Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MGYQR others(457): Show |
chr2 | 164889354 | 164960525 |
| a0002 | 0/0 | 462 | 18 | 0 | 0 | 17 | 0 | 1 | 13 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | MGYQR others(457): Show |
chr2 | 164889354 | 164960525 |
| a0003 | 0/0 | 462 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | MGYQR others(457): Show |
chr2 | 164889354 | 164960525 |
| a0004 | 0/0 | 462 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | MGYQR others(457): Show |
chr2 | 164889354 | 164960525 |
| a0005 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | MGYQR others(457): Show |
chr2 | 164889354 | 164960525 |
| a0006 | 0/0 | 462 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | MGYQR others(457): Show |
chr2 | 164889354 | 164960525 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1386 | 338 | 63 | 66 | 163 | 14 | 30 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | ATGGG others(1381): Show |
chr2 | 164889354 | 164960525 | ||
| a0001c0003 | 0/0 | 1386 | 14 | 14 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | ATGGG others(1381): Show |
chr2 | 164889354 | 164960525 | ||
| a0002c0002 | 0/0 | 1386 | 18 | 0 | 0 | 17 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | ATGGG others(1381): Show |
chr2 | 164889354 | 164960525 | ||
| a0003c0004 | 0/0 | 1386 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | ATGGG others(1381): Show |
chr2 | 164889354 | 164960525 | ||
| a0004c0007 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | ATGGG others(1381): Show |
chr2 | 164889354 | 164960525 | ||
| a0005c0006 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | ATGGG others(1381): Show |
chr2 | 164889354 | 164960525 | ||
| a0006c0005 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | ATGGG others(1381): Show |
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 | AGAAA others(5746): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0002 | 0/0 | 5750 | 77 | 14 | 31 | 19 | 8 | 5 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0003 | 0/0 | 5749 | 55 | 1 | 8 | 34 | 3 | 9 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5744): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0004 | 0/0 | 5749 | 22 | 0 | 0 | 22 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5744): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0005 | 1/0 | 5750 | 17 | 15 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0006 | 0/0 | 5750 | 14 | 0 | 0 | 14 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0007 | 0/0 | 5750 | 12 | 10 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0010 | 0/0 | 5751 | 4 | 4 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5746): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0011 | 0/0 | 5750 | 4 | 2 | 2 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0012 | 0/0 | 5750 | 4 | 1 | 2 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0013 | 0/0 | 5749 | 3 | 3 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5744): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0014 | 0/0 | 5750 | 2 | 0 | 1 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0015 | 0/0 | 5750 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0016 | 0/0 | 5750 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0017 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0018 | 0/0 | 5750 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0019 | 0/0 | 5751 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5746): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0020 | 0/0 | 5751 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5746): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0021 | 0/0 | 5751 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5746): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0022 | 0/0 | 5751 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5746): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0023 | 0/0 | 5749 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5744): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0024 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0025 | 0/0 | 5750 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0026 | 0/0 | 5751 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5746): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0027 | 0/0 | 5750 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0028 | 0/0 | 5749 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5744): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0029 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0030 | 0/0 | 5749 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5744): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0032 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0033 | 0/0 | 5750 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0034 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0001t0035 | 0/0 | 5750 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0001c0003t0002 | 0/0 | 5750 | 14 | 14 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0002c0002t0008 | 0/0 | 5751 | 11 | 0 | 0 | 11 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5746): Show |
chr2 | 164889354 | 164960525 |
| a0002c0002t0009 | 0/0 | 5745 | 6 | 0 | 0 | 6 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5740): Show |
chr2 | 164889354 | 164960525 |
| a0002c0002t0031 | 0/0 | 5750 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| a0003c0004t0001 | 0/0 | 5751 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5746): Show |
chr2 | 164889354 | 164960525 |
| a0004c0007t0004 | 0/0 | 5749 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5744): Show |
chr2 | 164889354 | 164960525 |
| a0005c0006t0010 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5746): Show |
chr2 | 164889354 | 164960525 |
| a0006c0005t0002 | 0/0 | 5750 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | AGAAA others(5745): Show |
chr2 | 164889354 | 164960525 |
| actghapid | grch38/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 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0001c0001t0001g0125 | 0/1 | 1 | 0 | 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 |
| a0004c0007t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0005c0006t0010g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| a0006c0005t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | a0004 | 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 | g0124 | 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 | a0005 | 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 | a0006 | 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 | g0123 | 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 | a0001 | c0001 | t0001 | g0125 | REF | REF | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0003 | REF | REF | SLC38A11_chr2_164889354_164960525 | SLC38A11 | chr2 | 164889354 | 164960525 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164908641 | T | C | 1 | a0004 | 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 | a0005 | 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 | a0006 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164898473 | 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164894489 | 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 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0025 others(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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0014 others(8): Show |
127 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(124): 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 | a0001c0001t0022 a0001c0001t0024 |
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 | a0001c0001t0010 a0001c0001t0022 a0001c0001t0024 others(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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0023 others(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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0012 others(10): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): 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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(35): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): 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 | a0001c0001t0011 a0001c0001t0027 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(20): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): 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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0019 others(8): Show |
126 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(123): 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 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0014 others(9): Show |
128 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(125): 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 | a0002c0002t0008 a0002c0002t0009 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164898967 | C | T | 2 | a0001c0001t0016g0258 a0001c0001t0016g0262 |
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 | a0001c0001t0002g0095 a0001c0001t0002g0291 a0001c0001t0002g0292 others(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 | a0001c0001t0012g0036 a0001c0001t0012g0255 a0001c0001t0012g0257 |
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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0002c0002t0008g0297 a0002c0002t0008g0304 a0002c0002t0008g0309 |
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 | 298 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1096-1493A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164900223 | |||||||
| chr2:164900340 | A | G | 225 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(222): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): 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 | a0001c0001t0001g0124 a0001c0001t0001g0157 a0001c0001t0001g0158 |
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 | a0001c0001t0028g0198 a0004c0007t0004g0228 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0130 a0001c0001t0002g0139 others(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 | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
126 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1096-3304dupA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164902033 | |||||||
| chr2:164902033 | CT | C | 6 | a0001c0001t0002g0221 a0001c0001t0002g0278 a0001c0001t0007g0187 others(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 | a0001c0003t0002g0023 a0001c0003t0002g0163 a0001c0003t0002g0164 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0291 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0129 |
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 | a0001c0001t0016g0258 a0001c0001t0016g0262 |
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 | 116 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): 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 | a0001c0001t0010g0293 a0001c0001t0010g0294 a0001c0001t0010g0295 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0291 a0001c0001t0002g0292 others(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 | 298 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): 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 | a0001c0001t0003g0053 a0001c0001t0003g0060 |
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 | a0001c0001t0006g0026 a0001c0001t0006g0028 a0001c0001t0006g0029 others(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 | 206 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): 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 | a0001c0001t0015g0267 a0001c0001t0015g0281 |
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 | a0001c0001t0015g0267 a0001c0001t0015g0281 |
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 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0010 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0118 |
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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | 116 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1095+3375C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 11/11 | chr2 | 164905265 | |||||||
| chr2:164905293 | C | G | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): Show |
120 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(117): 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 | 140 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
159 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(156): 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 | a0001c0001t0002g0048 a0001c0001t0002g0201 |
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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0017g0220 others(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 | a0001c0001t0001g0064 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | 8 | a0001c0001t0001g0042 a0001c0001t0001g0063 a0001c0001t0001g0102 others(5): Show |
8 | HG02056.hp2 HG02074.hp2 HG02155.hp2 others(5): 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 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0056 a0001c0001t0002g0098 a0001c0001t0003g0066 others(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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | a0001c0001t0012g0036 a0001c0001t0012g0255 a0001c0001t0012g0257 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0291 a0001c0001t0002g0292 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 |
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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | a0001c0001t0010g0293 a0001c0001t0010g0294 a0001c0001t0010g0295 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0006g0026 a0001c0001t0006g0028 a0001c0001t0006g0029 others(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 | a0001c0001t0006g0026 a0001c0001t0006g0028 a0001c0001t0006g0029 others(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 | a0001c0001t0001g0154 a0001c0001t0002g0271 |
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 | a0001c0001t0011g0181 a0001c0001t0011g0182 a0001c0001t0011g0184 others(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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 |
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 | 207 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.851-793T>C | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 9/11 | chr2 | 164912541 | |||||||
| chr2:164912674 | C | G | 207 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): 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 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0010g0293 a0001c0001t0010g0294 a0001c0001t0010g0295 others(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 | 208 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): 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 | 118 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): 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 | a0001c0001t0002g0095 a0001c0001t0002g0291 a0001c0001t0002g0292 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0015 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0120 |
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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0007g0187 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0291 a0001c0001t0002g0292 others(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 | 152 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
171 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(168): 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 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | a0001c0001t0003g0229 a0001c0001t0003g0268 a0001c0001t0003g0273 others(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 | a0001c0001t0001g0124 | 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 | a0001c0001t0002g0210 a0001c0001t0006g0026 a0001c0001t0006g0028 others(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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
174 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(171): 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 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(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 | 214 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): 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 | a0001c0001t0006g0026 a0001c0001t0006g0202 a0001c0001t0006g0203 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0076 a0001c0001t0003g0127 |
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 | 211 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): 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 | a0001c0001t0002g0210 a0001c0001t0006g0026 a0001c0001t0006g0028 others(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 | a0005c0006t0010g0254 | 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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | 211 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): 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 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0010 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0133 |
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 | 281 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(278): Show |
335 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(332): 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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0213 |
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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0002g0002 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0160 a0001c0001t0001g0161 others(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 | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
124 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(121): 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 | 281 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(278): Show |
335 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(332): 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 | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
131 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(128): 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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0010g0293 a0001c0001t0010g0294 a0001c0001t0010g0295 others(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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
119 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.618-4306dupT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164920278 | |||||||
| chr2:164920278 | TA | T | 92 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | 187 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): 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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0003g0065 a0001c0001t0003g0071 |
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 | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
128 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(125): 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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0007g0189 a0001c0001t0007g0190 |
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 | a0001c0001t0011g0181 a0001c0001t0011g0182 a0001c0001t0011g0184 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0032 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | 214 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): 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 | a0001c0001t0003g0229 a0001c0001t0003g0273 a0001c0001t0003g0274 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0010g0293 a0001c0001t0010g0294 a0001c0001t0010g0295 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0147 a0001c0001t0029g0284 |
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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0148 a0001c0001t0002g0095 a0001c0001t0002g0096 others(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 | 108 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
124 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(121): 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 | a0001c0001t0013g0251 a0001c0001t0013g0252 a0001c0001t0013g0253 |
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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0032 others(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 | 214 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): 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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | 281 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(278): Show |
335 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(332): 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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0002g0050 a0001c0001t0003g0001 a0001c0001t0003g0004 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0002g0048 a0001c0001t0003g0072 |
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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0010g0293 a0001c0001t0010g0294 a0001c0001t0010g0295 others(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 | a0001c0001t0010g0293 a0001c0001t0010g0294 a0001c0001t0010g0295 others(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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0004g0033 a0001c0001t0023g0241 |
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 | 104 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
119 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(116): 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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0005c0006t0010g0254 | 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 | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): Show |
120 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(117): 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 | a0001c0001t0001g0119 a0001c0001t0001g0131 a0001c0001t0001g0170 |
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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0004g0062 a0001c0001t0004g0073 |
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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0034g0261 |
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 | a0001c0001t0002g0095 a0001c0001t0002g0291 a0001c0001t0002g0292 others(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 | 201 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): 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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0003g0079 a0001c0001t0003g0080 |
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 | 150 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): 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 | a0001c0001t0002g0048 a0001c0001t0002g0050 a0001c0001t0003g0014 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0225 a0001c0001t0001g0246 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0225 a0001c0001t0001g0226 others(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 | 261 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(258): Show |
314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): 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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | a0001c0001t0003g0076 a0001c0001t0003g0127 |
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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0003c0004t0001g0137 a0003c0004t0001g0138 |
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 | 83 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
96 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.617+6487C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164930863 | |||||||
| chr2:164930946 | A | G | 270 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(267): Show |
324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): 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 | a0001c0001t0015g0267 a0001c0001t0032g0280 |
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 | 281 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(278): Show |
335 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(332): 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 | a0001c0001t0012g0036 a0001c0001t0012g0255 a0001c0001t0016g0258 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0257 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0265 a0001c0001t0002g0272 others(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 | a0001c0003t0002g0023 a0001c0003t0002g0163 a0001c0003t0002g0164 others(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 | 195 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.617+6108delT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164931241 | |||||||
| chr2:164931241 | CAA | C | 8 | a0001c0001t0001g0108 a0001c0001t0001g0118 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0133 |
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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0005g0287 a0001c0001t0005g0288 |
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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | 270 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(267): Show |
324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): 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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | a0001c0001t0002g0210 a0001c0001t0006g0026 a0001c0001t0006g0028 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0176 |
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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | 149 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): 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 | a0002c0002t0009g0041 a0002c0002t0009g0298 a0002c0002t0009g0300 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0003g0075 a0001c0001t0003g0082 a0001c0001t0003g0186 |
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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | 148 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(145): Show |
177 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.617+1843dupT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 7/11 | chr2 | 164935506 | |||||||
| chr2:164935506 | CA | C | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): 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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | a0001c0001t0001g0064 a0001c0001t0003g0001 a0001c0001t0003g0004 others(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 | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): 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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | 84 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
97 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(94): 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 | 83 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
96 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(93): 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 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0106 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0246 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | 264 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): 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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | 256 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(253): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): 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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0002g0048 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | 159 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.431-439delA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164939994 | |||||||
| chr2:164939994 | GTT | G | 6 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): 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 | a0001c0001t0011g0181 a0001c0001t0011g0182 a0001c0001t0013g0251 others(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 | a0001c0001t0002g0030 a0001c0001t0002g0039 a0001c0001t0002g0265 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0037 a0001c0001t0002g0264 others(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 | a0001c0001t0002g0098 a0001c0001t0002g0223 a0001c0001t0003g0051 others(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 | 244 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): 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 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0003g0046 others(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 | a0001c0001t0004g0025 a0001c0001t0004g0033 a0001c0001t0004g0199 others(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 | 256 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(253): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): 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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0007g0187 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0176 a0001c0001t0003g0078 |
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 | a0001c0001t0002g0217 a0001c0001t0003g0268 a0001c0001t0011g0181 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0006g0026 others(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 | a0001c0001t0011g0181 a0001c0001t0011g0182 a0001c0001t0011g0184 others(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 | a0001c0001t0011g0181 a0001c0001t0011g0182 a0001c0001t0011g0184 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0003g0079 a0001c0001t0003g0080 |
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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | 167 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(164): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.430+2136dupT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 5/11 | chr2 | 164942432 | |||||||
| chr2:164942432 | C | CAA | 22 | a0001c0001t0001g0131 a0001c0001t0001g0155 a0001c0001t0002g0061 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0002g0048 others(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 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0006g0026 others(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 | 146 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
175 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(172): 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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | 69 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(66): Show |
82 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.364+337dupA | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 4/11 | chr2 | 164945255 | |||||||
| chr2:164945255 | CT | C | 31 | a0001c0001t0001g0205 a0001c0001t0001g0259 a0001c0001t0001g0263 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | 243 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): 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 | a0001c0001t0011g0181 a0001c0001t0011g0182 a0001c0001t0011g0184 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0259 a0001c0001t0001g0263 others(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 | a0001c0001t0003g0084 a0001c0001t0003g0093 a0001c0001t0004g0044 others(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 | 131 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.230-838delT | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164946564 | |||||||
| chr2:164946564 | CAA | C | 7 | a0001c0001t0001g0113 a0001c0001t0002g0008 a0001c0001t0002g0054 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | 184 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): 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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0054 others(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 | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): 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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | a0001c0001t0002g0037 a0001c0001t0002g0264 a0001c0001t0002g0265 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0189 a0001c0001t0007g0191 others(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 | a0001c0001t0002g0095 a0001c0001t0002g0098 a0001c0001t0022g0166 others(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 | a0001c0001t0002g0097 a0001c0001t0024g0175 a0001c0003t0002g0023 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0282 a0001c0001t0003g0004 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | 66 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(63): Show |
78 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(75): 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 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0100 others(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 | a0001c0001t0002g0030 a0001c0001t0002g0217 a0001c0001t0026g0218 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
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 | a0001c0001t0005g0040 a0001c0001t0005g0286 a0001c0001t0005g0287 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0213 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0159 a0001c0001t0001g0160 others(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 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 others(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 | 272 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(269): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): 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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): 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 | a0001c0001t0007g0191 a0001c0001t0007g0192 a0001c0001t0007g0193 others(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 | 272 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(269): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.230-2754T>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948481 | |||||||
| chr2:164948545 | T | C | 162 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.230-2818A>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164948545 | |||||||
| chr2:164948570 | A | G | 272 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(269): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): 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 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
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 | a0001c0001t0007g0189 a0001c0001t0007g0190 |
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 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0006g0026 others(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 | a0001c0001t0001g0263 a0001c0001t0006g0028 a0001c0001t0006g0207 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0006g0206 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0205 a0001c0001t0002g0201 others(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 | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
126 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(123): 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 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | 208 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
246 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(243): 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 | 208 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
246 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(243): 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 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0012g0036 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0204 a0001c0001t0001g0205 |
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 | 272 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(269): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): 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 | a0001c0001t0006g0026 a0001c0001t0006g0202 a0001c0001t0006g0203 |
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 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0263 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0263 others(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 | a0001c0001t0002g0048 a0001c0001t0002g0050 a0001c0001t0003g0014 others(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 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
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 | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): 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 | a0001c0001t0013g0251 a0001c0001t0013g0252 a0001c0001t0013g0253 |
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 | a0001c0001t0002g0291 a0001c0001t0002g0292 |
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 | 197 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
235 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(232): 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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): 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 | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.229+1555G>A | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 3/11 | chr2 | 164951152 | |||||||
| chr2:164951207 | C | T | 197 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
235 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(232): 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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0011g0181 a0001c0001t0011g0182 a0001c0001t0011g0184 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): 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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): 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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0014g0177 |
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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | 208 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
246 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(243): 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 | 162 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): 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 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0263 others(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 | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
126 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(123): 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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0004g0043 others(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 | 162 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): 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 | a0001c0001t0013g0251 a0001c0001t0013g0252 a0001c0001t0013g0253 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): 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 | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.155-685C>T | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164953466 | |||||||
| chr2:164953729 | G | C | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.154+902C>G | SLC38A11 | ENSG00000169507.10 | transcript | ENST00000685975.1 | protein_coding | 2/11 | chr2 | 164953729 | |||||||
| chr2:164953849 | C | G | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): 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 | a0001c0001t0011g0184 a0001c0001t0011g0185 |
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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 | a0001c0001t0007g0187 a0001c0001t0007g0188 a0001c0001t0007g0189 others(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 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0010g0293 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0204 others(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 | 164 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): 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 | a0002c0002t0008g0297 a0002c0002t0008g0299 a0002c0002t0008g0302 others(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 |