||
| chr2:164926927
|
G | A | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+10423C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926927 | ||||||
| chr2:164926937
|
C | A | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+10413G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926937 | ||||||
| chr2:164926945
|
T | C | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+10405A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926945 | ||||||
| chr2:164926946
|
G | A | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+10404C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926946 | ||||||
| chr2:164926959
|
A | C | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+10391T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926959 | ||||||
| chr2:164926967
|
C | A | 10 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(7): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+10383G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164926967 | ||||||
| chr2:164927126
|
C | T | 2 | a0001c0001t0004g0033a0001c0001t0023g0241 | 3 | NA18942.hp2 NA18968.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.617+10224G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164927126 | ||||||
| chr2:164927127
|
G | A | 105 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 120 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.617+10223C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164927127 | ||||||
| chr2:164927255
|
G | A | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.617+10095C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164927255 | ||||||
| chr2:164927404
|
A | T | 1 | a0001c0001t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.617+9946T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164927404 | ||||||
| chr2:164927510
|
A | G | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.617+9840T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164927510 | ||||||
| chr2:164927522
|
C | G | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.617+9828G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164927522 | ||||||
| chr2:164927629
|
C | G | 18 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(15): Show | 20 | HG01175.hp1 HG02280.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.617+9721G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164927629 | ||||||
| chr2:164927666
|
G | A | 9 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(6): Show | 10 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+9684C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164927666 | ||||||
| chr2:164927675
|
G | A | 1 | a0001c0001t0004g0200 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.617+9675C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164927675 | ||||||
| chr2:164927722
|
G | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(53): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.617+9628C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164927722 | ||||||
| chr2:164927756
|
C | T | 45 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(42): Show | 61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.617+9594G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164927756 | ||||||
| chr2:164927764
|
G | T | 45 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(42): Show | 61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.617+9586C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164927764 | ||||||
| chr2:164928067
|
C | T | 14 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(11): Show | 16 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.617+9283G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928067 | ||||||
| chr2:164928081
|
G | A | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.617+9269C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928081 | ||||||
| chr2:164928188
|
T | C | 1 | a0001c0001t0010g0296 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.617+9162A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928188 | ||||||
| chr2:164928206
|
C | A | 1 | a0001c0001t0002g0221 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.617+9144G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928206 | ||||||
| chr2:164928319
|
T | A | 1 | a0006c0006t0010g0254 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.617+9031A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928319 | ||||||
| chr2:164928345
|
C | A | 1 | a0001c0001t0003g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.617+9005G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928345 | ||||||
| chr2:164928634
|
C | T | 106 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(103): Show | 121 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.617+8716G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928634 | ||||||
| chr2:164928650
|
C | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0131a0001c0001t0001g0170 | 3 | HG00558.hp2 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.617+8700G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928650 | ||||||
| chr2:164928652
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.617+8698T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928652 | ||||||
| chr2:164928692
|
GGAAATTT others(9): Show |
G | 1 | a0001c0001t0002g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.617+8642_617+8657d others(18): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928692 | ||||||
| chr2:164928729
|
T | C | 1 | a0001c0001t0027g0180 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.617+8621A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928729 | ||||||
| chr2:164928742
|
C | T | 9 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(6): Show | 10 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+8608G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928742 | ||||||
| chr2:164928822
|
T | C | 2 | a0001c0001t0004g0062a0001c0001t0004g0073 | 2 | HG02074.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.617+8528A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928822 | ||||||
| chr2:164928841
|
A | C | 1 | a0002c0002t0031g0283 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.617+8509T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928841 | ||||||
| chr2:164928859
|
C | G | 1 | a0002c0002t0031g0283 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.617+8491G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928859 | ||||||
| chr2:164928896
|
C | G | 3 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0034g0261 | 3 | HG02572.hp2 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.617+8454G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164928896 | ||||||
| chr2:164929023
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.617+8327A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929023 | ||||||
| chr2:164929036
|
C | T | 4 | a0001c0001t0002g0095a0001c0001t0002g0291a0001c0001t0002g0292others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+8314G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929036 | ||||||
| chr2:164929076
|
A | G | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.617+8274T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929076 | ||||||
| chr2:164929329
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.617+8021C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929329 | ||||||
| chr2:164929540
|
T | G | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+7810A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929540 | ||||||
| chr2:164929542
|
C | T | 2 | a0001c0001t0003g0079a0001c0001t0003g0080 | 2 | NA18944.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.617+7808G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929542 | ||||||
| chr2:164929548
|
C | T | 1 | a0001c0001t0017g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.617+7802G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929548 | ||||||
| chr2:164929621
|
G | A | 1 | a0001c0001t0016g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.617+7729C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929621 | ||||||
| chr2:164929820
|
G | T | 151 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(148): Show | 180 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.617+7530C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929820 | ||||||
| chr2:164929823
|
T | C | 1 | a0001c0001t0024g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.617+7527A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929823 | ||||||
| chr2:164929884
|
AG | A | 13 | a0001c0001t0002g0048a0001c0001t0002g0050a0001c0001t0003g0014others(10): Show | 14 | HG00280.hp1 HG00738.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.617+7465delC | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929884 | ||||||
| chr2:164929897
|
C | A | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+7453G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929897 | ||||||
| chr2:164929931
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0246 | 2 | NA18949.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.617+7419T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929931 | ||||||
| chr2:164929968
|
C | T | 1 | a0001c0001t0005g0277 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.617+7382G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929968 | ||||||
| chr2:164929982
|
A | T | 6 | a0001c0001t0001g0143a0001c0001t0001g0225a0001c0001t0001g0226others(3): Show | 6 | HG02523.hp2 NA18944.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+7368T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164929982 | ||||||
| chr2:164930044
|
A | G | 1 | a0001c0001t0027g0180 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.617+7306T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930044 | ||||||
| chr2:164930144
|
A | C | 262 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.617+7206T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930144 | ||||||
| chr2:164930251
|
C | A | 1 | a0001c0001t0002g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.617+7099G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930251 | ||||||
| chr2:164930340
|
C | T | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+7010G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930340 | ||||||
| chr2:164930346
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.617+7004A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930346 | ||||||
| chr2:164930379
|
G | T | 20 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(17): Show | 22 | HG01175.hp1 HG01261.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.617+6971C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930379 | ||||||
| chr2:164930423
|
C | T | 2 | a0001c0001t0003g0076a0001c0001t0003g0127 | 2 | HG03654.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.617+6927G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930423 | ||||||
| chr2:164930475
|
T | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+6875A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930475 | ||||||
| chr2:164930483
|
G | T | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.617+6867C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930483 | ||||||
| chr2:164930528
|
C | A | 1 | a0001c0001t0016g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.617+6822G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930528 | ||||||
| chr2:164930625
|
C | A | 2 | a0003c0004t0001g0137a0003c0004t0001g0138 | 2 | NA18998.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.617+6725G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930625 | ||||||
| chr2:164930863
|
G | C | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 97 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.617+6487C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930863 | ||||||
| chr2:164930946
|
A | G | 271 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.617+6404T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930946 | ||||||
| chr2:164931163
|
C | G | 2 | a0001c0001t0015g0267a0001c0001t0032g0280 | 2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.617+6187G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931163 | ||||||
| chr2:164931169
|
G | A | 282 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(279): Show | 336 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.617+6181C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931169 | ||||||
| chr2:164931234
|
T | TC | 4 | a0001c0001t0012g0036a0001c0001t0012g0255a0001c0001t0016g0258others(1): Show | 5 | HG02258.hp1 HG02273.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.617+6115dupG | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931234 | ||||||
| chr2:164931234
|
T | TCC | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.617+6114_617+6115d others(4): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931234 | ||||||
| chr2:164931241
|
C | A | 4 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0257others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+6109G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931241 | ||||||
| chr2:164931241
|
C | CA | 16 | a0001c0001t0002g0095a0001c0001t0002g0265a0001c0001t0002g0272others(13): Show | 17 | HG01175.hp1 HG01175.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.617+6108dupT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931241 | ||||||
| chr2:164931241
|
C | CAA | 6 | a0001c0003t0002g0023a0001c0003t0002g0163a0001c0003t0002g0164others(3): Show | 7 | HG02723.hp2 HG02886.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+6107_617+6108d others(4): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931241 | ||||||
| chr2:164931241
|
CA | C | 196 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.617+6108delT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931241 | ||||||
| chr2:164931241
|
CAA | C | 8 | a0001c0001t0001g0108a0001c0001t0001g0118a0001c0001t0001g0158others(5): Show | 8 | HG01169.hp2 HG01433.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.617+6107_617+6108d others(4): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931241 | ||||||
| chr2:164931341
|
C | T | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.617+6009G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931341 | ||||||
| chr2:164931380
|
T | C | 1 | a0001c0001t0001g0215 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.617+5970A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931380 | ||||||
| chr2:164931505
|
C | G | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.617+5845G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931505 | ||||||
| chr2:164931721
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0133 | 2 | NA19081.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.617+5629G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931721 | ||||||
| chr2:164931773
|
C | G | 1 | a0001c0001t0034g0261 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.617+5577G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931773 | ||||||
| chr2:164931795
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.617+5555A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931795 | ||||||
| chr2:164931861
|
G | A | 1 | a0001c0001t0003g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.617+5489C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931861 | ||||||
| chr2:164931934
|
G | A | 1 | a0001c0001t0002g0050 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.617+5416C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931934 | ||||||
| chr2:164932002
|
G | A | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+5348C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164932002 | ||||||
| chr2:164932120
|
T | G | 1 | a0001c0001t0029g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.617+5230A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164932120 | ||||||
| chr2:164932129
|
G | A | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.617+5221C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164932129 | ||||||
| chr2:164932214
|
A | G | 20 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(17): Show | 22 | HG01175.hp1 HG01261.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.617+5136T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164932214 | ||||||
| chr2:164932228
|
A | G | 1 | a0001c0001t0011g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.617+5122T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164932228 | ||||||
| chr2:164932346
|
G | T | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.617+5004C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164932346 | ||||||
| chr2:164932391
|
C | T | 1 | a0002c0002t0031g0283 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.617+4959G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164932391 | ||||||
| chr2:164932627
|
T | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+4723A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164932627 | ||||||
| chr2:164932732
|
C | G | 2 | a0001c0001t0005g0287a0001c0001t0005g0288 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.617+4618G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164932732 | ||||||
| chr2:164932838
|
A | G | 1 | a0001c0001t0004g0199 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.617+4512T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164932838 | ||||||
| chr2:164932881
|
T | G | 1 | a0001c0001t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.617+4469A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164932881 | ||||||
| chr2:164932979
|
T | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+4371A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164932979 | ||||||
| chr2:164933039
|
T | C | 4 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(1): Show | 5 | HG00423.hp2 HG02523.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+4311A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933039 | ||||||
| chr2:164933142
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.617+4208T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933142 | ||||||
| chr2:164933161
|
A | G | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.617+4189T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933161 | ||||||
| chr2:164933245
|
G | GT | 20 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(17): Show | 22 | HG01175.hp1 HG01261.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.617+4104dupA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933245 | ||||||
| chr2:164933245
|
GT | G | 9 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(6): Show | 10 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+4104delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933245 | ||||||
| chr2:164933262
|
A | G | 1 | a0001c0001t0005g0286 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.617+4088T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933262 | ||||||
| chr2:164933310
|
T | C | 271 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.617+4040A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933310 | ||||||
| chr2:164933346
|
A | C | 17 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(14): Show | 18 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.617+4004T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933346 | ||||||
| chr2:164933390
|
A | T | 11 | a0001c0001t0002g0210a0001c0001t0006g0026a0001c0001t0006g0028others(8): Show | 14 | NA18940.hp2 NA18951.hp2 NA18973.hp1 others(11): Show |
intron_variant | MODIFIER | c.617+3960T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933390 | ||||||
| chr2:164933432
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0176 | 2 | HG01074.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.617+3918T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933432 | ||||||
| chr2:164933456
|
C | T | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+3894G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933456 | ||||||
| chr2:164933613
|
A | G | 4 | a0001c0001t0007g0191a0001c0001t0007g0192a0001c0001t0007g0193others(1): Show | 4 | HG00735.hp2 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+3737T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933613 | ||||||
| chr2:164933877
|
C | T | 1 | a0001c0001t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.617+3473G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933877 | ||||||
| chr2:164933891
|
C | T | 150 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(147): Show | 179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.617+3459G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164933891 | ||||||
| chr2:164934277
|
G | A | 4 | a0002c0002t0009g0041a0002c0002t0009g0298a0002c0002t0009g0300others(1): Show | 5 | HG00423.hp2 HG02523.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+3073C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164934277 | ||||||
| chr2:164934334
|
T | C | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.617+3016A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164934334 | ||||||
| chr2:164934348
|
A | G | 1 | a0001c0001t0021g0116 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.617+3002T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164934348 | ||||||
| chr2:164934357
|
G | T | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+2993C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164934357 | ||||||
| chr2:164934398
|
C | G | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+2952G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164934398 | ||||||
| chr2:164934401
|
A | C | 1 | a0001c0001t0004g0091 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.617+2949T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164934401 | ||||||
| chr2:164934647
|
C | T | 1 | a0001c0001t0002g0008 | 4 | HG02922.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+2703G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164934647 | ||||||
| chr2:164934716
|
C | G | 1 | a0001c0001t0002g0092 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.617+2634G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164934716 | ||||||
| chr2:164934828
|
T | C | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.617+2522A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164934828 | ||||||
| chr2:164934996
|
C | A | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.617+2354G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164934996 | ||||||
| chr2:164935097
|
C | T | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+2253G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164935097 | ||||||
| chr2:164935177
|
C | CT | 19 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(16): Show | 21 | HG01261.hp2 HG02280.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.617+2172dupA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164935177 | ||||||
| chr2:164935222
|
T | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+2128A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164935222 | ||||||
| chr2:164935226
|
G | A | 3 | a0001c0001t0003g0075a0001c0001t0003g0082a0001c0001t0003g0186 | 3 | NA18960.hp2 NA19063.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.617+2124C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164935226 | ||||||
| chr2:164935255
|
CCT | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+2093_617+2094d others(4): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164935255 | ||||||
| chr2:164935506
|
C | CA | 149 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(146): Show | 178 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.617+1843dupT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164935506 | ||||||
| chr2:164935506
|
CA | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+1843delT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164935506 | ||||||
| chr2:164935519
|
A | G | 1 | a0001c0001t0002g0035 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.617+1831T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164935519 | ||||||
| chr2:164935546
|
A | G | 272 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.617+1804T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164935546 | ||||||
| chr2:164935754
|
T | A | 1 | a0001c0001t0001g0128 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.617+1596A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164935754 | ||||||
| chr2:164935829
|
G | A | 65 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(62): Show | 86 | HG00099.hp2 HG00140.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.617+1521C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164935829 | ||||||
| chr2:164936032
|
T | C | 1 | a0001c0001t0003g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.617+1318A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164936032 | ||||||
| chr2:164936094
|
G | A | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.617+1256C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164936094 | ||||||
| chr2:164936207
|
G | A | 1 | a0001c0001t0003g0012 | 2 | NA18978.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.617+1143C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164936207 | ||||||
| chr2:164936257
|
T | G | 43 | a0001c0001t0001g0064a0001c0001t0003g0001a0001c0001t0003g0004others(40): Show | 58 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.617+1093A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164936257 | ||||||
| chr2:164936261
|
C | T | 272 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.617+1089G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164936261 | ||||||
| chr2:164936634
|
T | G | 1 | a0001c0001t0002g0264 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.617+716A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164936634 | ||||||
| chr2:164936764
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.617+586G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164936764 | ||||||
| chr2:164936808
|
G | A | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+542C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164936808 | ||||||
| chr2:164936838
|
CT | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.617+511delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164936838 | ||||||
| chr2:164936906
|
T | C | 1 | a0001c0001t0003g0076 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.617+444A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164936906 | ||||||
| chr2:164936943
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.617+407G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164936943 | ||||||
| chr2:164937051
|
C | T | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 97 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.617+299G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164937051 | ||||||
| chr2:164937068
|
A | C | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.617+282T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164937068 | ||||||
| chr2:164937072
|
A | G | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.617+278T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164937072 | ||||||
| chr2:164937254
|
A | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0106a0001c0001t0001g0115others(2): Show | 6 | HG00280.hp2 HG00642.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+96T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164937254 | ||||||
| chr2:164937458
|
G | A | 7 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(4): Show | 8 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.538-29C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164937458 | ||||||
| chr2:164937460
|
T | C | 1 | a0001c0001t0016g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.538-31A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164937460 | ||||||
| chr2:164937494
|
G | A | 1 | a0001c0001t0012g0257 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.538-65C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164937494 | ||||||
| chr2:164937499
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.538-70A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164937499 | ||||||
| chr2:164937527
|
A | G | 1 | a0001c0001t0002g0227 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.538-98T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164937527 | ||||||
| chr2:164937625
|
G | A | 1 | a0001c0001t0028g0198 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.538-196C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164937625 | ||||||
| chr2:164937798
|
C | T | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0246others(1): Show | 4 | NA18944.hp1 NA18949.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.538-369G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164937798 | ||||||
| chr2:164937967
|
C | T | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.538-538G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164937967 | ||||||
| chr2:164938084
|
C | T | 265 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(262): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.538-655G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164938084 | ||||||
| chr2:164938263
|
A | C | 1 | a0001c0001t0005g0287 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.538-834T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164938263 | ||||||
| chr2:164938292
|
C | A | 1 | a0001c0001t0003g0083 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.538-863G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164938292 | ||||||
| chr2:164938446
|
T | C | 1 | a0001c0001t0003g0077 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.537+1004A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164938446 | ||||||
| chr2:164938586
|
C | T | 19 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(16): Show | 21 | HG01175.hp1 HG01261.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.537+864G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164938586 | ||||||
| chr2:164938722
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.537+728A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164938722 | ||||||
| chr2:164938751
|
G | A | 257 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.537+699C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164938751 | ||||||
| chr2:164938755
|
G | A | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.537+695C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164938755 | ||||||
| chr2:164938784
|
A | T | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.537+666T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164938784 | ||||||
| chr2:164938790
|
A | G | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.537+660T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164938790 | ||||||
| chr2:164939117
|
C | T | 1 | a0001c0001t0016g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.537+333G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164939117 | ||||||
| chr2:164939118
|
C | T | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.537+332G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164939118 | ||||||
| chr2:164939217
|
T | G | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.537+233A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164939217 | ||||||
| chr2:164939218
|
G | A | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.537+232C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 6/11 | chr2 | 164939218 | ||||||
| chr2:164939698
|
A | G | 54 | a0001c0001t0001g0017a0001c0001t0001g0064a0001c0001t0002g0048others(51): Show | 71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.431-142T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164939698 | ||||||
| chr2:164939737
|
A | C | 1 | a0001c0001t0002g0247 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.431-181T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164939737 | ||||||
| chr2:164939738
|
AAC | A | 69 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(66): Show | 90 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.431-184_431-183del others(2): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164939738 | ||||||
| chr2:164939994
|
GT | G | 160 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.431-439delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164939994 | ||||||
| chr2:164939994
|
GTT | G | 6 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(3): Show | 6 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-440_431-439del others(2): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164939994 | ||||||
| chr2:164939994
|
GTTT | G | 68 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(65): Show | 89 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.431-441_431-439del others(3): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164939994 | ||||||
| chr2:164940110
|
C | G | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.431-554G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940110 | ||||||
| chr2:164940228
|
T | TTA | 5 | a0001c0001t0011g0181a0001c0001t0011g0182a0001c0001t0013g0251others(2): Show | 5 | HG01358.hp1 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-674_431-673dup others(2): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940228 | ||||||
| chr2:164940228
|
TTA | T | 17 | a0001c0001t0002g0030a0001c0001t0002g0039a0001c0001t0002g0265others(14): Show | 19 | HG00735.hp1 HG01109.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.431-674_431-673del others(2): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940228 | ||||||
| chr2:164940228
|
TTATA | T | 10 | a0001c0001t0002g0011a0001c0001t0002g0037a0001c0001t0002g0264others(7): Show | 14 | HG00099.hp1 HG00642.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.431-676_431-673del others(4): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940228 | ||||||
| chr2:164940228
|
TTATATAT others(1): Show |
T | 5 | a0001c0001t0002g0098a0001c0001t0002g0223a0001c0001t0003g0051others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-680_431-673del others(8): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940228 | ||||||
| chr2:164940228
|
TTATATAT others(3): Show |
T | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.431-682_431-673del others(10): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940228 | ||||||
| chr2:164940228
|
TTATATAT others(5): Show |
T | 15 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0003g0046others(12): Show | 18 | HG01261.hp1 HG02055.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.431-684_431-673del others(12): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940228 | ||||||
| chr2:164940274
|
T | C | 1 | a0001c0001t0002g0213 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.431-718A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940274 | ||||||
| chr2:164940406
|
C | A | 5 | a0001c0001t0004g0025a0001c0001t0004g0033a0001c0001t0004g0199others(2): Show | 7 | HG00621.hp2 NA18612.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-850G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940406 | ||||||
| chr2:164940470
|
C | T | 1 | a0001c0001t0010g0296 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.431-914G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940470 | ||||||
| chr2:164940471
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.431-915C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940471 | ||||||
| chr2:164940600
|
A | G | 257 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.431-1044T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940600 | ||||||
| chr2:164940631
|
A | T | 11 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(8): Show | 11 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.431-1075T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940631 | ||||||
| chr2:164940669
|
T | C | 1 | a0001c0001t0003g0243 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.431-1113A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940669 | ||||||
| chr2:164940716
|
T | C | 1 | a0001c0001t0018g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.431-1160A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940716 | ||||||
| chr2:164940750
|
G | GTA | 18 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0007g0187others(15): Show | 19 | HG00735.hp2 HG01496.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.431-1196_431-1195d others(4): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164940750 | ||||||
| chr2:164941001
|
A | G | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-1445T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164941001 | ||||||
| chr2:164941194
|
C | T | 1 | a0001c0001t0002g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.431-1638G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164941194 | ||||||
| chr2:164941219
|
A | G | 1 | a0001c0001t0025g0088 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.431-1663T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164941219 | ||||||
| chr2:164941656
|
G | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0176a0001c0001t0003g0078 | 3 | HG01074.hp2 HG02071.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.431-2100C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164941656 | ||||||
| chr2:164941691
|
T | C | 1 | a0001c0001t0002g0223 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431-2135A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164941691 | ||||||
| chr2:164941811
|
C | T | 7 | a0001c0001t0002g0217a0001c0001t0003g0268a0001c0001t0011g0181others(4): Show | 7 | HG01106.hp1 HG01106.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-2255G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164941811 | ||||||
| chr2:164942006
|
G | A | 1 | a0001c0001t0016g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.431-2450C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942006 | ||||||
| chr2:164942049
|
C | T | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-2493G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942049 | ||||||
| chr2:164942059
|
C | T | 12 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0006g0026others(9): Show | 15 | HG02055.hp2 NA18940.hp2 NA18951.hp2 others(12): Show |
intron_variant | MODIFIER | c.431-2503G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942059 | ||||||
| chr2:164942064
|
T | C | 4 | a0001c0001t0011g0181a0001c0001t0011g0182a0001c0001t0011g0184others(1): Show | 4 | HG01175.hp2 HG01358.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+2505A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942064 | ||||||
| chr2:164942091
|
C | T | 5 | a0001c0001t0011g0181a0001c0001t0011g0182a0001c0001t0011g0184others(2): Show | 5 | HG01106.hp2 HG01175.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+2478G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942091 | ||||||
| chr2:164942117
|
G | A | 19 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(16): Show | 21 | HG01175.hp1 HG01261.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.430+2452C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942117 | ||||||
| chr2:164942145
|
T | A | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+2424A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942145 | ||||||
| chr2:164942205
|
T | G | 2 | a0001c0001t0003g0079a0001c0001t0003g0080 | 2 | NA18944.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.430+2364A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942205 | ||||||
| chr2:164942247
|
G | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+2322C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942247 | ||||||
| chr2:164942309
|
C | T | 19 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(16): Show | 21 | HG01175.hp1 HG01261.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.430+2260G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942309 | ||||||
| chr2:164942353
|
T | G | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+2216A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942353 | ||||||
| chr2:164942432
|
C | CA | 168 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(165): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.430+2136dupT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942432 | ||||||
| chr2:164942432
|
C | CAA | 22 | a0001c0001t0001g0131a0001c0001t0001g0155a0001c0001t0002g0061others(19): Show | 22 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+2135_430+2136d others(4): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942432 | ||||||
| chr2:164942432
|
C | CAAA | 6 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(3): Show | 7 | HG02258.hp1 HG02273.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+2134_430+2136d others(5): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942432 | ||||||
| chr2:164942448
|
C | A | 1 | a0001c0001t0001g0263 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.430+2121G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942448 | ||||||
| chr2:164942579
|
T | C | 4 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+1990A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942579 | ||||||
| chr2:164942613
|
C | A | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+1956G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942613 | ||||||
| chr2:164942690
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.430+1879C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942690 | ||||||
| chr2:164942759
|
G | A | 1 | a0001c0001t0003g0082 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.430+1810C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942759 | ||||||
| chr2:164942798
|
C | T | 58 | a0001c0001t0001g0017a0001c0001t0001g0064a0001c0001t0002g0048others(55): Show | 75 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.430+1771G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942798 | ||||||
| chr2:164942994
|
T | G | 1 | a0001c0001t0010g0296 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.430+1575A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942994 | ||||||
| chr2:164943213
|
A | C | 1 | a0001c0001t0028g0198 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.430+1356T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164943213 | ||||||
| chr2:164943334
|
C | T | 16 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(13): Show | 18 | HG01261.hp2 HG02280.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.430+1235G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164943334 | ||||||
| chr2:164943423
|
C | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0063a0001c0001t0001g0110others(8): Show | 14 | HG00438.hp1 HG00673.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.430+1146G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164943423 | ||||||
| chr2:164943439
|
T | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+1130A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164943439 | ||||||
| chr2:164943474
|
A | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+1095T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164943474 | ||||||
| chr2:164943516
|
T | C | 1 | a0001c0001t0002g0034 | 2 | HG01361.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.430+1053A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164943516 | ||||||
| chr2:164943679
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.430+890T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164943679 | ||||||
| chr2:164944343
|
T | A | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+226A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164944343 | ||||||
| chr2:164944514
|
A | G | 1 | a0001c0001t0019g0224 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.430+55T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164944514 | ||||||
| chr2:164944694
|
T | C | 1 | a0001c0001t0003g0083 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.365-60A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 4/11 | chr2 | 164944694 | ||||||
| chr2:164944830
|
A | T | 12 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0006g0026others(9): Show | 15 | HG02055.hp2 NA18940.hp2 NA18951.hp2 others(12): Show |
intron_variant | MODIFIER | c.365-196T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 4/11 | chr2 | 164944830 | ||||||
| chr2:164944849
|
C | T | 147 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(144): Show | 176 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.365-215G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 4/11 | chr2 | 164944849 | ||||||
| chr2:164944871
|
C | A | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.365-237G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 4/11 | chr2 | 164944871 | ||||||
| chr2:164945162
|
A | G | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.364+431T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 4/11 | chr2 | 164945162 | ||||||
| chr2:164945255
|
C | CT | 70 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(67): Show | 83 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.364+337dupA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 4/11 | chr2 | 164945255 | ||||||
| chr2:164945255
|
CT | C | 31 | a0001c0001t0001g0205a0001c0001t0001g0259a0001c0001t0001g0263others(28): Show | 35 | HG01167.hp1 HG01175.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.364+337delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 4/11 | chr2 | 164945255 | ||||||
| chr2:164945359
|
C | T | 1 | a0001c0001t0007g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.364+234G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 4/11 | chr2 | 164945359 | ||||||
| chr2:164945372
|
T | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.364+221A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 4/11 | chr2 | 164945372 | ||||||
| chr2:164945752
|
G | T | 1 | a0002c0002t0008g0307 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.230-25C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164945752 | ||||||
| chr2:164945886
|
A | G | 1 | a0001c0001t0003g0065 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.230-159T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164945886 | ||||||
| chr2:164945995
|
C | T | 55 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(52): Show | 73 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.230-268G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164945995 | ||||||
| chr2:164946071
|
T | G | 1 | a0001c0001t0002g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.230-344A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946071 | ||||||
| chr2:164946106
|
C | A | 1 | a0001c0001t0002g0245 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.230-379G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946106 | ||||||
| chr2:164946254
|
CTA | C | 244 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.230-529_230-528del others(2): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946254 | ||||||
| chr2:164946305
|
C | T | 5 | a0001c0001t0011g0181a0001c0001t0011g0182a0001c0001t0011g0184others(2): Show | 5 | HG01106.hp2 HG01175.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-578G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946305 | ||||||
| chr2:164946308
|
T | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(5): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.230-581A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946308 | ||||||
| chr2:164946523
|
G | C | 104 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(101): Show | 128 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.230-796C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946523 | ||||||
| chr2:164946539
|
T | C | 30 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(27): Show | 32 | HG00735.hp2 HG01175.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.230-812A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946539 | ||||||
| chr2:164946564
|
C | CA | 78 | a0001c0001t0001g0017a0001c0001t0001g0259a0001c0001t0001g0263others(75): Show | 95 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.230-838dupT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946564 | ||||||
| chr2:164946564
|
C | CAA | 6 | a0001c0001t0003g0084a0001c0001t0003g0093a0001c0001t0004g0044others(3): Show | 6 | HG01175.hp2 HG02074.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.230-839_230-838dup others(2): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946564 | ||||||
| chr2:164946564
|
CA | C | 132 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.230-838delT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946564 | ||||||
| chr2:164946564
|
CAA | C | 7 | a0001c0001t0001g0113a0001c0001t0002g0008a0001c0001t0002g0054others(4): Show | 10 | HG00140.hp1 HG01167.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-839_230-838del others(2): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946564 | ||||||
| chr2:164946589
|
G | A | 69 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(66): Show | 90 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.230-862C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946589 | ||||||
| chr2:164946680
|
T | C | 1 | a0001c0001t0015g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.230-953A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946680 | ||||||
| chr2:164946781
|
A | G | 1 | a0001c0001t0006g0202 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.230-1054T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946781 | ||||||
| chr2:164946792
|
T | C | 55 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(52): Show | 73 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.230-1065A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946792 | ||||||
| chr2:164946825
|
T | C | 57 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(54): Show | 75 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.230-1098A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946825 | ||||||
| chr2:164946839
|
T | A | 19 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(16): Show | 21 | HG01175.hp1 HG01261.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.230-1112A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946839 | ||||||
| chr2:164946880
|
T | A | 185 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(182): Show | 217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.230-1153A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946880 | ||||||
| chr2:164946880
|
T | G | 85 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(82): Show | 107 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.230-1153A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946880 | ||||||
| chr2:164946893
|
T | C | 10 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0054others(7): Show | 15 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.230-1166A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946893 | ||||||
| chr2:164946909
|
T | C | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.230-1182A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946909 | ||||||
| chr2:164946927
|
A | G | 7 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(4): Show | 7 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.230-1200T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946927 | ||||||
| chr2:164947026
|
T | C | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.230-1299A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947026 | ||||||
| chr2:164947070
|
G | C | 1 | a0001c0001t0011g0182 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.230-1343C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947070 | ||||||
| chr2:164947087
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.230-1360G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947087 | ||||||
| chr2:164947117
|
C | CT | 9 | a0001c0001t0002g0037a0001c0001t0002g0264a0001c0001t0002g0265others(6): Show | 12 | HG00099.hp1 HG00423.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.230-1391dupA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
C | CTTTTTTT | 6 | a0001c0001t0007g0187a0001c0001t0007g0189a0001c0001t0007g0191others(3): Show | 6 | HG00735.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.230-1397_230-1391d others(9): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
C | CTTTTTTT others(1): Show |
6 | a0001c0001t0002g0095a0001c0001t0002g0098a0001c0001t0022g0166others(3): Show | 6 | HG01175.hp1 HG01261.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.230-1398_230-1391d others(10): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
C | CTTTTTTT others(2): Show |
8 | a0001c0001t0002g0097a0001c0001t0024g0175a0001c0003t0002g0023others(5): Show | 9 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.230-1399_230-1391d others(11): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
C | CTTTTTTT others(3): Show |
1 | a0001c0003t0002g0024 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.230-1400_230-1391d others(12): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.230-1402_230-1391d others(14): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.230-1405_230-1391d others(17): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
CT | C | 21 | a0001c0001t0002g0061a0001c0001t0002g0282a0001c0001t0003g0004others(18): Show | 24 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.230-1391delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
CTT | C | 61 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0064others(58): Show | 73 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.230-1392_230-1391d others(4): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
CTTT | C | 67 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(64): Show | 79 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.230-1393_230-1391d others(5): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
CTTTT | C | 23 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0100others(20): Show | 26 | HG00140.hp2 HG00408.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.230-1394_230-1391d others(6): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0007g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.230-1400_230-1391d others(12): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
CTTTTTTT others(7): Show |
C | 1 | a0003c0004t0001g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.230-1404_230-1391d others(16): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0002g0030a0001c0001t0002g0217a0001c0001t0026g0218others(1): Show | 5 | HG01106.hp1 HG01109.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.230-1406_230-1391d others(18): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947117
|
CTTTTTTT others(13): Show |
C | 68 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(65): Show | 89 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.230-1410_230-1391d others(22): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947117 | ||||||
| chr2:164947122
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.230-1395A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947122 | ||||||
| chr2:164947170
|
C | T | 1 | a0001c0001t0028g0198 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.230-1443G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947170 | ||||||
| chr2:164947188
|
G | C | 5 | a0001c0001t0005g0040a0001c0001t0005g0286a0001c0001t0005g0287others(2): Show | 6 | HG02559.hp2 HG02615.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.230-1461C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947188 | ||||||
| chr2:164947217
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | NA18978.hp2 NA18985.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.230-1490G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947217 | ||||||
| chr2:164947304
|
G | T | 11 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(8): Show | 11 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.230-1577C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947304 | ||||||
| chr2:164947351
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.230-1624G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947351 | ||||||
| chr2:164947407
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0213 | 5 | HG00140.hp1 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-1680G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947407 | ||||||
| chr2:164947422
|
G | A | 75 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0064others(72): Show | 93 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.230-1695C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947422 | ||||||
| chr2:164947458
|
A | G | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.230-1731T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947458 | ||||||
| chr2:164947465
|
T | G | 75 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0064others(72): Show | 93 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.230-1738A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947465 | ||||||
| chr2:164947519
|
T | G | 8 | a0001c0001t0001g0022a0001c0001t0001g0159a0001c0001t0001g0160others(5): Show | 9 | HG01257.hp1 HG01981.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.230-1792A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947519 | ||||||
| chr2:164947653
|
A | T | 1 | a0001c0001t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.230-1926T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947653 | ||||||
| chr2:164947779
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.230-2052T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947779 | ||||||
| chr2:164947917
|
C | A | 16 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(13): Show | 18 | HG01261.hp2 HG02280.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.230-2190G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164947917 | ||||||
| chr2:164948068
|
A | C | 273 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.230-2341T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948068 | ||||||
| chr2:164948137
|
G | A | 1 | a0001c0001t0004g0091 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.230-2410C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948137 | ||||||
| chr2:164948149
|
C | A | 64 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(61): Show | 81 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.230-2422G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948149 | ||||||
| chr2:164948150
|
C | T | 179 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.230-2423G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948150 | ||||||
| chr2:164948213
|
A | C | 4 | a0001c0001t0007g0191a0001c0001t0007g0192a0001c0001t0007g0193others(1): Show | 4 | HG00735.hp2 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-2486T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948213 | ||||||
| chr2:164948481
|
A | T | 273 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.230-2754T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948481 | ||||||
| chr2:164948545
|
T | C | 163 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(160): Show | 199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.230-2818A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948545 | ||||||
| chr2:164948570
|
A | G | 273 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.230-2843T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948570 | ||||||
| chr2:164948680
|
C | T | 1 | a0001c0001t0016g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.230-2953G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948680 | ||||||
| chr2:164948726
|
T | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | NA18963.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.230-2999A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948726 | ||||||
| chr2:164948878
|
T | C | 2 | a0001c0001t0007g0189a0001c0001t0007g0190 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.230-3151A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948878 | ||||||
| chr2:164948888
|
C | CT | 22 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0006g0026others(19): Show | 24 | HG00735.hp2 HG01496.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.230-3162dupA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948888 | ||||||
| chr2:164948888
|
C | CTT | 9 | a0001c0001t0001g0263a0001c0001t0006g0028a0001c0001t0006g0207others(6): Show | 10 | HG01106.hp2 HG01175.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-3163_230-3162d others(4): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948888 | ||||||
| chr2:164948888
|
C | CTTT | 12 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0006g0206others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.230-3164_230-3162d others(5): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948888 | ||||||
| chr2:164948888
|
CT | C | 10 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0002g0201others(7): Show | 11 | HG00558.hp2 HG01070.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.230-3162delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948888 | ||||||
| chr2:164948905
|
T | C | 112 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 127 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.230-3178A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948905 | ||||||
| chr2:164948905
|
T | TC | 66 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0064others(63): Show | 88 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.230-3179dupG | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948905 | ||||||
| chr2:164948933
|
C | A | 1 | a0001c0001t0007g0290 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.230-3206G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948933 | ||||||
| chr2:164949194
|
AAT | A | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 247 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.230-3469_230-3468d others(4): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949194 | ||||||
| chr2:164949197
|
T | G | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 247 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.230-3470A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949197 | ||||||
| chr2:164949230
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.229+3477A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949230 | ||||||
| chr2:164949232
|
T | A | 1 | a0002c0002t0008g0308 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.229+3475A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949232 | ||||||
| chr2:164949317
|
C | T | 7 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0012g0036others(4): Show | 8 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.229+3390G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949317 | ||||||
| chr2:164949370
|
G | A | 1 | a0001c0001t0024g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.229+3337C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949370 | ||||||
| chr2:164949404
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0204a0001c0001t0001g0205 | 4 | HG02132.hp1 HG02165.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+3303G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949404 | ||||||
| chr2:164949405
|
A | G | 273 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.229+3302T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949405 | ||||||
| chr2:164949411
|
C | T | 3 | a0001c0001t0006g0026a0001c0001t0006g0202a0001c0001t0006g0203 | 4 | NA18940.hp2 NA18986.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+3296G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949411 | ||||||
| chr2:164949466
|
C | T | 19 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0263others(16): Show | 20 | HG01106.hp2 HG01175.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.229+3241G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949466 | ||||||
| chr2:164949544
|
C | T | 1 | a0001c0001t0014g0177 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.229+3163G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949544 | ||||||
| chr2:164949805
|
T | G | 1 | a0001c0001t0007g0290 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.229+2902A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949805 | ||||||
| chr2:164949899
|
A | T | 19 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0263others(16): Show | 20 | HG01106.hp2 HG01175.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.229+2808T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949899 | ||||||
| chr2:164949952
|
A | ATTGTGGA others(2): Show |
9 | a0001c0001t0002g0048a0001c0001t0002g0050a0001c0001t0003g0014others(6): Show | 10 | HG00280.hp1 HG00738.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.229+2746_229+2754d others(11): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164949952 | ||||||
| chr2:164950185
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.229+2522C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164950185 | ||||||
| chr2:164950354
|
A | G | 3 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098 | 3 | HG02451.hp2 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.229+2353T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164950354 | ||||||
| chr2:164950455
|
T | C | 179 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.229+2252A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164950455 | ||||||
| chr2:164950596
|
C | T | 3 | a0001c0001t0013g0251a0001c0001t0013g0252a0001c0001t0013g0253 | 3 | HG02280.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.229+2111G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164950596 | ||||||
| chr2:164950622
|
A | C | 2 | a0001c0001t0002g0291a0001c0001t0002g0292 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.229+2085T>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164950622 | ||||||
| chr2:164950678
|
T | C | 1 | a0001c0001t0003g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.229+2029A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164950678 | ||||||
| chr2:164950711
|
T | C | 1 | a0001c0001t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.229+1996A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164950711 | ||||||
| chr2:164950743
|
T | C | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 236 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.229+1964A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164950743 | ||||||
| chr2:164950958
|
A | G | 1 | a0001c0001t0002g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.229+1749T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164950958 | ||||||
| chr2:164950969
|
CTTTATTT | C | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.229+1731_229+1737d others(9): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164950969 | ||||||
| chr2:164951048
|
G | T | 179 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.229+1659C>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951048 | ||||||
| chr2:164951054
|
T | C | 1 | a0001c0001t0002g0035 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.229+1653A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951054 | ||||||
| chr2:164951145
|
T | C | 1 | a0002c0002t0008g0309 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.229+1562A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951145 | ||||||
| chr2:164951152
|
C | T | 179 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.229+1555G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951152 | ||||||
| chr2:164951207
|
C | T | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 236 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.229+1500G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951207 | ||||||
| chr2:164951216
|
GT | G | 11 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(8): Show | 11 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.229+1490delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951216 | ||||||
| chr2:164951263
|
TTAAA | T | 5 | a0001c0001t0011g0181a0001c0001t0011g0182a0001c0001t0011g0184others(2): Show | 5 | HG01106.hp2 HG01175.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+1440_229+1443d others(6): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951263 | ||||||
| chr2:164951271
|
A | T | 64 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(61): Show | 81 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.229+1436T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951271 | ||||||
| chr2:164951361
|
A | T | 64 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(61): Show | 81 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.229+1346T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951361 | ||||||
| chr2:164951363
|
T | A | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.229+1344A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951363 | ||||||
| chr2:164951519
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.229+1188C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951519 | ||||||
| chr2:164951547
|
G | A | 66 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0064others(63): Show | 88 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.229+1160C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951547 | ||||||
| chr2:164951598
|
G | C | 179 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.229+1109C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951598 | ||||||
| chr2:164951701
|
A | G | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.229+1006T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951701 | ||||||
| chr2:164951730
|
G | A | 179 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.229+977C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951730 | ||||||
| chr2:164951752
|
G | A | 11 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(8): Show | 11 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.229+955C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951752 | ||||||
| chr2:164951833
|
T | C | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0014g0177 | 3 | HG02071.hp1 NA19000.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.229+874A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951833 | ||||||
| chr2:164951841
|
C | T | 1 | a0001c0001t0002g0008 | 4 | HG02922.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+866G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951841 | ||||||
| chr2:164951940
|
C | T | 4 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+767G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951940 | ||||||
| chr2:164951983
|
GCCA | G | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 247 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.229+721_229+723del others(3): Show |
SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951983 | ||||||
| chr2:164952136
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.229+571G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164952136 | ||||||
| chr2:164952192
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.229+515A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164952192 | ||||||
| chr2:164952268
|
G | A | 163 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(160): Show | 199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.229+439C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164952268 | ||||||
| chr2:164952476
|
G | A | 1 | a0001c0001t0002g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.229+231C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164952476 | ||||||
| chr2:164952556
|
C | T | 1 | a0001c0001t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.229+151G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164952556 | ||||||
| chr2:164952628
|
A | ATG | 23 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0263others(20): Show | 25 | HG00621.hp2 HG01106.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.229+77_229+78dupCA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164952628 | ||||||
| chr2:164952628
|
ATG | A | 112 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 127 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.229+77_229+78delCA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164952628 | ||||||
| chr2:164952916
|
T | C | 64 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(61): Show | 81 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.155-135A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164952916 | ||||||
| chr2:164952925
|
A | T | 4 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0004g0043others(1): Show | 7 | HG00597.hp2 HG02273.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-144T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164952925 | ||||||
| chr2:164953070
|
A | T | 163 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(160): Show | 199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.155-289T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164953070 | ||||||
| chr2:164953075
|
T | G | 1 | a0001c0001t0002g0249 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.155-294A>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164953075 | ||||||
| chr2:164953149
|
C | T | 4 | a0001c0001t0013g0251a0001c0001t0013g0252a0001c0001t0013g0253others(1): Show | 4 | HG02280.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-368G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164953149 | ||||||
| chr2:164953357
|
A | G | 66 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0064others(63): Show | 88 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.155-576T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164953357 | ||||||
| chr2:164953373
|
C | T | 11 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(8): Show | 11 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-592G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164953373 | ||||||
| chr2:164953383
|
G | A | 179 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.155-602C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164953383 | ||||||
| chr2:164953439
|
C | T | 1 | a0001c0001t0028g0198 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.155-658G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164953439 | ||||||
| chr2:164953466
|
G | A | 179 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.155-685C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164953466 | ||||||
| chr2:164953729
|
G | C | 179 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.154+902C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164953729 | ||||||
| chr2:164953849
|
C | G | 179 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.154+782G>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164953849 | ||||||
| chr2:164954050
|
G | A | 1 | a0001c0003t0002g0183 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.154+581C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164954050 | ||||||
| chr2:164954312
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.154+319G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164954312 | ||||||
| chr2:164954334
|
C | T | 1 | a0001c0001t0003g0012 | 2 | NA18978.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.154+297G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164954334 | ||||||
| chr2:164954407
|
T | A | 2 | a0001c0001t0011g0184a0001c0001t0011g0185 | 2 | HG01175.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.154+224A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164954407 | ||||||
| chr2:164954576
|
G | A | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.154+55C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164954576 | ||||||
| chr2:164954833
|
T | A | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.40-88A>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 1/11 | chr2 | 164954833 | ||||||
| chr2:164954846
|
T | C | 1 | a0002c0002t0008g0310 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.40-101A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 1/11 | chr2 | 164954846 | ||||||
| chr2:164954897
|
A | G | 10 | a0001c0001t0007g0187a0001c0001t0007g0188a0001c0001t0007g0189others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-152T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 1/11 | chr2 | 164954897 | ||||||
| chr2:164955038
|
T | C | 1 | a0001c0001t0003g0186 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.39+171A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 1/11 | chr2 | 164955038 | ||||||
| chr2:164955044
|
G | GAA | 6 | a0001c0001t0002g0291a0001c0001t0002g0292a0001c0001t0010g0293others(3): Show | 6 | HG02109.hp1 HG02818.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+163_39+164dupTT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 1/11 | chr2 | 164955044 | ||||||
| chr2:164955044
|
GA | G | 92 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0204others(89): Show | 110 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.39+164delT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 1/11 | chr2 | 164955044 | ||||||
| chr2:164955044
|
GAA | G | 165 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 201 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.39+163_39+164delTT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 1/11 | chr2 | 164955044 | ||||||
| chr2:164955172
|
C | A | 16 | a0002c0002t0008g0297a0002c0002t0008g0299a0002c0002t0008g0302others(13): Show | 17 | HG00423.hp2 HG02040.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.39+37G>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 1/11 | chr2 | 164955172 | ||||||
| chr2:164955196
|
T | C | 1 | a0002c0002t0009g0311 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.39+13A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 1/11 | chr2 | 164955196 |