Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55089 |
|---|---|
| ensemblid | ENSG00000139209.16 |
| hgncid | 14679 |
| symbol | SLC38A4 |
| name | solute carrier family 38 member 4 |
| refseq_nuc | NM_018018.5 |
| refseq_prot | NP_060488.2 |
| ensembl_nuc | ENST00000266579.9 |
| ensembl_prot | ENSP00000266579.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 46764761 |
| end | 46825997 |
| strand | - |
| ver | v1.2 |
| region | chr12:46764761-46825997 |
| region5000 | chr12:46759761-46830997 |
| regionname0 | SLC38A4_chr12_46764761_46825997 |
| regionname5000 | SLC38A4_chr12_46759761_46830997 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 547 | 266 | 66 | 45 | 120 | 9 | 24 | 101 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0002 | 0/0 | 547 | 54 | 1 | 4 | 43 | 1 | 5 | 31 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0003 | 0/0 | 547 | 42 | 24 | 1 | 16 | 0 | 1 | 13 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0004 | 0/0 | 547 | 11 | 0 | 10 | 1 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0005 | 0/0 | 241 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0006 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0007 | 0/0 | 231 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0008 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0009 | 0/0 | 547 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0010 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0011 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0012 | 0/0 | 547 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0013 | 0/0 | 547 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0014 | 0/0 | 547 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1644 | 260 | 61 | 45 | 119 | 9 | 24 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0002 | 0/0 | 1644 | 54 | 1 | 4 | 43 | 1 | 5 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0003 | 0/0 | 1644 | 42 | 24 | 1 | 16 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0004 | 0/0 | 1644 | 11 | 0 | 10 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0005 | 0/0 | 1644 | 3 | 3 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0006 | 0/0 | 1644 | 2 | 0 | 0 | 0 | 0 | 2 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0007 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0008 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0009 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0010 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0011 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0012 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0013 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0014 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0015 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0016 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0017 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| c0018 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2340 | 188 | 35 | 41 | 83 | 7 | 21 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0002 | 0/0 | 2340 | 104 | 35 | 11 | 57 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0003 | 0/0 | 2340 | 23 | 9 | 2 | 9 | 0 | 3 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0004 | 0/0 | 2340 | 23 | 0 | 2 | 21 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0005 | 0/0 | 2340 | 20 | 0 | 1 | 9 | 3 | 7 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0006 | 0/0 | 2340 | 6 | 6 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0007 | 0/0 | 2340 | 3 | 0 | 2 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0008 | 0/0 | 2340 | 3 | 3 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0009 | 1/0 | 2340 | 2 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0010 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0011 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0012 | 0/0 | 2340 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0013 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0014 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0015 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0016 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0017 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0018 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0019 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| t0020 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1644 | 260 | 61 | 45 | 119 | 9 | 24 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0005 | 0/0 | 1644 | 3 | 3 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0008 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0010 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0016 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0002c0002 | 0/0 | 1644 | 54 | 1 | 4 | 43 | 1 | 5 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0003c0003 | 0/0 | 1644 | 42 | 24 | 1 | 16 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0004c0004 | 0/0 | 1644 | 11 | 0 | 10 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0005c0006 | 0/0 | 1644 | 2 | 0 | 0 | 0 | 0 | 2 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0006c0018 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0007c0009 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0008c0013 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0009c0014 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0010c0015 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0011c0017 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0012c0012 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0013c0011 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0014c0007 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3983 | 167 | 30 | 39 | 77 | 6 | 14 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0002 | 0/0 | 3983 | 9 | 7 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0003 | 0/0 | 3983 | 21 | 8 | 1 | 9 | 0 | 3 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0004 | 0/0 | 3983 | 23 | 0 | 2 | 21 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0005 | 0/0 | 3983 | 19 | 0 | 1 | 9 | 3 | 6 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0006 | 0/0 | 3983 | 6 | 6 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0007 | 0/0 | 3983 | 3 | 0 | 2 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0008 | 0/0 | 3983 | 3 | 3 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0009 | 1/0 | 3983 | 2 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0010 | 0/0 | 3983 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0016 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0017 | 0/0 | 3983 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0018 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0019 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0001t0020 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0005t0001 | 0/0 | 3983 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0005t0015 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0008t0001 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0010t0001 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0001c0016t0001 | 0/0 | 3983 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0002c0002t0001 | 0/0 | 3983 | 11 | 0 | 2 | 5 | 1 | 3 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0002c0002t0002 | 0/0 | 3983 | 38 | 1 | 0 | 37 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0002c0002t0003 | 0/0 | 3983 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0002c0002t0005 | 0/0 | 3983 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0002c0002t0012 | 0/0 | 3983 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0002c0002t0013 | 0/0 | 3983 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0002c0002t0014 | 0/0 | 3983 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0003c0003t0002 | 0/0 | 3983 | 42 | 24 | 1 | 16 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0004c0004t0002 | 0/0 | 3983 | 11 | 0 | 10 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0005c0006t0001 | 0/0 | 3983 | 2 | 0 | 0 | 0 | 0 | 2 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0006c0018t0002 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0007c0009t0002 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0008c0013t0001 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0009c0014t0001 | 0/0 | 3983 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0010c0015t0003 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0011c0017t0002 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0012c0012t0001 | 0/0 | 3983 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0013c0011t0002 | 0/0 | 3983 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| a0014c0007t0011 | 0/0 | 3983 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | copy fasta | chr12 | 46759761 | 46830997 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0006g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0006g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0006g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0006g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0006g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0006g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0007g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0007g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0009g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0010g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0016g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0017g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0018g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0019g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0020g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0005t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0005t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0005t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0008t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0010t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0016t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0012g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0013g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0014g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0004c0004t0002g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0004c0004t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0004c0004t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0004c0004t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0004c0004t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0004c0004t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0004c0004t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0005c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0005c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0006c0018t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0007c0009t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0008c0013t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0009c0014t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0010c0015t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0011c0017t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0012c0012t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0013c0011t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0014c0007t0011g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0076 | EUR | FIN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | FIN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00642 | hp1 | a0002 | c0002 | t0013 | g0104 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00673 | hp1 | a0003 | c0003 | t0002 | g0285 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01071 | hp2 | a0004 | c0004 | t0002 | g0002 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01109 | hp1 | a0004 | c0004 | t0002 | g0061 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01175 | hp1 | a0002 | c0002 | t0003 | g0063 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01192 | hp2 | a0003 | c0003 | t0002 | g0247 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0022 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0022 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01496 | hp2 | a0004 | c0004 | t0002 | g0002 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0027 | EUR | IBS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0037 | EUR | IBS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0027 | EUR | IBS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01884 | hp1 | a0001 | c0010 | t0001 | g0326 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01884 | hp2 | a0003 | c0003 | t0002 | g0289 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01928 | hp2 | a0004 | c0004 | t0002 | g0065 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01975 | hp1 | a0004 | c0004 | t0002 | g0002 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01981 | hp1 | a0004 | c0004 | t0002 | g0064 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01993 | hp2 | a0004 | c0004 | t0002 | g0007 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02055 | hp1 | a0003 | c0003 | t0002 | g0287 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0335 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02080 | hp1 | a0003 | c0003 | t0002 | g0283 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0238 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0339 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02145 | hp2 | a0011 | c0017 | t0002 | g0168 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02148 | hp1 | a0004 | c0004 | t0002 | g0007 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02155 | hp2 | a0003 | c0003 | t0002 | g0136 | EAS | CDX | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02257 | hp1 | a0001 | c0001 | t0016 | g0172 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02258 | hp1 | a0001 | c0005 | t0015 | g0052 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02258 | hp2 | a0010 | c0015 | t0003 | g0293 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02273 | hp2 | a0004 | c0004 | t0002 | g0002 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02280 | hp1 | a0003 | c0003 | t0002 | g0253 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02300 | hp1 | a0004 | c0004 | t0002 | g0066 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02451 | hp2 | a0003 | c0003 | t0002 | g0270 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0331 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02572 | hp2 | a0003 | c0003 | t0002 | g0251 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0057 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02602 | hp2 | a0009 | c0014 | t0001 | g0224 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02615 | hp1 | a0003 | c0003 | t0002 | g0281 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0337 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0305 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02683 | hp1 | a0001 | c0001 | t0007 | g0214 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02683 | hp2 | a0012 | c0012 | t0001 | g0106 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0044 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02717 | hp1 | a0003 | c0003 | t0002 | g0252 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0336 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0100 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02818 | hp1 | a0001 | c0008 | t0001 | g0099 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02818 | hp2 | a0006 | c0018 | t0002 | g0288 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02886 | hp1 | a0003 | c0003 | t0002 | g0108 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0291 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02896 | hp2 | a0003 | c0003 | t0002 | g0026 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02897 | hp2 | a0003 | c0003 | t0002 | g0026 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0306 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02965 | hp2 | a0003 | c0003 | t0002 | g0272 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02970 | hp1 | a0001 | c0001 | t0020 | g0340 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02970 | hp2 | a0003 | c0003 | t0002 | g0254 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0297 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0280 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03098 | hp1 | a0003 | c0003 | t0002 | g0249 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0338 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0279 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03139 | hp1 | a0003 | c0003 | t0002 | g0170 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03139 | hp2 | a0001 | c0001 | t0018 | g0098 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03195 | hp2 | a0007 | c0009 | t0002 | g0248 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03209 | hp2 | a0003 | c0003 | t0002 | g0274 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0292 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0171 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03453 | hp1 | a0003 | c0003 | t0002 | g0276 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03486 | hp2 | a0003 | c0003 | t0002 | g0278 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03491 | hp2 | a0005 | c0006 | t0001 | g0078 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03492 | hp2 | a0005 | c0006 | t0001 | g0077 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03516 | hp2 | a0003 | c0003 | t0002 | g0208 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03540 | hp1 | a0003 | c0003 | t0002 | g0127 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0058 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0167 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03579 | hp2 | a0003 | c0003 | t0002 | g0273 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03688 | hp2 | a0003 | c0003 | t0002 | g0286 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0036 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0189 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0237 | SAS | BEB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0140 | SAS | BEB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04184 | hp1 | a0002 | c0002 | t0012 | g0074 | SAS | BEB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | BEB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0217 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04228 | hp2 | a0002 | c0002 | t0005 | g0071 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | CHB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | CHB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0169 | AFR | YRI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18906 | hp2 | a0003 | c0003 | t0002 | g0317 | AFR | YRI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18945 | hp1 | a0003 | c0003 | t0002 | g0267 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18947 | hp1 | a0004 | c0004 | t0002 | g0201 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18953 | hp1 | a0003 | c0003 | t0002 | g0222 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18962 | hp2 | a0013 | c0011 | t0002 | g0264 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18967 | hp1 | a0001 | c0001 | t0017 | g0196 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18969 | hp2 | a0003 | c0003 | t0002 | g0260 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18974 | hp1 | a0003 | c0003 | t0002 | g0263 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18978 | hp2 | a0003 | c0003 | t0002 | g0284 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18984 | hp2 | a0002 | c0002 | t0014 | g0315 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18989 | hp1 | a0003 | c0003 | t0002 | g0207 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18989 | hp2 | a0003 | c0003 | t0002 | g0268 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18998 | hp1 | a0014 | c0007 | t0011 | g0070 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18999 | hp2 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19000 | hp2 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0312 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19009 | hp2 | a0003 | c0003 | t0002 | g0028 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | LWK | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | LWK | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0282 | AFR | LWK | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0223 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19060 | hp2 | a0003 | c0003 | t0002 | g0028 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19062 | hp1 | a0003 | c0003 | t0002 | g0266 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0084 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19075 | hp1 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0259 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19091 | hp1 | a0001 | c0016 | t0001 | g0147 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19240 | hp1 | a0003 | c0003 | t0002 | g0107 | AFR | YRI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19240 | hp2 | a0001 | c0001 | t0019 | g0334 | AFR | YRI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ASW | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20129 | hp2 | a0003 | c0003 | t0002 | g0250 | AFR | ASW | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | TSI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | GIH | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0040 | SAS | GIH | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02109 | hp1 | a0003 | c0003 | t0002 | g0277 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0333 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | USA | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20300 | hp1 | a0008 | c0013 | t0001 | g0193 | AFR | USA | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | USA | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0221 | REF | REF | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0009 | g0101 | REF | REF | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:46768312
|
C | T | 1 | a0011 | 1 | HG02145.hp2 | missense_variant&splice_region_variant | MODERATE | c.1540G>A | p.Gly514Arg | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/17 | 1939/3983 | 1540/1644 | 514/547 | chr12 | 46768312 | ||
| chr12:46775117
|
G | C | 1 | a0010 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1231C>G | p.Pro411Ala | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/17 | 1630/3983 | 1231/1644 | 411/547 | chr12 | 46775117 | ||
| chr12:46776949
|
C | T | 1 | a0009 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.1129G>A | p.Val377Ile | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/17 | 1528/3983 | 1129/1644 | 377/547 | chr12 | 46776949 | ||
| chr12:46776981
|
G | A | 5 | a0003a0004a0006others(2): Show | 56 | HG00673.hp1 HG01071.hp2 HG01109.hp1 others(53): Show |
missense_variant | MODERATE | c.1097C>T | p.Thr366Met | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/17 | 1496/3983 | 1097/1644 | 366/547 | chr12 | 46776981 | ||
| chr12:46776996
|
C | T | 1 | a0008 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1082G>A | p.Arg361Gln | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/17 | 1481/3983 | 1082/1644 | 361/547 | chr12 | 46776996 | ||
| chr12:46778602
|
C | T | 1 | a0014 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.892G>A | p.Asp298Asn | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 11/17 | 1291/3983 | 892/1644 | 298/547 | chr12 | 46778602 | ||
| chr12:46778634
|
A | G | 1 | a0012 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.860T>C | p.Met287Thr | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 11/17 | 1259/3983 | 860/1644 | 287/547 | chr12 | 46778634 | ||
| chr12:46778639
|
G | T | 1 | a0013 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.855C>A | p.Phe285Leu | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 11/17 | 1254/3983 | 855/1644 | 285/547 | chr12 | 46778639 | ||
| chr12:46778768
|
G | T | 1 | a0005 | 2 | HG03491.hp2 HG03492.hp2 |
stop_gained | HIGH | c.726C>A | p.Tyr242* | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 11/17 | 1125/3983 | 726/1644 | 242/547 | chr12 | 46778768 | ||
| chr12:46779632
|
G | T | 1 | a0007 | 1 | HG03195.hp2 | stop_gained | HIGH | c.696C>A | p.Cys232* | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 10/17 | 1095/3983 | 696/1644 | 232/547 | chr12 | 46779632 | ||
| chr12:46792987
|
C | T | 4 | a0002a0004a0005others(1): Show | 68 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
missense_variant | MODERATE | c.85G>A | p.Gly29Arg | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/17 | 484/3983 | 85/1644 | 29/547 | chr12 | 46792987 | ||
| chr12:46793008
|
T | C | 1 | a0006 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.64A>G | p.Ser22Gly | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/17 | 463/3983 | 64/1644 | 22/547 | chr12 | 46793008 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:46778648
|
A | G | 1 | a0001c0010 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.846T>C | p.Asp282Asp | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 11/17 | 1245/3983 | 846/1644 | 282/547 | chr12 | 46778648 | ||
| chr12:46779796
|
C | T | 1 | a0001c0008 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.642G>A | p.Ser214Ser | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 9/17 | 1041/3983 | 642/1644 | 214/547 | chr12 | 46779796 | ||
| chr12:46787951
|
G | A | 1 | a0001c0016 | 1 | NA19091.hp1 | synonymous_variant | LOW | c.291C>T | p.Ser97Ser | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/17 | 690/3983 | 291/1644 | 97/547 | chr12 | 46787951 | ||
| chr12:46788026
|
G | A | 2 | a0001c0005a0011c0017 | 4 | HG02145.hp2 HG02258.hp1 HG02622.hp2 others(1): Show |
synonymous_variant | LOW | c.216C>T | p.Pro72Pro | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/17 | 615/3983 | 216/1644 | 72/547 | chr12 | 46788026 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:46764809
|
T | C | 1 | a0002c0002t0013 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1892A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1892 | chr12 | 46764809 | |||||
| chr12:46764976
|
G | A | 1 | a0001c0005t0015 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1725C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1725 | chr12 | 46764976 | |||||
| chr12:46765100
|
G | C | 1 | a0001c0001t0004 | 23 | HG01257.hp1 HG01258.hp1 HG02074.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1601C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1601 | chr12 | 46765100 | |||||
| chr12:46765165
|
A | T | 2 | a0002c0002t0012a0002c0002t0013 | 2 | HG00642.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1536T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1536 | chr12 | 46765165 | |||||
| chr12:46765185
|
A | G | 7 | a0001c0001t0003a0001c0001t0005a0001c0001t0020others(4): Show | 45 | HG00423.hp1 HG01099.hp2 HG01175.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1516T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1516 | chr12 | 46765185 | |||||
| chr12:46765190
|
T | A | 1 | a0001c0001t0007 | 3 | HG01433.hp2 HG01496.hp1 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1511A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1511 | chr12 | 46765190 | |||||
| chr12:46765212
|
G | A | 2 | a0001c0001t0005a0002c0002t0005 | 20 | HG01099.hp2 HG01515.hp1 HG01516.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1489C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1489 | chr12 | 46765212 | |||||
| chr12:46765301
|
G | A | 1 | a0002c0002t0014 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1400C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1400 | chr12 | 46765301 | |||||
| chr12:46765340
|
A | G | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | 382 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(379): Show |
3_prime_UTR_variant | MODIFIER | c.*1361T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1361 | chr12 | 46765340 | |||||
| chr12:46765368
|
G | A | 2 | a0001c0001t0004a0001c0001t0010 | 25 | HG01257.hp1 HG01258.hp1 HG02074.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1333C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1333 | chr12 | 46765368 | |||||
| chr12:46765405
|
T | A | 1 | a0001c0001t0016 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1296A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1296 | chr12 | 46765405 | |||||
| chr12:46765413
|
A | T | 18 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(15): Show | 205 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*1288T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1288 | chr12 | 46765413 | |||||
| chr12:46765637
|
C | A | 1 | a0001c0001t0017 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1064G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 1064 | chr12 | 46765637 | |||||
| chr12:46766442
|
C | T | 1 | a0014c0007t0011 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*259G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 259 | chr12 | 46766442 | |||||
| chr12:46766476
|
G | A | 1 | a0001c0001t0008 | 3 | HG03041.hp1 HG03130.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*225C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 225 | chr12 | 46766476 | |||||
| chr12:46766501
|
T | C | 1 | a0001c0001t0018 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*200A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 17/17 | 200 | chr12 | 46766501 | |||||
| chr12:46825915
|
G | A | 2 | a0001c0001t0006a0001c0001t0019 | 7 | HG02055.hp2 HG02145.hp1 HG02615.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-317C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/17 | 32844 | chr12 | 46825915 | |||||
| chr12:46825955
|
G | A | 1 | a0001c0001t0020 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-357C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/17 | 32884 | chr12 | 46825955 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:46767238
|
A | ATG | 9 | a0001c0001t0002g0035a0001c0001t0002g0162a0001c0001t0002g0301others(6): Show | 9 | HG01192.hp2 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1543-438_1543-437d others(4): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46767238 | ||||||
| chr12:46767238
|
ATG | A | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(178): Show | 203 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1543-438_1543-437d others(4): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46767238 | ||||||
| chr12:46767495
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1543-693G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46767495 | ||||||
| chr12:46767529
|
C | T | 19 | a0001c0001t0005g0027a0001c0001t0005g0036a0001c0001t0005g0037others(16): Show | 20 | HG01099.hp2 HG01515.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.1543-727G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46767529 | ||||||
| chr12:46767592
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1542+718G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46767592 | ||||||
| chr12:46767764
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1542+546A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46767764 | ||||||
| chr12:46767830
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0001g0269 | 2 | HG00408.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1542+480G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46767830 | ||||||
| chr12:46767934
|
A | G | 1 | a0002c0002t0013g0104 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1542+376T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46767934 | ||||||
| chr12:46767957
|
A | G | 1 | a0001c0001t0005g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1542+353T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46767957 | ||||||
| chr12:46767969
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0244 | 2 | HG02735.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1542+341G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46767969 | ||||||
| chr12:46768029
|
T | G | 1 | a0001c0001t0005g0187 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1542+281A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46768029 | ||||||
| chr12:46768192
|
G | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(180): Show | 205 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1542+118C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46768192 | ||||||
| chr12:46768428
|
C | T | 63 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(60): Show | 71 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1445-21G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 15/16 | chr12 | 46768428 | ||||||
| chr12:46768525
|
A | G | 1 | a0001c0001t0005g0187 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1445-118T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 15/16 | chr12 | 46768525 | ||||||
| chr12:46768635
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1445-228T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 15/16 | chr12 | 46768635 | ||||||
| chr12:46768866
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0239 | 2 | NA18947.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1444+418T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 15/16 | chr12 | 46768866 | ||||||
| chr12:46768926
|
G | A | 1 | a0002c0002t0001g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1444+358C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 15/16 | chr12 | 46768926 | ||||||
| chr12:46769106
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(180): Show | 205 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1444+178T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 15/16 | chr12 | 46769106 | ||||||
| chr12:46769155
|
T | G | 338 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(335): Show | 382 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(379): Show |
intron_variant | MODIFIER | c.1444+129A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 15/16 | chr12 | 46769155 | ||||||
| chr12:46769174
|
A | G | 48 | a0001c0001t0002g0290a0001c0001t0002g0302a0001c0001t0002g0306others(45): Show | 55 | HG00673.hp1 HG01071.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1444+110T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 15/16 | chr12 | 46769174 | ||||||
| chr12:46769470
|
T | C | 3 | a0001c0001t0008g0279a0001c0001t0008g0280a0001c0001t0008g0282 | 3 | HG03041.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1300-42A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46769470 | ||||||
| chr12:46769523
|
C | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(180): Show | 205 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1300-95G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46769523 | ||||||
| chr12:46769731
|
C | T | 24 | a0001c0001t0003g0016a0001c0001t0003g0093a0001c0001t0003g0143others(21): Show | 25 | HG00423.hp1 HG01175.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.1300-303G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46769731 | ||||||
| chr12:46770034
|
C | G | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(271): Show | 305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.1300-606G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46770034 | ||||||
| chr12:46770286
|
CATTTTAA others(19): Show |
C | 2 | a0001c0001t0007g0022a0001c0001t0007g0214 | 3 | HG01433.hp2 HG01496.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1300-884_1300-859d others(28): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46770286 | ||||||
| chr12:46770311
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0092a0001c0001t0001g0304 | 4 | HG01109.hp2 HG02630.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-883C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46770311 | ||||||
| chr12:46770335
|
G | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(180): Show | 205 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1300-907C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46770335 | ||||||
| chr12:46770350
|
T | A | 1 | a0001c0001t0001g0221 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1300-922A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46770350 | ||||||
| chr12:46770529
|
T | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0109others(2): Show | 7 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1300-1101A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46770529 | ||||||
| chr12:46771200
|
A | T | 3 | a0001c0001t0002g0271a0001c0001t0002g0295a0001c0001t0019g0334 | 3 | HG02451.hp1 HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1300-1772T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46771200 | ||||||
| chr12:46771259
|
G | A | 338 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(335): Show | 382 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(379): Show |
intron_variant | MODIFIER | c.1300-1831C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46771259 | ||||||
| chr12:46771280
|
T | C | 2 | a0001c0001t0002g0295a0001c0001t0019g0334 | 2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1300-1852A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46771280 | ||||||
| chr12:46771385
|
A | G | 191 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(188): Show | 213 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1300-1957T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46771385 | ||||||
| chr12:46771540
|
C | G | 191 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(188): Show | 213 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1300-2112G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46771540 | ||||||
| chr12:46771646
|
T | C | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(113): Show | 130 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1300-2218A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46771646 | ||||||
| chr12:46771711
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1300-2283C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46771711 | ||||||
| chr12:46771818
|
G | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0275 | 3 | HG02257.hp2 HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1300-2390C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46771818 | ||||||
| chr12:46772002
|
A | T | 5 | a0001c0001t0002g0290a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-2574T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46772002 | ||||||
| chr12:46772133
|
TA | T | 76 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0031others(73): Show | 90 | HG00673.hp1 HG01071.hp2 HG01109.hp1 others(87): Show |
intron_variant | MODIFIER | c.1300-2706delT | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46772133 | ||||||
| chr12:46772169
|
G | C | 56 | a0001c0001t0001g0089a0001c0001t0002g0258a0001c0001t0004g0006others(53): Show | 69 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1300-2741C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46772169 | ||||||
| chr12:46772313
|
G | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(110): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1299+2736C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46772313 | ||||||
| chr12:46772314
|
C | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(110): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1299+2735G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46772314 | ||||||
| chr12:46772553
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1299+2496G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46772553 | ||||||
| chr12:46772575
|
A | G | 49 | a0003c0003t0002g0018a0003c0003t0002g0026a0003c0003t0002g0028others(46): Show | 56 | HG00673.hp1 HG01071.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1299+2474T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46772575 | ||||||
| chr12:46772809
|
C | A | 1 | a0001c0001t0005g0040 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1299+2240G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46772809 | ||||||
| chr12:46772830
|
T | C | 50 | a0001c0001t0001g0030a0001c0001t0001g0110a0001c0001t0001g0294others(47): Show | 53 | HG00423.hp1 HG01070.hp1 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1299+2219A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46772830 | ||||||
| chr12:46773111
|
T | A | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(175): Show | 199 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1299+1938A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46773111 | ||||||
| chr12:46773178
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1299+1871A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46773178 | ||||||
| chr12:46773253
|
A | G | 338 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(335): Show | 382 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(379): Show |
intron_variant | MODIFIER | c.1299+1796T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46773253 | ||||||
| chr12:46773291
|
C | T | 56 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0020others(53): Show | 63 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.1299+1758G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46773291 | ||||||
| chr12:46773295
|
G | A | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(167): Show | 190 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1299+1754C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46773295 | ||||||
| chr12:46773505
|
C | T | 5 | a0003c0003t0002g0028a0003c0003t0002g0260a0003c0003t0002g0263others(2): Show | 6 | NA18962.hp2 NA18969.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1299+1544G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46773505 | ||||||
| chr12:46773576
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1299+1473A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46773576 | ||||||
| chr12:46774016
|
C | T | 3 | a0001c0001t0002g0271a0001c0001t0002g0295a0001c0001t0019g0334 | 3 | HG02451.hp1 HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1299+1033G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46774016 | ||||||
| chr12:46774054
|
T | C | 31 | a0001c0001t0001g0030a0001c0001t0001g0110a0001c0001t0001g0294others(28): Show | 33 | HG00423.hp1 HG01070.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.1299+995A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46774054 | ||||||
| chr12:46774128
|
C | T | 31 | a0001c0001t0002g0258a0002c0002t0001g0055a0002c0002t0002g0001others(28): Show | 40 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1299+921G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46774128 | ||||||
| chr12:46774218
|
T | C | 5 | a0001c0001t0002g0290a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+831A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46774218 | ||||||
| chr12:46774238
|
A | C | 338 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(335): Show | 382 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(379): Show |
intron_variant | MODIFIER | c.1299+811T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46774238 | ||||||
| chr12:46774249
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1299+800C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46774249 | ||||||
| chr12:46774450
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0275 | 3 | HG02257.hp2 HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1299+599G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46774450 | ||||||
| chr12:46774470
|
G | A | 7 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 7 | HG01167.hp1 HG01257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1299+579C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46774470 | ||||||
| chr12:46774620
|
G | A | 2 | a0003c0003t0002g0276a0006c0018t0002g0288 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1299+429C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46774620 | ||||||
| chr12:46774871
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0092a0001c0001t0001g0304 | 4 | HG01109.hp2 HG02630.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1299+178A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46774871 | ||||||
| chr12:46774877
|
A | G | 15 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0131others(12): Show | 18 | NA18940.hp2 NA18945.hp2 NA18946.hp2 others(15): Show |
intron_variant | MODIFIER | c.1299+172T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46774877 | ||||||
| chr12:46775295
|
C | T | 3 | a0001c0001t0002g0271a0001c0001t0002g0295a0001c0001t0019g0334 | 3 | HG02451.hp1 HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1175-122G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46775295 | ||||||
| chr12:46775479
|
G | A | 32 | a0001c0001t0002g0258a0002c0002t0001g0055a0002c0002t0002g0001others(29): Show | 41 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1175-306C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46775479 | ||||||
| chr12:46775495
|
G | A | 31 | a0001c0001t0001g0030a0001c0001t0001g0110a0001c0001t0001g0294others(28): Show | 33 | HG00423.hp1 HG01070.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.1175-322C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46775495 | ||||||
| chr12:46775559
|
C | T | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(172): Show | 196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1175-386G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46775559 | ||||||
| chr12:46775567
|
C | T | 10 | a0001c0001t0001g0030a0001c0001t0001g0294a0001c0001t0003g0291others(7): Show | 11 | HG02258.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1175-394G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46775567 | ||||||
| chr12:46775579
|
G | T | 2 | a0002c0002t0012g0074a0002c0002t0013g0104 | 2 | HG00642.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1175-406C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46775579 | ||||||
| chr12:46775658
|
A | T | 5 | a0001c0001t0002g0290a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-485T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46775658 | ||||||
| chr12:46775735
|
A | G | 194 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(191): Show | 219 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.1175-562T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46775735 | ||||||
| chr12:46775874
|
T | C | 1 | a0001c0010t0001g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1175-701A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46775874 | ||||||
| chr12:46775899
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1175-726C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46775899 | ||||||
| chr12:46775908
|
G | T | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(172): Show | 196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1175-735C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46775908 | ||||||
| chr12:46775990
|
A | G | 1 | a0002c0002t0013g0104 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1175-817T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46775990 | ||||||
| chr12:46776051
|
A | G | 1 | a0003c0003t0002g0276 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1174+853T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46776051 | ||||||
| chr12:46776074
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0092a0001c0001t0001g0304 | 4 | HG01109.hp2 HG02630.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+830T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46776074 | ||||||
| chr12:46776224
|
T | A | 1 | a0001c0001t0004g0313 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1174+680A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46776224 | ||||||
| chr12:46776407
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0092a0001c0001t0001g0304 | 4 | HG01109.hp2 HG02630.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+497T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46776407 | ||||||
| chr12:46776502
|
G | C | 3 | a0001c0001t0002g0271a0001c0001t0002g0295a0001c0001t0019g0334 | 3 | HG02451.hp1 HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1174+402C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46776502 | ||||||
| chr12:46776538
|
G | T | 338 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(335): Show | 382 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(379): Show |
intron_variant | MODIFIER | c.1174+366C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46776538 | ||||||
| chr12:46776703
|
A | G | 1 | a0001c0005t0001g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1174+201T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46776703 | ||||||
| chr12:46776838
|
C | A | 50 | a0001c0001t0001g0030a0001c0001t0001g0110a0001c0001t0001g0294others(47): Show | 53 | HG00423.hp1 HG01070.hp1 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1174+66G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46776838 | ||||||
| chr12:46776879
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1174+25C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 13/16 | chr12 | 46776879 | ||||||
| chr12:46777025
|
A | C | 1 | a0001c0005t0001g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1074-21T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777025 | ||||||
| chr12:46777104
|
C | A | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(172): Show | 196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1074-100G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777104 | ||||||
| chr12:46777127
|
A | G | 48 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0020others(45): Show | 55 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1074-123T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777127 | ||||||
| chr12:46777213
|
A | G | 1 | a0002c0002t0002g0038 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1074-209T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777213 | ||||||
| chr12:46777273
|
A | G | 1 | a0003c0003t0002g0026 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1074-269T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777273 | ||||||
| chr12:46777303
|
C | G | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(172): Show | 196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1074-299G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777303 | ||||||
| chr12:46777356
|
G | A | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(172): Show | 196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1074-352C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777356 | ||||||
| chr12:46777376
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-372T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777376 | ||||||
| chr12:46777449
|
TG | T | 4 | a0002c0002t0002g0001a0002c0002t0002g0048a0002c0002t0002g0049others(1): Show | 8 | NA18939.hp1 NA18967.hp2 NA18981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1074-446delC | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777449 | ||||||
| chr12:46777657
|
C | T | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(110): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1073+632G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777657 | ||||||
| chr12:46777759
|
T | C | 1 | a0011c0017t0002g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1073+530A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777759 | ||||||
| chr12:46777827
|
G | T | 1 | a0002c0002t0002g0038 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1073+462C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777827 | ||||||
| chr12:46777975
|
G | A | 277 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(274): Show | 308 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.1073+314C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777975 | ||||||
| chr12:46777992
|
T | C | 1 | a0001c0001t0002g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1073+297A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777992 | ||||||
| chr12:46778434
|
A | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0213 | 3 | NA18973.hp2 NA18984.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.994-66T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 11/16 | chr12 | 46778434 | ||||||
| chr12:46778486
|
G | A | 50 | a0001c0001t0009g0100a0003c0003t0002g0018a0003c0003t0002g0026others(47): Show | 57 | HG00673.hp1 HG01071.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.993+15C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 11/16 | chr12 | 46778486 | ||||||
| chr12:46778798
|
G | GA | 7 | a0001c0001t0001g0215a0001c0001t0001g0244a0003c0003t0002g0018others(4): Show | 8 | HG02735.hp1 HG04204.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-23dupT | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 10/16 | chr12 | 46778798 | ||||||
| chr12:46779236
|
G | A | 1 | a0003c0003t0002g0270 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.717+375C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 10/16 | chr12 | 46779236 | ||||||
| chr12:46779280
|
G | A | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(271): Show | 305 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.717+331C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 10/16 | chr12 | 46779280 | ||||||
| chr12:46779375
|
A | T | 1 | a0009c0014t0001g0224 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.717+236T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 10/16 | chr12 | 46779375 | ||||||
| chr12:46779385
|
A | G | 6 | a0001c0001t0001g0088a0001c0001t0006g0335a0001c0001t0006g0336others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+226T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 10/16 | chr12 | 46779385 | ||||||
| chr12:46779608
|
T | C | 3 | a0001c0001t0008g0279a0001c0001t0008g0280a0001c0001t0008g0282 | 3 | HG03041.hp1 HG03130.hp2 NA19043.hp1 |
splice_region_variant&intron_variant | LOW | c.717+3A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 10/16 | chr12 | 46779608 | ||||||
| chr12:46779879
|
A | G | 189 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(186): Show | 213 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.576-17T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 8/16 | chr12 | 46779879 | ||||||
| chr12:46780047
|
G | A | 50 | a0001c0001t0001g0030a0001c0001t0001g0110a0001c0001t0001g0294others(47): Show | 53 | HG00423.hp1 HG01070.hp1 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.494-17C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46780047 | ||||||
| chr12:46780098
|
C | T | 1 | a0004c0004t0002g0066 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.494-68G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46780098 | ||||||
| chr12:46780154
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0092a0001c0001t0001g0304 | 4 | HG01109.hp2 HG02630.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-124A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46780154 | ||||||
| chr12:46780237
|
T | A | 17 | a0001c0001t0001g0110a0001c0001t0003g0016a0001c0001t0003g0093others(14): Show | 18 | HG00423.hp1 HG01070.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.494-207A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46780237 | ||||||
| chr12:46780238
|
C | G | 32 | a0001c0001t0002g0258a0002c0002t0001g0055a0002c0002t0002g0001others(29): Show | 41 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.494-208G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46780238 | ||||||
| chr12:46780306
|
T | C | 59 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0020others(56): Show | 66 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.494-276A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46780306 | ||||||
| chr12:46780371
|
G | T | 1 | a0001c0001t0001g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494-341C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46780371 | ||||||
| chr12:46780533
|
G | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(110): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.494-503C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46780533 | ||||||
| chr12:46780603
|
GT | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(119): Show | 137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.494-574delA | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46780603 | ||||||
| chr12:46780614
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494-584A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46780614 | ||||||
| chr12:46780659
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.494-629A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46780659 | ||||||
| chr12:46780989
|
A | C | 2 | a0002c0002t0002g0067a0014c0007t0011g0070 | 2 | HG00597.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.494-959T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46780989 | ||||||
| chr12:46781051
|
G | A | 1 | a0001c0005t0015g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.494-1021C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46781051 | ||||||
| chr12:46781070
|
T | C | 5 | a0003c0003t0002g0247a0003c0003t0002g0270a0003c0003t0002g0272others(2): Show | 5 | HG01192.hp2 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-1040A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46781070 | ||||||
| chr12:46781209
|
A | G | 2 | a0001c0001t0005g0083a0001c0001t0005g0084 | 2 | NA18959.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.494-1179T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46781209 | ||||||
| chr12:46781256
|
G | T | 1 | a0001c0001t0006g0339 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.494-1226C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46781256 | ||||||
| chr12:46781307
|
C | G | 1 | a0001c0001t0001g0024 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.494-1277G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46781307 | ||||||
| chr12:46781499
|
T | C | 32 | a0001c0001t0001g0014a0001c0001t0001g0105a0001c0001t0001g0114others(29): Show | 37 | HG00408.hp2 HG01257.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.494-1469A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46781499 | ||||||
| chr12:46781686
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.494-1656G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46781686 | ||||||
| chr12:46781703
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0092 | 3 | HG01109.hp2 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.494-1673G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46781703 | ||||||
| chr12:46782039
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494-2009A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782039 | ||||||
| chr12:46782078
|
T | C | 3 | a0001c0001t0004g0323a0001c0001t0004g0325a0001c0001t0004g0332 | 3 | NA18939.hp2 NA19004.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.494-2048A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782078 | ||||||
| chr12:46782083
|
A | T | 48 | a0003c0003t0002g0018a0003c0003t0002g0026a0003c0003t0002g0028others(45): Show | 55 | HG00673.hp1 HG01071.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.494-2053T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782083 | ||||||
| chr12:46782086
|
T | G | 6 | a0001c0001t0001g0031a0001c0001t0002g0290a0001c0001t0002g0301others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-2056A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782086 | ||||||
| chr12:46782159
|
A | G | 1 | a0004c0004t0002g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.494-2129T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782159 | ||||||
| chr12:46782306
|
A | G | 1 | a0001c0001t0002g0271 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.493+2236T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782306 | ||||||
| chr12:46782372
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0092 | 3 | HG01109.hp2 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.493+2170G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782372 | ||||||
| chr12:46782401
|
C | A | 1 | a0002c0002t0002g0050 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.493+2141G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782401 | ||||||
| chr12:46782664
|
G | A | 58 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0020others(55): Show | 64 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.493+1878C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782664 | ||||||
| chr12:46782753
|
C | T | 48 | a0003c0003t0002g0018a0003c0003t0002g0026a0003c0003t0002g0028others(45): Show | 55 | HG00673.hp1 HG01071.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.493+1789G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782753 | ||||||
| chr12:46782794
|
T | C | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(111): Show | 127 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.493+1748A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782794 | ||||||
| chr12:46782945
|
C | T | 1 | a0001c0001t0001g0221 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.493+1597G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782945 | ||||||
| chr12:46782953
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0002g0301 | 3 | HG01167.hp2 HG01169.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.493+1589C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46782953 | ||||||
| chr12:46783020
|
A | ATG | 23 | a0001c0001t0001g0092a0001c0001t0001g0110a0001c0001t0001g0185others(20): Show | 28 | HG00423.hp1 HG01070.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.493+1520_493+1521d others(4): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783020 | ||||||
| chr12:46783020
|
A | ATGTG | 47 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0329others(44): Show | 53 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.493+1518_493+1521d others(6): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783020 | ||||||
| chr12:46783020
|
A | ATGTGTG | 46 | a0001c0001t0001g0031a0001c0001t0001g0177a0001c0001t0001g0178others(43): Show | 56 | HG00642.hp1 HG01071.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.493+1516_493+1521d others(8): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783020 | ||||||
| chr12:46783020
|
A | ATGTGTGT others(1): Show |
35 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0111others(32): Show | 35 | HG01099.hp1 HG01099.hp2 HG01516.hp1 others(32): Show |
intron_variant | MODIFIER | c.493+1514_493+1521d others(10): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783020 | ||||||
| chr12:46783020
|
A | ATGTGTGT others(3): Show |
36 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0020others(33): Show | 43 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.493+1512_493+1521d others(12): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783020 | ||||||
| chr12:46783020
|
A | ATGTGTGT others(5): Show |
7 | a0001c0001t0001g0209a0001c0001t0002g0271a0001c0001t0004g0312others(4): Show | 8 | HG01433.hp2 HG01496.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.493+1510_493+1521d others(14): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783020 | ||||||
| chr12:46783020
|
A | ATGTGTGT others(7): Show |
2 | a0001c0001t0005g0027a0001c0001t0005g0259 | 3 | HG01515.hp1 HG01517.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.493+1508_493+1521d others(16): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783020 | ||||||
| chr12:46783020
|
A | ATGTGTGT others(11): Show |
1 | a0001c0001t0001g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+1504_493+1521d others(20): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783020 | ||||||
| chr12:46783020
|
ATG | A | 9 | a0001c0005t0015g0052a0003c0003t0002g0247a0003c0003t0002g0273others(6): Show | 9 | HG01192.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.493+1520_493+1521d others(4): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783020 | ||||||
| chr12:46783050
|
G | GTGTGTGT others(1): Show |
3 | a0001c0001t0010g0169a0001c0001t0010g0171a0001c0001t0016g0172 | 3 | HG02257.hp1 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.493+1491_493+1492i others(10): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783050 | ||||||
| chr12:46783051
|
T | TGTGC | 3 | a0001c0001t0001g0117a0001c0001t0001g0151a0009c0014t0001g0224 | 3 | HG02129.hp2 HG02602.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.493+1490_493+1491i others(6): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783051 | ||||||
| chr12:46783051
|
T | TGTGTGC | 86 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(83): Show | 97 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.493+1490_493+1491i others(8): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783051 | ||||||
| chr12:46783051
|
T | TGTGTGTG others(1): Show |
14 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0039others(11): Show | 16 | HG01168.hp1 HG01256.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.493+1490_493+1491i others(10): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783051 | ||||||
| chr12:46783051
|
T | TGTGTGTG others(3): Show |
2 | a0001c0001t0001g0202a0001c0001t0008g0282 | 2 | HG02735.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.493+1490_493+1491i others(12): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783051 | ||||||
| chr12:46783051
|
T | TGTGTGTG others(5): Show |
3 | a0001c0001t0001g0198a0001c0001t0008g0279a0001c0001t0008g0280 | 3 | HG03041.hp1 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.493+1490_493+1491i others(14): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783051 | ||||||
| chr12:46783051
|
T | TGTGTGTG others(7): Show |
3 | a0001c0001t0001g0232a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | HG01081.hp1 HG01261.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.493+1490_493+1491i others(16): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783051 | ||||||
| chr12:46783051
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0233 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.493+1490_493+1491i others(18): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783051 | ||||||
| chr12:46783138
|
A | C | 1 | a0002c0002t0001g0087 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.493+1404T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783138 | ||||||
| chr12:46783227
|
T | TGATA | 83 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(80): Show | 92 | HG00280.hp1 HG00280.hp2 HG01081.hp2 others(89): Show |
intron_variant | MODIFIER | c.493+1311_493+1314d others(6): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783227 | ||||||
| chr12:46783227
|
T | TGATAGAT others(1): Show |
10 | a0001c0001t0001g0120a0001c0001t0001g0138a0001c0001t0001g0146others(7): Show | 10 | HG01261.hp1 HG02056.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.493+1307_493+1314d others(10): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783227 | ||||||
| chr12:46783227
|
T | TGATAGAT others(5): Show |
2 | a0001c0001t0001g0205a0001c0001t0001g0245 | 2 | HG04199.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.493+1303_493+1314d others(14): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783227 | ||||||
| chr12:46783227
|
TGATA | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0019others(60): Show | 69 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.493+1311_493+1314d others(6): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783227 | ||||||
| chr12:46783227
|
TGATAGAT others(1): Show |
T | 19 | a0001c0001t0001g0089a0001c0001t0003g0216a0001c0001t0004g0319others(16): Show | 26 | HG01192.hp1 HG02074.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.493+1307_493+1314d others(10): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783227 | ||||||
| chr12:46783227
|
TGATAGAT others(5): Show |
T | 4 | a0001c0001t0001g0011a0002c0002t0001g0055a0002c0002t0002g0008others(1): Show | 6 | HG00558.hp2 HG01109.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.493+1303_493+1314d others(14): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783227 | ||||||
| chr12:46783306
|
AG | A | 177 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(174): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.493+1235delC | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783306 | ||||||
| chr12:46783461
|
C | A | 18 | a0001c0001t0005g0027a0001c0001t0005g0036a0001c0001t0005g0037others(15): Show | 19 | HG01099.hp2 HG01515.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.493+1081G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783461 | ||||||
| chr12:46783569
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.493+973G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783569 | ||||||
| chr12:46783806
|
A | T | 1 | a0001c0001t0001g0180 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.493+736T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783806 | ||||||
| chr12:46783972
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.493+570G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783972 | ||||||
| chr12:46784024
|
G | A | 50 | a0001c0001t0001g0011a0003c0003t0002g0018a0003c0003t0002g0026others(47): Show | 58 | HG00673.hp1 HG01071.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.493+518C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46784024 | ||||||
| chr12:46784155
|
A | C | 177 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(174): Show | 196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.493+387T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46784155 | ||||||
| chr12:46784269
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0161 | 2 | HG01256.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.493+273C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46784269 | ||||||
| chr12:46784382
|
A | G | 2 | a0002c0002t0012g0074a0002c0002t0013g0104 | 2 | HG00642.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.493+160T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46784382 | ||||||
| chr12:46784496
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.493+46G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46784496 | ||||||
| chr12:46784524
|
A | G | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(173): Show | 195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.493+18T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46784524 | ||||||
| chr12:46785296
|
G | A | 1 | a0002c0002t0002g0051 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.327-119C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785296 | ||||||
| chr12:46785399
|
C | CTT | 339 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(336): Show | 383 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(380): Show |
intron_variant | MODIFIER | c.327-224_327-223dup others(2): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785399 | ||||||
| chr12:46785471
|
T | C | 6 | a0001c0001t0001g0031a0001c0001t0002g0290a0001c0001t0002g0301others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.327-294A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785471 | ||||||
| chr12:46785534
|
A | G | 250 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(247): Show | 280 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.327-357T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785534 | ||||||
| chr12:46785563
|
C | T | 1 | a0001c0001t0004g0330 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.327-386G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785563 | ||||||
| chr12:46785590
|
G | A | 1 | a0002c0002t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.327-413C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785590 | ||||||
| chr12:46785702
|
A | AAAGCAG | 3 | a0001c0001t0001g0029a0001c0001t0001g0275a0001c0005t0001g0305 | 4 | HG02257.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-531_327-526dup others(6): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785702 | ||||||
| chr12:46785720
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.327-543C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785720 | ||||||
| chr12:46785736
|
T | TC | 5 | a0001c0001t0002g0295a0001c0001t0006g0333a0002c0002t0002g0059others(2): Show | 5 | HG02056.hp1 HG02451.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.327-560dupG | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785736 | ||||||
| chr12:46785738
|
C | CCTTT | 3 | a0001c0001t0010g0169a0001c0001t0010g0171a0001c0001t0016g0172 | 3 | HG02257.hp1 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.327-562_327-561ins others(4): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785738 | ||||||
| chr12:46785738
|
CT | C | 227 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(224): Show | 257 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.327-562delA | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785738 | ||||||
| chr12:46785738
|
CTT | C | 6 | a0001c0001t0001g0184a0001c0001t0001g0221a0001c0001t0005g0044others(3): Show | 6 | HG00673.hp1 HG02698.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-563_327-562del others(2): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785738 | ||||||
| chr12:46785738
|
CTTTTTTT others(1): Show |
C | 13 | a0001c0001t0001g0030a0001c0001t0001g0294a0001c0001t0003g0291others(10): Show | 14 | HG02258.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.327-569_327-562del others(8): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785738 | ||||||
| chr12:46785738
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.327-571_327-562del others(10): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785738 | ||||||
| chr12:46785739
|
T | C | 40 | a0001c0001t0001g0092a0001c0001t0001g0178a0001c0001t0001g0188others(37): Show | 49 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.327-562A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785739 | ||||||
| chr12:46785740
|
T | C | 49 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 56 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.327-563A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785740 | ||||||
| chr12:46785741
|
T | C | 2 | a0001c0001t0001g0184a0003c0003t0002g0208 | 2 | HG03516.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.327-564A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785741 | ||||||
| chr12:46785743
|
T | C | 1 | a0003c0003t0002g0285 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.327-566A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785743 | ||||||
| chr12:46785774
|
T | C | 48 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(45): Show | 55 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.327-597A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785774 | ||||||
| chr12:46785791
|
C | T | 46 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(43): Show | 53 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.327-614G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785791 | ||||||
| chr12:46785893
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.327-716C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785893 | ||||||
| chr12:46786011
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0294 | 3 | HG02630.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.327-834G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46786011 | ||||||
| chr12:46786100
|
G | A | 1 | a0002c0002t0002g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.327-923C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46786100 | ||||||
| chr12:46786225
|
A | G | 26 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(23): Show | 28 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(25): Show |
intron_variant | MODIFIER | c.327-1048T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46786225 | ||||||
| chr12:46786317
|
T | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.327-1140A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46786317 | ||||||
| chr12:46786587
|
C | G | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(166): Show | 188 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.326+1329G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46786587 | ||||||
| chr12:46786629
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0137 | 2 | NA18953.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.326+1287T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46786629 | ||||||
| chr12:46786699
|
A | C | 64 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(61): Show | 71 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(68): Show |
intron_variant | MODIFIER | c.326+1217T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46786699 | ||||||
| chr12:46786709
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.326+1207T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46786709 | ||||||
| chr12:46786729
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.326+1187A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46786729 | ||||||
| chr12:46786747
|
T | G | 1 | a0001c0001t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.326+1169A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46786747 | ||||||
| chr12:46786773
|
T | C | 1 | a0001c0005t0001g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.326+1143A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46786773 | ||||||
| chr12:46787098
|
A | T | 19 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(16): Show | 21 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.326+818T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46787098 | ||||||
| chr12:46787151
|
T | C | 47 | a0002c0002t0001g0010a0002c0002t0001g0053a0002c0002t0001g0054others(44): Show | 61 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.326+765A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46787151 | ||||||
| chr12:46787217
|
G | C | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.326+699C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46787217 | ||||||
| chr12:46787391
|
T | G | 64 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(61): Show | 71 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(68): Show |
intron_variant | MODIFIER | c.326+525A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46787391 | ||||||
| chr12:46787505
|
G | A | 2 | a0003c0003t0002g0222a0003c0003t0002g0223 | 2 | NA18953.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.326+411C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46787505 | ||||||
| chr12:46787542
|
G | C | 19 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(16): Show | 21 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.326+374C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46787542 | ||||||
| chr12:46787631
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0118a0001c0001t0003g0093others(2): Show | 6 | HG01109.hp2 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.326+285T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46787631 | ||||||
| chr12:46787689
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.326+227T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46787689 | ||||||
| chr12:46787730
|
C | G | 22 | a0001c0001t0001g0321a0001c0001t0003g0318a0001c0001t0004g0006others(19): Show | 26 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.326+186G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46787730 | ||||||
| chr12:46788312
|
T | C | 1 | a0001c0005t0001g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.210+216A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 4/16 | chr12 | 46788312 | ||||||
| chr12:46788496
|
C | T | 47 | a0002c0002t0001g0010a0002c0002t0001g0053a0002c0002t0001g0054others(44): Show | 61 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.210+32G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 4/16 | chr12 | 46788496 | ||||||
| chr12:46788622
|
A | AAC | 49 | a0002c0002t0001g0010a0002c0002t0001g0053a0002c0002t0001g0054others(46): Show | 63 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(60): Show |
splice_region_variant&intron_variant | LOW | c.120-6_120-5dupGT | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46788622 | ||||||
| chr12:46788665
|
A | G | 7 | a0001c0001t0001g0031a0001c0001t0001g0303a0001c0001t0001g0307others(4): Show | 8 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.120-47T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46788665 | ||||||
| chr12:46788682
|
T | C | 1 | a0002c0002t0013g0104 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.120-64A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46788682 | ||||||
| chr12:46788718
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.120-100C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46788718 | ||||||
| chr12:46788748
|
C | T | 19 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(16): Show | 21 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.120-130G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46788748 | ||||||
| chr12:46788757
|
A | G | 25 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0294others(22): Show | 27 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.120-139T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46788757 | ||||||
| chr12:46788842
|
A | T | 1 | a0003c0003t0002g0283 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.120-224T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46788842 | ||||||
| chr12:46788951
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120-333C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46788951 | ||||||
| chr12:46788988
|
C | G | 2 | a0003c0003t0002g0247a0007c0009t0002g0248 | 2 | HG01192.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.120-370G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46788988 | ||||||
| chr12:46789208
|
C | CT | 8 | a0001c0001t0003g0143a0001c0001t0003g0195a0001c0001t0003g0206others(5): Show | 8 | HG00673.hp1 HG01192.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.120-591dupA | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46789208 | ||||||
| chr12:46789208
|
CT | C | 50 | a0001c0001t0001g0105a0001c0001t0006g0335a0001c0001t0006g0338others(47): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.120-591delA | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46789208 | ||||||
| chr12:46789271
|
A | T | 1 | a0003c0003t0002g0028 | 2 | NA19009.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.120-653T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46789271 | ||||||
| chr12:46789579
|
G | A | 2 | a0001c0005t0001g0167a0011c0017t0002g0168 | 2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.120-961C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46789579 | ||||||
| chr12:46789623
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120-1005G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46789623 | ||||||
| chr12:46789632
|
G | T | 49 | a0002c0002t0001g0010a0002c0002t0001g0053a0002c0002t0001g0054others(46): Show | 63 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.120-1014C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46789632 | ||||||
| chr12:46789647
|
G | C | 2 | a0003c0003t0002g0247a0007c0009t0002g0248 | 2 | HG01192.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.120-1029C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46789647 | ||||||
| chr12:46789666
|
C | T | 1 | a0001c0005t0015g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.120-1048G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46789666 | ||||||
| chr12:46789679
|
A | G | 332 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(329): Show | 376 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(373): Show |
intron_variant | MODIFIER | c.120-1061T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46789679 | ||||||
| chr12:46789870
|
A | C | 1 | a0002c0002t0002g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.120-1252T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46789870 | ||||||
| chr12:46789964
|
G | A | 64 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(61): Show | 71 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(68): Show |
intron_variant | MODIFIER | c.120-1346C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46789964 | ||||||
| chr12:46790040
|
T | C | 1 | a0001c0001t0006g0333 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.120-1422A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46790040 | ||||||
| chr12:46790070
|
CTCTG | C | 65 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(62): Show | 72 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(69): Show |
intron_variant | MODIFIER | c.120-1456_120-1453d others(6): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46790070 | ||||||
| chr12:46790259
|
C | T | 83 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0039others(80): Show | 92 | HG00408.hp2 HG00673.hp1 HG01099.hp2 others(89): Show |
intron_variant | MODIFIER | c.120-1641G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46790259 | ||||||
| chr12:46790412
|
C | T | 4 | a0001c0001t0008g0279a0001c0001t0008g0280a0001c0001t0008g0282others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.120-1794G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46790412 | ||||||
| chr12:46790751
|
TA | T | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0202others(1): Show | 4 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.120-2134delT | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46790751 | ||||||
| chr12:46790753
|
G | C | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0202others(1): Show | 4 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.120-2135C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46790753 | ||||||
| chr12:46790782
|
T | TTTTGATA others(38): Show |
1 | a0007c0009t0002g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.120-2165_120-2164i others(47): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46790782 | ||||||
| chr12:46790948
|
ATGTT | A | 42 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(39): Show | 45 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.119+2001_119+2004d others(6): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46790948 | ||||||
| chr12:46791000
|
T | C | 64 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(61): Show | 71 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(68): Show |
intron_variant | MODIFIER | c.119+1953A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791000 | ||||||
| chr12:46791114
|
C | T | 9 | a0001c0001t0001g0031a0001c0001t0001g0303a0001c0001t0001g0304others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.119+1839G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791114 | ||||||
| chr12:46791135
|
G | T | 25 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0294others(22): Show | 27 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.119+1818C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791135 | ||||||
| chr12:46791284
|
T | C | 1 | a0002c0002t0002g0056 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.119+1669A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791284 | ||||||
| chr12:46791304
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.119+1649C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791304 | ||||||
| chr12:46791311
|
C | G | 55 | a0001c0005t0001g0305a0002c0002t0001g0010a0002c0002t0001g0053others(52): Show | 69 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.119+1642G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791311 | ||||||
| chr12:46791362
|
C | G | 1 | a0002c0002t0002g0038 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.119+1591G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791362 | ||||||
| chr12:46791488
|
G | C | 119 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(116): Show | 140 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.119+1465C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791488 | ||||||
| chr12:46791634
|
G | T | 64 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(61): Show | 71 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(68): Show |
intron_variant | MODIFIER | c.119+1319C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791634 | ||||||
| chr12:46791639
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.119+1314T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791639 | ||||||
| chr12:46791686
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.119+1267G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791686 | ||||||
| chr12:46791735
|
C | T | 19 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(16): Show | 21 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.119+1218G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791735 | ||||||
| chr12:46791881
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.119+1072C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791881 | ||||||
| chr12:46791904
|
G | A | 1 | a0002c0002t0012g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.119+1049C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791904 | ||||||
| chr12:46791948
|
G | C | 19 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(16): Show | 21 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.119+1005C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46791948 | ||||||
| chr12:46792025
|
A | T | 1 | a0001c0001t0001g0015 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.119+928T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46792025 | ||||||
| chr12:46792176
|
A | T | 22 | a0001c0001t0001g0321a0001c0001t0003g0318a0001c0001t0004g0006others(19): Show | 26 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.119+777T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46792176 | ||||||
| chr12:46792180
|
C | T | 54 | a0002c0002t0001g0010a0002c0002t0001g0053a0002c0002t0001g0054others(51): Show | 68 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.119+773G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46792180 | ||||||
| chr12:46792221
|
C | T | 1 | a0002c0002t0013g0104 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.119+732G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46792221 | ||||||
| chr12:46792477
|
A | G | 138 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0039others(135): Show | 161 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.119+476T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46792477 | ||||||
| chr12:46792486
|
T | C | 1 | a0001c0005t0015g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.119+467A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46792486 | ||||||
| chr12:46792653
|
T | C | 1 | a0001c0005t0001g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.119+300A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46792653 | ||||||
| chr12:46792696
|
A | G | 4 | a0001c0001t0003g0143a0001c0001t0003g0195a0001c0001t0003g0206others(1): Show | 4 | NA18747.hp1 NA18967.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+257T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46792696 | ||||||
| chr12:46792925
|
T | C | 13 | a0001c0001t0001g0031a0001c0001t0001g0303a0001c0001t0001g0304others(10): Show | 14 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.119+28A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 3/16 | chr12 | 46792925 | ||||||
| chr12:46793251
|
T | C | 1 | a0003c0003t0002g0268 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-112-68A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46793251 | ||||||
| chr12:46793314
|
A | C | 331 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(328): Show | 375 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(372): Show |
intron_variant | MODIFIER | c.-112-131T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46793314 | ||||||
| chr12:46793374
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-112-191T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46793374 | ||||||
| chr12:46793477
|
G | A | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(154): Show | 175 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.-112-294C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46793477 | ||||||
| chr12:46793605
|
C | T | 54 | a0002c0002t0001g0010a0002c0002t0001g0053a0002c0002t0001g0054others(51): Show | 68 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-112-422G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46793605 | ||||||
| chr12:46793680
|
T | A | 12 | a0001c0001t0001g0030a0001c0001t0001g0294a0001c0001t0002g0295others(9): Show | 13 | HG02258.hp2 HG02451.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-112-497A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46793680 | ||||||
| chr12:46793706
|
G | C | 1 | a0001c0001t0001g0160 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-112-523C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46793706 | ||||||
| chr12:46793749
|
G | A | 52 | a0002c0002t0001g0010a0002c0002t0001g0053a0002c0002t0001g0054others(49): Show | 66 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-112-566C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46793749 | ||||||
| chr12:46793879
|
T | C | 2 | a0001c0001t0005g0189a0009c0014t0001g0224 | 2 | HG02602.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-112-696A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46793879 | ||||||
| chr12:46793911
|
G | A | 19 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(16): Show | 21 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.-112-728C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46793911 | ||||||
| chr12:46793933
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-112-750T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46793933 | ||||||
| chr12:46794056
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0265 | 2 | HG03491.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-112-873C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46794056 | ||||||
| chr12:46794189
|
A | G | 2 | a0002c0002t0012g0074a0002c0002t0013g0104 | 2 | HG00642.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-112-1006T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46794189 | ||||||
| chr12:46794299
|
A | G | 119 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(116): Show | 140 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-112-1116T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46794299 | ||||||
| chr12:46794318
|
A | T | 52 | a0002c0002t0001g0010a0002c0002t0001g0053a0002c0002t0001g0054others(49): Show | 66 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-112-1135T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46794318 | ||||||
| chr12:46794360
|
T | A | 1 | a0001c0001t0003g0243 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-112-1177A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46794360 | ||||||
| chr12:46794394
|
T | A | 1 | a0001c0001t0006g0333 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-112-1211A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46794394 | ||||||
| chr12:46794410
|
C | T | 1 | a0002c0002t0002g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-112-1227G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46794410 | ||||||
| chr12:46794650
|
C | G | 19 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(16): Show | 21 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.-112-1467G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46794650 | ||||||
| chr12:46794685
|
A | G | 64 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(61): Show | 71 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(68): Show |
intron_variant | MODIFIER | c.-112-1502T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46794685 | ||||||
| chr12:46794726
|
A | T | 1 | a0001c0001t0001g0262 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-112-1543T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46794726 | ||||||
| chr12:46795184
|
A | AT | 4 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0042others(1): Show | 5 | NA18948.hp1 NA18969.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112-2002dupA | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46795184 | ||||||
| chr12:46795392
|
T | C | 1 | a0004c0004t0002g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-112-2209A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46795392 | ||||||
| chr12:46795512
|
C | T | 55 | a0001c0005t0001g0305a0002c0002t0001g0010a0002c0002t0001g0053others(52): Show | 69 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-112-2329G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46795512 | ||||||
| chr12:46795669
|
T | G | 1 | a0001c0001t0002g0162 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-112-2486A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46795669 | ||||||
| chr12:46795765
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-112-2582G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46795765 | ||||||
| chr12:46795830
|
AT | A | 52 | a0002c0002t0001g0010a0002c0002t0001g0053a0002c0002t0001g0054others(49): Show | 66 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-112-2648delA | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46795830 | ||||||
| chr12:46795919
|
C | CCATT | 138 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0039others(135): Show | 161 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.-112-2737_-112-273 others(8): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46795919 | ||||||
| chr12:46795924
|
C | A | 1 | a0003c0003t0002g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-112-2741G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46795924 | ||||||
| chr12:46796029
|
T | C | 1 | a0001c0005t0001g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-112-2846A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796029 | ||||||
| chr12:46796034
|
A | G | 1 | a0001c0001t0001g0015 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.-112-2851T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796034 | ||||||
| chr12:46796144
|
T | C | 1 | a0001c0005t0001g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-112-2961A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796144 | ||||||
| chr12:46796278
|
G | A | 52 | a0002c0002t0001g0010a0002c0002t0001g0053a0002c0002t0001g0054others(49): Show | 66 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-112-3095C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796278 | ||||||
| chr12:46796310
|
A | T | 1 | a0001c0001t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-112-3127T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796310 | ||||||
| chr12:46796449
|
T | C | 1 | a0002c0002t0013g0104 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-112-3266A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796449 | ||||||
| chr12:46796473
|
C | T | 25 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0294others(22): Show | 27 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.-112-3290G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796473 | ||||||
| chr12:46796646
|
G | A | 1 | a0001c0005t0001g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-112-3463C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796646 | ||||||
| chr12:46796665
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | NA18948.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-112-3482C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796665 | ||||||
| chr12:46796695
|
T | C | 19 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(16): Show | 21 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.-112-3512A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796695 | ||||||
| chr12:46796745
|
C | T | 1 | a0002c0002t0013g0104 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-112-3562G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796745 | ||||||
| chr12:46796752
|
CCTTGAGG others(3): Show |
C | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(162): Show | 184 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(181): Show |
intron_variant | MODIFIER | c.-112-3579_-112-357 others(14): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796752 | ||||||
| chr12:46796759
|
G | A | 5 | a0001c0001t0001g0031a0001c0001t0002g0290a0001c0001t0002g0301others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112-3576C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796759 | ||||||
| chr12:46796900
|
G | A | 19 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(16): Show | 21 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.-112-3717C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796900 | ||||||
| chr12:46796954
|
G | A | 1 | a0002c0002t0002g0073 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-112-3771C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796954 | ||||||
| chr12:46796983
|
A | G | 52 | a0002c0002t0001g0010a0002c0002t0001g0053a0002c0002t0001g0054others(49): Show | 66 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-112-3800T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46796983 | ||||||
| chr12:46797162
|
G | A | 201 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(198): Show | 222 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(219): Show |
intron_variant | MODIFIER | c.-112-3979C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797162 | ||||||
| chr12:46797214
|
G | C | 1 | a0002c0002t0002g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-112-4031C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797214 | ||||||
| chr12:46797323
|
G | C | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-112-4140C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797323 | ||||||
| chr12:46797387
|
C | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0265 | 2 | HG03491.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-112-4204G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797387 | ||||||
| chr12:46797411
|
C | T | 1 | a0001c0001t0003g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-112-4228G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797411 | ||||||
| chr12:46797572
|
G | A | 13 | a0001c0001t0001g0031a0001c0001t0001g0303a0001c0001t0001g0304others(10): Show | 14 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-112-4389C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797572 | ||||||
| chr12:46797620
|
T | A | 1 | a0001c0001t0002g0258 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-112-4437A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797620 | ||||||
| chr12:46797697
|
T | C | 337 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(334): Show | 381 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(378): Show |
intron_variant | MODIFIER | c.-112-4514A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797697 | ||||||
| chr12:46797709
|
C | T | 19 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(16): Show | 21 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.-112-4526G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797709 | ||||||
| chr12:46797777
|
C | T | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(162): Show | 184 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(181): Show |
intron_variant | MODIFIER | c.-112-4594G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797777 | ||||||
| chr12:46797787
|
T | A | 1 | a0008c0013t0001g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-112-4604A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797787 | ||||||
| chr12:46797902
|
C | A | 42 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(39): Show | 45 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.-112-4719G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797902 | ||||||
| chr12:46798100
|
A | G | 25 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0294others(22): Show | 27 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.-112-4917T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46798100 | ||||||
| chr12:46798320
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-112-5137G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46798320 | ||||||
| chr12:46798540
|
A | G | 337 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(334): Show | 381 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(378): Show |
intron_variant | MODIFIER | c.-113+5063T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46798540 | ||||||
| chr12:46798640
|
A | G | 2 | a0001c0005t0001g0167a0011c0017t0002g0168 | 2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-113+4963T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46798640 | ||||||
| chr12:46798656
|
T | C | 6 | a0001c0001t0001g0088a0001c0001t0006g0335a0001c0001t0006g0336others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-113+4947A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46798656 | ||||||
| chr12:46798773
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-113+4830C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46798773 | ||||||
| chr12:46798816
|
G | A | 2 | a0005c0006t0001g0077a0005c0006t0001g0078 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-113+4787C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46798816 | ||||||
| chr12:46798935
|
C | G | 1 | a0003c0003t0002g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-113+4668G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46798935 | ||||||
| chr12:46798958
|
T | C | 74 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0255others(71): Show | 82 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(79): Show |
intron_variant | MODIFIER | c.-113+4645A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46798958 | ||||||
| chr12:46799365
|
G | T | 19 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(16): Show | 21 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.-113+4238C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46799365 | ||||||
| chr12:46799535
|
T | G | 1 | a0001c0001t0003g0231 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-113+4068A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46799535 | ||||||
| chr12:46799583
|
A | T | 1 | a0001c0001t0001g0142 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-113+4020T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46799583 | ||||||
| chr12:46799614
|
T | G | 1 | a0001c0005t0001g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-113+3989A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46799614 | ||||||
| chr12:46799773
|
A | T | 1 | a0002c0002t0002g0165 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-113+3830T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46799773 | ||||||
| chr12:46799817
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0209 | 2 | HG01123.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-113+3786A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46799817 | ||||||
| chr12:46800035
|
C | T | 191 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(188): Show | 211 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.-113+3568G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800035 | ||||||
| chr12:46800094
|
G | T | 9 | a0001c0001t0001g0031a0001c0001t0001g0303a0001c0001t0001g0304others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-113+3509C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800094 | ||||||
| chr12:46800277
|
G | A | 3 | a0001c0005t0001g0167a0001c0005t0015g0052a0011c0017t0002g0168 | 3 | HG02145.hp2 HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-113+3326C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800277 | ||||||
| chr12:46800283
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0006g0335a0001c0001t0006g0336others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-113+3320C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800283 | ||||||
| chr12:46800283
|
G | C | 52 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0255others(49): Show | 56 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(53): Show |
intron_variant | MODIFIER | c.-113+3320C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800283 | ||||||
| chr12:46800362
|
A | G | 4 | a0001c0001t0008g0279a0001c0001t0008g0280a0001c0001t0008g0282others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113+3241T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800362 | ||||||
| chr12:46800380
|
C | T | 1 | a0003c0003t0002g0278 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-113+3223G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800380 | ||||||
| chr12:46800545
|
A | C | 1 | a0003c0003t0002g0317 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-113+3058T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800545 | ||||||
| chr12:46800568
|
A | G | 4 | a0001c0001t0001g0090a0001c0001t0001g0103a0001c0001t0001g0129others(1): Show | 4 | NA18965.hp1 NA18987.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113+3035T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800568 | ||||||
| chr12:46800638
|
C | A | 1 | a0002c0002t0002g0082 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-113+2965G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800638 | ||||||
| chr12:46800905
|
C | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(15): Show | 20 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.-113+2698G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800905 | ||||||
| chr12:46800930
|
G | T | 2 | a0001c0001t0005g0210a0001c0001t0005g0211 | 2 | NA19012.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.-113+2673C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800930 | ||||||
| chr12:46800949
|
G | A | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 212 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.-113+2654C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800949 | ||||||
| chr12:46800974
|
T | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(15): Show | 20 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.-113+2629A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800974 | ||||||
| chr12:46801100
|
G | A | 1 | a0002c0002t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-113+2503C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801100 | ||||||
| chr12:46801112
|
A | G | 1 | a0001c0005t0001g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-113+2491T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801112 | ||||||
| chr12:46801122
|
C | A | 166 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(163): Show | 185 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.-113+2481G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801122 | ||||||
| chr12:46801273
|
G | C | 18 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(15): Show | 20 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.-113+2330C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801273 | ||||||
| chr12:46801407
|
C | T | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231 | 3 | HG00423.hp1 NA19070.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-113+2196G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801407 | ||||||
| chr12:46801408
|
G | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(15): Show | 20 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.-113+2195C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801408 | ||||||
| chr12:46801506
|
C | T | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 212 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.-113+2097G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801506 | ||||||
| chr12:46801632
|
A | G | 18 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(15): Show | 20 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.-113+1971T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801632 | ||||||
| chr12:46801684
|
C | G | 3 | a0001c0005t0001g0167a0001c0005t0015g0052a0011c0017t0002g0168 | 3 | HG02145.hp2 HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-113+1919G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801684 | ||||||
| chr12:46801761
|
T | C | 15 | a0001c0001t0001g0031a0001c0001t0001g0303a0001c0001t0001g0304others(12): Show | 16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-113+1842A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801761 | ||||||
| chr12:46801947
|
G | A | 1 | a0003c0003t0002g0285 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-113+1656C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801947 | ||||||
| chr12:46802076
|
A | T | 2 | a0001c0001t0002g0271a0003c0003t0002g0270 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-113+1527T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802076 | ||||||
| chr12:46802271
|
A | G | 2 | a0001c0001t0002g0295a0001c0001t0006g0333 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-113+1332T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802271 | ||||||
| chr12:46802451
|
T | G | 1 | a0002c0002t0001g0087 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-113+1152A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802451 | ||||||
| chr12:46802481
|
A | C | 1 | a0001c0001t0001g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-113+1122T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802481 | ||||||
| chr12:46802606
|
T | A | 1 | a0001c0005t0015g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-113+997A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802606 | ||||||
| chr12:46802606
|
T | C | 284 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(281): Show | 314 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(311): Show |
intron_variant | MODIFIER | c.-113+997A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802606 | ||||||
| chr12:46802678
|
C | T | 285 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(282): Show | 315 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(312): Show |
intron_variant | MODIFIER | c.-113+925G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802678 | ||||||
| chr12:46802722
|
A | G | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 212 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.-113+881T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802722 | ||||||
| chr12:46802743
|
T | C | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | NA18962.hp1 NA19057.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-113+860A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802743 | ||||||
| chr12:46802848
|
A | G | 18 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(15): Show | 20 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.-113+755T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802848 | ||||||
| chr12:46802907
|
G | A | 52 | a0002c0002t0001g0010a0002c0002t0001g0053a0002c0002t0001g0054others(49): Show | 66 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-113+696C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802907 | ||||||
| chr12:46803263
|
G | C | 1 | a0001c0001t0001g0141 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-113+340C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46803263 | ||||||
| chr12:46803265
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-113+338G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46803265 | ||||||
| chr12:46803267
|
A | C | 1 | a0001c0001t0001g0141 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-113+336T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46803267 | ||||||
| chr12:46803268
|
T | A | 1 | a0001c0001t0001g0141 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-113+335A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46803268 | ||||||
| chr12:46803270
|
C | A | 1 | a0001c0001t0001g0141 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-113+333G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46803270 | ||||||
| chr12:46803271
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-113+332A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46803271 | ||||||
| chr12:46803273
|
C | G | 1 | a0001c0001t0001g0141 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-113+330G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46803273 | ||||||
| chr12:46803276
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-113+327A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46803276 | ||||||
| chr12:46803277
|
A | T | 1 | a0001c0001t0001g0141 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-113+326T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46803277 | ||||||
| chr12:46803288
|
T | C | 1 | a0001c0001t0001g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-113+315A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46803288 | ||||||
| chr12:46803526
|
TAAAC | T | 3 | a0001c0005t0001g0167a0001c0005t0015g0052a0011c0017t0002g0168 | 3 | HG02145.hp2 HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-113+73_-113+76del others(4): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46803526 | ||||||
| chr12:46803536
|
A | C | 1 | a0001c0001t0001g0209 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-113+67T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46803536 | ||||||
| chr12:46803865
|
A | G | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 212 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.-304-71T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46803865 | ||||||
| chr12:46803994
|
G | A | 1 | a0004c0004t0002g0201 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-304-200C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46803994 | ||||||
| chr12:46804020
|
T | C | 74 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0255others(71): Show | 82 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(79): Show |
intron_variant | MODIFIER | c.-304-226A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46804020 | ||||||
| chr12:46804056
|
T | C | 18 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(15): Show | 20 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.-304-262A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46804056 | ||||||
| chr12:46804130
|
A | G | 337 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(334): Show | 381 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(378): Show |
intron_variant | MODIFIER | c.-304-336T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46804130 | ||||||
| chr12:46804192
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-304-398T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46804192 | ||||||
| chr12:46804477
|
C | T | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 212 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.-304-683G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46804477 | ||||||
| chr12:46804534
|
C | T | 1 | a0001c0001t0003g0291 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-304-740G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46804534 | ||||||
| chr12:46804805
|
G | T | 15 | a0001c0001t0001g0031a0001c0001t0001g0303a0001c0001t0001g0304others(12): Show | 16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-304-1011C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46804805 | ||||||
| chr12:46804807
|
C | T | 5 | a0001c0001t0005g0036a0001c0001t0005g0037a0001c0001t0005g0040others(2): Show | 5 | HG01099.hp2 HG01516.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-304-1013G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46804807 | ||||||
| chr12:46804876
|
C | A | 1 | a0001c0001t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-304-1082G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46804876 | ||||||
| chr12:46804926
|
T | C | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 212 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.-304-1132A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46804926 | ||||||
| chr12:46805053
|
C | T | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 212 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.-304-1259G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805053 | ||||||
| chr12:46805073
|
C | A | 17 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(14): Show | 19 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.-304-1279G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805073 | ||||||
| chr12:46805112
|
A | C | 3 | a0001c0001t0010g0169a0001c0001t0010g0171a0001c0001t0016g0172 | 3 | HG02257.hp1 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-304-1318T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805112 | ||||||
| chr12:46805116
|
C | A | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 212 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.-304-1322G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805116 | ||||||
| chr12:46805152
|
C | T | 1 | a0001c0001t0002g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-304-1358G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805152 | ||||||
| chr12:46805197
|
T | G | 1 | a0011c0017t0002g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-304-1403A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805197 | ||||||
| chr12:46805383
|
A | C | 2 | a0001c0001t0002g0295a0001c0001t0006g0333 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-304-1589T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805383 | ||||||
| chr12:46805565
|
A | C | 8 | a0001c0001t0001g0019a0001c0001t0001g0175a0001c0001t0001g0176others(5): Show | 10 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-304-1771T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805565 | ||||||
| chr12:46805589
|
A | G | 2 | a0001c0005t0001g0167a0011c0017t0002g0168 | 2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-304-1795T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805589 | ||||||
| chr12:46805695
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-304-1901T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805695 | ||||||
| chr12:46805766
|
G | A | 13 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0047others(10): Show | 14 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.-304-1972C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805766 | ||||||
| chr12:46805868
|
T | A | 17 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0041others(14): Show | 19 | HG01099.hp2 HG01361.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.-304-2074A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805868 | ||||||
| chr12:46805963
|
T | C | 1 | a0003c0003t0002g0317 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-304-2169A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805963 | ||||||
| chr12:46806096
|
G | A | 1 | a0009c0014t0001g0224 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-304-2302C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46806096 | ||||||
| chr12:46806165
|
A | C | 10 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0002g0295others(7): Show | 10 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-304-2371T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46806165 | ||||||
| chr12:46806185
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-304-2391A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46806185 | ||||||
| chr12:46806413
|
A | T | 1 | a0001c0001t0002g0295 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-304-2619T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46806413 | ||||||
| chr12:46806834
|
A | G | 34 | a0001c0001t0001g0092a0001c0001t0001g0321a0001c0001t0001g0328others(31): Show | 39 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.-304-3040T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46806834 | ||||||
| chr12:46806879
|
G | A | 292 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(289): Show | 321 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(318): Show |
intron_variant | MODIFIER | c.-304-3085C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46806879 | ||||||
| chr12:46807065
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-304-3271C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807065 | ||||||
| chr12:46807104
|
C | T | 2 | a0003c0003t0002g0247a0007c0009t0002g0248 | 2 | HG01192.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-304-3310G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807104 | ||||||
| chr12:46807137
|
G | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0265 | 2 | HG03491.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-304-3343C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807137 | ||||||
| chr12:46807216
|
T | G | 64 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0088others(61): Show | 69 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(66): Show |
intron_variant | MODIFIER | c.-304-3422A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807216 | ||||||
| chr12:46807336
|
T | C | 1 | a0002c0002t0002g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-304-3542A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807336 | ||||||
| chr12:46807362
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-304-3568C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807362 | ||||||
| chr12:46807380
|
G | A | 26 | a0001c0001t0001g0092a0001c0001t0001g0321a0001c0001t0001g0328others(23): Show | 30 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-304-3586C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807380 | ||||||
| chr12:46807471
|
C | A | 1 | a0002c0002t0002g0075 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-304-3677G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807471 | ||||||
| chr12:46807624
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-304-3830A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807624 | ||||||
| chr12:46807869
|
A | G | 26 | a0001c0001t0001g0092a0001c0001t0001g0321a0001c0001t0001g0328others(23): Show | 30 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-304-4075T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807869 | ||||||
| chr12:46807889
|
A | AC | 43 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(40): Show | 47 | HG00642.hp2 HG00735.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.-304-4096dupG | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807889 | ||||||
| chr12:46807889
|
AC | A | 171 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0015others(168): Show | 200 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.-304-4096delG | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807889 | ||||||
| chr12:46807889
|
ACC | A | 38 | a0001c0001t0001g0092a0001c0001t0001g0261a0001c0001t0001g0321others(35): Show | 44 | HG00280.hp1 HG00408.hp1 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.-304-4097_-304-409 others(6): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807889 | ||||||
| chr12:46807983
|
T | A | 1 | a0001c0001t0005g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-304-4189A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807983 | ||||||
| chr12:46808031
|
A | G | 145 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(142): Show | 173 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-304-4237T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46808031 | ||||||
| chr12:46808122
|
A | G | 6 | a0001c0001t0010g0169a0001c0001t0010g0171a0001c0001t0016g0172others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-304-4328T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46808122 | ||||||
| chr12:46808228
|
C | T | 3 | a0001c0001t0002g0290a0001c0001t0002g0295a0001c0001t0003g0292 | 3 | HG02451.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-304-4434G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46808228 | ||||||
| chr12:46808373
|
T | G | 1 | a0001c0001t0003g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-304-4579A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46808373 | ||||||
| chr12:46808499
|
G | T | 3 | a0001c0001t0001g0128a0001c0001t0001g0139a0001c0001t0001g0173 | 3 | HG00733.hp2 NA18978.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-304-4705C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46808499 | ||||||
| chr12:46808523
|
T | TA | 225 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(222): Show | 258 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.-304-4730dupT | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46808523 | ||||||
| chr12:46808612
|
C | G | 15 | a0001c0001t0003g0318a0001c0001t0004g0006a0001c0001t0004g0311others(12): Show | 17 | HG02074.hp1 HG02523.hp1 NA18961.hp2 others(14): Show |
intron_variant | MODIFIER | c.-304-4818G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46808612 | ||||||
| chr12:46808613
|
A | G | 4 | a0001c0001t0003g0195a0001c0001t0003g0206a0001c0001t0017g0196others(1): Show | 4 | HG00621.hp1 NA18967.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.-304-4819T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46808613 | ||||||
| chr12:46808668
|
G | A | 26 | a0001c0001t0001g0092a0001c0001t0001g0321a0001c0001t0001g0328others(23): Show | 30 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-304-4874C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46808668 | ||||||
| chr12:46808728
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0199a0001c0001t0001g0200 | 5 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(2): Show |
intron_variant | MODIFIER | c.-304-4934T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46808728 | ||||||
| chr12:46809017
|
C | T | 64 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0088others(61): Show | 69 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(66): Show |
intron_variant | MODIFIER | c.-304-5223G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46809017 | ||||||
| chr12:46809368
|
A | C | 1 | a0001c0001t0001g0257 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-304-5574T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46809368 | ||||||
| chr12:46809370
|
T | C | 6 | a0001c0001t0010g0169a0001c0001t0010g0171a0001c0001t0016g0172others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-304-5576A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46809370 | ||||||
| chr12:46809525
|
A | G | 1 | a0003c0003t0002g0272 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-304-5731T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46809525 | ||||||
| chr12:46809626
|
C | T | 253 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(250): Show | 290 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.-304-5832G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46809626 | ||||||
| chr12:46809713
|
A | G | 26 | a0001c0001t0001g0092a0001c0001t0001g0321a0001c0001t0001g0328others(23): Show | 30 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-304-5919T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46809713 | ||||||
| chr12:46809717
|
A | G | 88 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(85): Show | 101 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-304-5923T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46809717 | ||||||
| chr12:46809880
|
TG | T | 26 | a0001c0001t0001g0092a0001c0001t0001g0321a0001c0001t0001g0328others(23): Show | 30 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-304-6087delC | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46809880 | ||||||
| chr12:46810206
|
A | C | 1 | a0004c0004t0002g0201 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-304-6412T>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46810206 | ||||||
| chr12:46810262
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-304-6468C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46810262 | ||||||
| chr12:46810582
|
T | C | 26 | a0001c0001t0001g0092a0001c0001t0001g0321a0001c0001t0001g0328others(23): Show | 30 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-304-6788A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46810582 | ||||||
| chr12:46810589
|
T | C | 3 | a0002c0002t0002g0080a0002c0002t0002g0081a0002c0002t0002g0082 | 3 | HG00423.hp2 NA18992.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-304-6795A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46810589 | ||||||
| chr12:46810641
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-304-6847A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46810641 | ||||||
| chr12:46810692
|
G | A | 9 | a0001c0001t0001g0031a0001c0001t0001g0303a0001c0001t0001g0304others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-304-6898C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46810692 | ||||||
| chr12:46810726
|
A | T | 1 | a0001c0001t0003g0292 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-304-6932T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46810726 | ||||||
| chr12:46810901
|
A | G | 2 | a0001c0010t0001g0326a0003c0003t0002g0317 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-304-7107T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46810901 | ||||||
| chr12:46810993
|
A | G | 2 | a0001c0001t0006g0333a0001c0001t0019g0334 | 2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-304-7199T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46810993 | ||||||
| chr12:46811030
|
G | T | 26 | a0001c0001t0001g0092a0001c0001t0001g0321a0001c0001t0001g0328others(23): Show | 30 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-304-7236C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46811030 | ||||||
| chr12:46811471
|
C | G | 47 | a0001c0001t0005g0083a0001c0001t0005g0084a0002c0002t0001g0010others(44): Show | 61 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-304-7677G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46811471 | ||||||
| chr12:46811871
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0002g0301 | 3 | HG01167.hp2 HG01169.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-304-8077T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46811871 | ||||||
| chr12:46811875
|
C | CA | 56 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0255others(53): Show | 61 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.-304-8082dupT | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46811875 | ||||||
| chr12:46812029
|
A | G | 56 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0255others(53): Show | 61 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.-304-8235T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46812029 | ||||||
| chr12:46812439
|
A | G | 2 | a0002c0002t0001g0087a0002c0002t0002g0058 | 2 | HG01175.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-304-8645T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46812439 | ||||||
| chr12:46812485
|
G | A | 1 | a0001c0001t0003g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-304-8691C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46812485 | ||||||
| chr12:46812639
|
C | T | 4 | a0001c0001t0010g0169a0001c0001t0010g0171a0001c0001t0016g0172others(1): Show | 4 | HG02257.hp1 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-304-8845G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46812639 | ||||||
| chr12:46812932
|
T | C | 82 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0092others(79): Show | 91 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(88): Show |
intron_variant | MODIFIER | c.-304-9138A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46812932 | ||||||
| chr12:46813144
|
T | G | 1 | a0001c0001t0016g0172 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-304-9350A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46813144 | ||||||
| chr12:46813256
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-304-9462T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46813256 | ||||||
| chr12:46813270
|
G | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(85): Show | 101 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-304-9476C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46813270 | ||||||
| chr12:46813469
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0199a0001c0001t0001g0200 | 5 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(2): Show |
intron_variant | MODIFIER | c.-304-9675G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46813469 | ||||||
| chr12:46813477
|
A | G | 6 | a0001c0001t0010g0169a0001c0001t0010g0171a0001c0001t0016g0172others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-304-9683T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46813477 | ||||||
| chr12:46813491
|
G | A | 56 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0255others(53): Show | 61 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.-304-9697C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46813491 | ||||||
| chr12:46813556
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-304-9762A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46813556 | ||||||
| chr12:46813785
|
C | T | 1 | a0002c0002t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-304-9991G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46813785 | ||||||
| chr12:46813900
|
G | C | 1 | a0001c0001t0009g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-304-10106C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46813900 | ||||||
| chr12:46813940
|
T | C | 253 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(250): Show | 290 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.-304-10146A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46813940 | ||||||
| chr12:46813970
|
A | G | 26 | a0001c0001t0001g0092a0001c0001t0001g0321a0001c0001t0001g0328others(23): Show | 30 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-304-10176T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46813970 | ||||||
| chr12:46814035
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-304-10241A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814035 | ||||||
| chr12:46814042
|
A | G | 26 | a0001c0001t0001g0092a0001c0001t0001g0321a0001c0001t0001g0328others(23): Show | 30 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-304-10248T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814042 | ||||||
| chr12:46814085
|
T | C | 1 | a0003c0003t0002g0278 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-304-10291A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814085 | ||||||
| chr12:46814143
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-304-10349C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814143 | ||||||
| chr12:46814354
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-304-10560A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814354 | ||||||
| chr12:46814397
|
A | T | 1 | a0001c0001t0001g0091 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-304-10603T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814397 | ||||||
| chr12:46814506
|
T | C | 1 | a0001c0001t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-304-10712A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814506 | ||||||
| chr12:46814538
|
C | T | 1 | a0003c0003t0002g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-304-10744G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814538 | ||||||
| chr12:46814582
|
C | T | 253 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(250): Show | 290 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.-304-10788G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814582 | ||||||
| chr12:46814626
|
C | G | 1 | a0001c0001t0001g0017 | 2 | HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.-304-10832G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814626 | ||||||
| chr12:46814627
|
C | T | 1 | a0001c0001t0001g0017 | 2 | HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.-304-10833G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814627 | ||||||
| chr12:46814715
|
G | A | 56 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0255others(53): Show | 61 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.-304-10921C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814715 | ||||||
| chr12:46814858
|
A | G | 10 | a0001c0001t0001g0120a0001c0001t0001g0128a0001c0001t0001g0139others(7): Show | 10 | HG00733.hp2 HG01168.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-305+11045T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814858 | ||||||
| chr12:46814988
|
G | T | 56 | a0001c0001t0001g0088a0001c0001t0005g0083a0001c0001t0005g0084others(53): Show | 70 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-305+10915C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46814988 | ||||||
| chr12:46815020
|
A | T | 2 | a0001c0001t0005g0083a0001c0001t0005g0084 | 2 | NA18959.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-305+10883T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815020 | ||||||
| chr12:46815041
|
G | T | 1 | a0003c0003t0002g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-305+10862C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815041 | ||||||
| chr12:46815098
|
T | G | 1 | a0001c0001t0001g0226 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-305+10805A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815098 | ||||||
| chr12:46815240
|
G | GATATATA others(3): Show |
1 | a0001c0001t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-305+10653_-305+10 others(16): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815240 | ||||||
| chr12:46815240
|
GAT | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 42 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-305+10661_-305+10 others(8): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815240 | ||||||
| chr12:46815240
|
GATAT | G | 24 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(21): Show | 25 | HG01168.hp2 HG01433.hp1 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.-305+10659_-305+10 others(10): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815240 | ||||||
| chr12:46815240
|
GATATAT | G | 7 | a0001c0001t0001g0032a0001c0001t0001g0119a0001c0001t0001g0173others(4): Show | 8 | HG00673.hp1 HG02559.hp2 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.-305+10657_-305+10 others(12): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815240 | ||||||
| chr12:46815240
|
GATATATA others(1): Show |
G | 29 | a0001c0001t0001g0029a0001c0001t0001g0161a0001c0001t0001g0256others(26): Show | 33 | HG00408.hp2 HG01192.hp2 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.-305+10655_-305+10 others(14): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815240 | ||||||
| chr12:46815240
|
GATATATA others(3): Show |
G | 9 | a0001c0001t0001g0262a0001c0001t0001g0304a0001c0001t0001g0321others(6): Show | 9 | HG01884.hp1 HG02129.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.-305+10653_-305+10 others(16): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815240 | ||||||
| chr12:46815240
|
GATATATA others(5): Show |
G | 25 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0328others(22): Show | 28 | HG00621.hp1 HG01261.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.-305+10651_-305+10 others(18): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815240 | ||||||
| chr12:46815240
|
GATATATA others(7): Show |
G | 25 | a0001c0001t0001g0030a0001c0001t0001g0175a0001c0001t0001g0176others(22): Show | 27 | HG00597.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-305+10649_-305+10 others(20): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815240 | ||||||
| chr12:46815240
|
GATATATA others(9): Show |
G | 66 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(63): Show | 78 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-305+10647_-305+10 others(22): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815240 | ||||||
| chr12:46815240
|
GATATATA others(11): Show |
G | 6 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0227others(3): Show | 6 | HG01255.hp2 HG02083.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-305+10645_-305+10 others(24): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815240 | ||||||
| chr12:46815240
|
GATATATA others(19): Show |
G | 2 | a0001c0001t0001g0092a0011c0017t0002g0168 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-305+10637_-305+10 others(32): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815240 | ||||||
| chr12:46815240
|
GATATATA others(21): Show |
G | 1 | a0001c0005t0001g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-305+10635_-305+10 others(34): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815240 | ||||||
| chr12:46815264
|
TATATATA others(17): Show |
T | 49 | a0001c0001t0001g0088a0001c0001t0005g0083a0001c0001t0005g0084others(46): Show | 63 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-305+10615_-305+10 others(30): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815264 | ||||||
| chr12:46815266
|
TATATATA others(15): Show |
T | 2 | a0002c0002t0001g0055a0002c0002t0002g0056 | 2 | HG02132.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.-305+10615_-305+10 others(28): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815266 | ||||||
| chr12:46815266
|
TATATATA others(17): Show |
T | 2 | a0002c0002t0001g0053a0002c0002t0001g0054 | 2 | NA18949.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-305+10613_-305+10 others(30): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815266 | ||||||
| chr12:46815268
|
TATATATA others(13): Show |
T | 1 | a0001c0001t0019g0334 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-305+10615_-305+10 others(26): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815268 | ||||||
| chr12:46815268
|
TATATATA others(15): Show |
T | 1 | a0001c0005t0015g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-305+10613_-305+10 others(28): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815268 | ||||||
| chr12:46815270
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0006g0333 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-305+10615_-305+10 others(24): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815270 | ||||||
| chr12:46815274
|
T | C | 2 | a0001c0001t0002g0271a0003c0003t0002g0283 | 2 | HG02080.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-305+10629A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815274 | ||||||
| chr12:46815276
|
T | C | 18 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0265others(15): Show | 19 | HG01884.hp2 HG02080.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.-305+10627A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815276 | ||||||
| chr12:46815278
|
T | C | 45 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(42): Show | 49 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-305+10625A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815278 | ||||||
| chr12:46815278
|
TATATATA others(1): Show |
T | 5 | a0001c0001t0001g0031a0001c0001t0001g0307a0001c0001t0002g0301others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-305+10617_-305+10 others(14): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815278 | ||||||
| chr12:46815278
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0005g0036a0001c0001t0005g0037 | 2 | HG01516.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-305+10615_-305+10 others(16): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815278 | ||||||
| chr12:46815280
|
T | C | 56 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0164others(53): Show | 61 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.-305+10623A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815280 | ||||||
| chr12:46815282
|
T | C | 65 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0163others(62): Show | 70 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(67): Show |
intron_variant | MODIFIER | c.-305+10621A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815282 | ||||||
| chr12:46815282
|
TATACAC | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0089a0001c0001t0005g0043 | 3 | HG01099.hp2 NA18522.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-305+10615_-305+10 others(12): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815282 | ||||||
| chr12:46815284
|
T | C | 219 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(216): Show | 246 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.-305+10619A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815284 | ||||||
| chr12:46815284
|
T | TAC | 7 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG03540.hp1 NA18974.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.-305+10617_-305+10 others(8): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815284 | ||||||
| chr12:46815284
|
T | TATATAC | 3 | a0001c0001t0001g0091a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG03490.hp2 HG04199.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.-305+10618_-305+10 others(12): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815284 | ||||||
| chr12:46815284
|
TACAC | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0005g0040 | 3 | HG01975.hp2 NA18948.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-305+10615_-305+10 others(10): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815284 | ||||||
| chr12:46815288
|
C | T | 1 | a0001c0001t0005g0044 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-305+10615G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815288 | ||||||
| chr12:46815308
|
C | G | 4 | a0001c0001t0010g0169a0001c0001t0010g0171a0001c0001t0016g0172others(1): Show | 4 | HG02257.hp1 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-305+10595G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815308 | ||||||
| chr12:46815310
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-305+10593C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815310 | ||||||
| chr12:46815512
|
A | G | 1 | a0003c0003t0002g0283 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-305+10391T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815512 | ||||||
| chr12:46815531
|
T | C | 339 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(336): Show | 383 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(380): Show |
intron_variant | MODIFIER | c.-305+10372A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815531 | ||||||
| chr12:46815548
|
T | A | 1 | a0001c0001t0001g0239 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-305+10355A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815548 | ||||||
| chr12:46815584
|
G | T | 1 | a0001c0001t0002g0258 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-305+10319C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815584 | ||||||
| chr12:46815675
|
A | T | 1 | a0002c0002t0002g0051 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-305+10228T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815675 | ||||||
| chr12:46815686
|
C | T | 40 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(37): Show | 44 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(41): Show |
intron_variant | MODIFIER | c.-305+10217G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815686 | ||||||
| chr12:46815876
|
T | G | 1 | a0003c0003t0002g0272 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-305+10027A>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815876 | ||||||
| chr12:46816334
|
A | G | 14 | a0001c0001t0001g0030a0001c0001t0001g0294a0001c0001t0002g0271others(11): Show | 15 | HG01192.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-305+9569T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46816334 | ||||||
| chr12:46816759
|
C | T | 4 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | HG00280.hp2 HG01257.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-305+9144G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46816759 | ||||||
| chr12:46817047
|
T | TA | 74 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(71): Show | 88 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-305+8855dupT | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46817047 | ||||||
| chr12:46817254
|
C | T | 56 | a0001c0001t0001g0088a0001c0001t0005g0083a0001c0001t0005g0084others(53): Show | 70 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-305+8649G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46817254 | ||||||
| chr12:46817283
|
A | G | 82 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0092others(79): Show | 91 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(88): Show |
intron_variant | MODIFIER | c.-305+8620T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46817283 | ||||||
| chr12:46817292
|
T | C | 2 | a0001c0001t0005g0083a0001c0001t0005g0084 | 2 | NA18959.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-305+8611A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46817292 | ||||||
| chr12:46817330
|
T | C | 1 | a0001c0001t0003g0297 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-305+8573A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46817330 | ||||||
| chr12:46817396
|
C | CT | 253 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(250): Show | 290 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.-305+8506dupA | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46817396 | ||||||
| chr12:46817516
|
C | T | 1 | a0001c0001t0009g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-305+8387G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46817516 | ||||||
| chr12:46817522
|
C | T | 6 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 6 | HG01167.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-305+8381G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46817522 | ||||||
| chr12:46817901
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-305+8002T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46817901 | ||||||
| chr12:46817925
|
T | C | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231 | 3 | HG00423.hp1 NA19070.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-305+7978A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46817925 | ||||||
| chr12:46818162
|
T | A | 21 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0003g0318others(18): Show | 24 | HG02074.hp1 HG02523.hp1 NA18939.hp2 others(21): Show |
intron_variant | MODIFIER | c.-305+7741A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46818162 | ||||||
| chr12:46818303
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0005g0187 | 2 | NA18961.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-305+7600G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46818303 | ||||||
| chr12:46818308
|
A | G | 1 | a0001c0001t0010g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-305+7595T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46818308 | ||||||
| chr12:46818587
|
A | G | 101 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(98): Show | 115 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-305+7316T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46818587 | ||||||
| chr12:46818896
|
C | A | 1 | a0003c0003t0002g0268 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-305+7007G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46818896 | ||||||
| chr12:46818999
|
A | T | 1 | a0001c0001t0002g0295 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-305+6904T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46818999 | ||||||
| chr12:46819019
|
G | T | 8 | a0001c0001t0001g0088a0001c0001t0006g0333a0001c0001t0006g0335others(5): Show | 8 | HG02055.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-305+6884C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46819019 | ||||||
| chr12:46819025
|
T | TA | 25 | a0001c0001t0001g0321a0001c0001t0001g0328a0001c0001t0001g0329others(22): Show | 29 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-305+6877dupT | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46819025 | ||||||
| chr12:46819133
|
G | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(141): Show | 162 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-305+6770C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46819133 | ||||||
| chr12:46819162
|
C | T | 1 | a0001c0001t0004g0330 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-305+6741G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46819162 | ||||||
| chr12:46819386
|
A | G | 9 | a0001c0001t0001g0031a0001c0001t0001g0303a0001c0001t0001g0304others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-305+6517T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46819386 | ||||||
| chr12:46819429
|
G | A | 4 | a0001c0001t0010g0169a0001c0001t0010g0171a0001c0001t0016g0172others(1): Show | 4 | HG02257.hp1 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-305+6474C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46819429 | ||||||
| chr12:46819463
|
A | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG01167.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-305+6440T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46819463 | ||||||
| chr12:46819494
|
G | T | 1 | a0001c0001t0008g0279 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-305+6409C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46819494 | ||||||
| chr12:46819602
|
C | T | 10 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(7): Show | 10 | NA18948.hp2 NA18962.hp1 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-305+6301G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46819602 | ||||||
| chr12:46819637
|
G | A | 4 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG01081.hp1 HG01261.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-305+6266C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46819637 | ||||||
| chr12:46820085
|
A | T | 253 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(250): Show | 290 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.-305+5818T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820085 | ||||||
| chr12:46820184
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-305+5719A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820184 | ||||||
| chr12:46820346
|
C | T | 60 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(57): Show | 74 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.-305+5557G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820346 | ||||||
| chr12:46820438
|
T | C | 145 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(142): Show | 163 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.-305+5465A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820438 | ||||||
| chr12:46820509
|
T | C | 170 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(167): Show | 192 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.-305+5394A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820509 | ||||||
| chr12:46820590
|
G | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(141): Show | 162 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-305+5313C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820590 | ||||||
| chr12:46820623
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0003g0093 | 2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-305+5280G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820623 | ||||||
| chr12:46820690
|
C | A | 1 | a0001c0001t0001g0236 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-305+5213G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820690 | ||||||
| chr12:46820733
|
C | A | 253 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(250): Show | 290 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.-305+5170G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820733 | ||||||
| chr12:46820787
|
C | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(141): Show | 162 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-305+5116G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820787 | ||||||
| chr12:46820866
|
C | T | 6 | a0001c0001t0010g0169a0001c0001t0010g0171a0001c0001t0016g0172others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-305+5037G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820866 | ||||||
| chr12:46820894
|
A | G | 4 | a0002c0002t0002g0001a0002c0002t0002g0048a0002c0002t0002g0049others(1): Show | 8 | NA18939.hp1 NA18967.hp2 NA18981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-305+5009T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820894 | ||||||
| chr12:46820895
|
T | C | 2 | a0002c0002t0002g0085a0002c0002t0002g0086 | 2 | HG02015.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.-305+5008A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820895 | ||||||
| chr12:46820914
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-305+4989C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820914 | ||||||
| chr12:46821071
|
A | G | 25 | a0001c0001t0001g0321a0001c0001t0001g0328a0001c0001t0001g0329others(22): Show | 29 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-305+4832T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821071 | ||||||
| chr12:46821110
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-305+4793A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821110 | ||||||
| chr12:46821248
|
A | G | 12 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(9): Show | 12 | HG01099.hp2 HG01361.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.-305+4655T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821248 | ||||||
| chr12:46821282
|
T | C | 1 | a0002c0002t0002g0165 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-305+4621A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821282 | ||||||
| chr12:46821443
|
G | A | 1 | a0001c0001t0004g0332 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-305+4460C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821443 | ||||||
| chr12:46821465
|
G | A | 9 | a0001c0001t0001g0031a0001c0001t0001g0303a0001c0001t0001g0304others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-305+4438C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821465 | ||||||
| chr12:46821473
|
T | A | 1 | a0001c0001t0001g0166 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-305+4430A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821473 | ||||||
| chr12:46821554
|
G | C | 6 | a0001c0001t0010g0169a0001c0001t0010g0171a0001c0001t0016g0172others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-305+4349C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821554 | ||||||
| chr12:46821576
|
A | G | 1 | a0001c0001t0001g0015 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.-305+4327T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821576 | ||||||
| chr12:46821637
|
A | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-305+4266T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821637 | ||||||
| chr12:46821701
|
A | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0294 | 3 | HG02630.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-305+4202T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821701 | ||||||
| chr12:46821759
|
C | T | 1 | a0001c0001t0005g0174 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-305+4144G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821759 | ||||||
| chr12:46821890
|
C | T | 1 | a0002c0002t0002g0038 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-305+4013G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821890 | ||||||
| chr12:46821919
|
C | A | 1 | a0002c0002t0001g0087 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-305+3984G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821919 | ||||||
| chr12:46821965
|
C | T | 2 | a0001c0001t0005g0036a0001c0001t0005g0037 | 2 | HG01516.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-305+3938G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46821965 | ||||||
| chr12:46822230
|
G | T | 1 | a0001c0001t0001g0246 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-305+3673C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46822230 | ||||||
| chr12:46822232
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-305+3671A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46822232 | ||||||
| chr12:46822406
|
T | C | 25 | a0001c0001t0001g0321a0001c0001t0001g0328a0001c0001t0001g0329others(22): Show | 29 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-305+3497A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46822406 | ||||||
| chr12:46822446
|
G | C | 1 | a0001c0001t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-305+3457C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46822446 | ||||||
| chr12:46822714
|
G | C | 170 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(167): Show | 192 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.-305+3189C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46822714 | ||||||
| chr12:46822864
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-305+3039A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46822864 | ||||||
| chr12:46822872
|
A | T | 1 | a0003c0003t0002g0317 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-305+3031T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46822872 | ||||||
| chr12:46823005
|
T | C | 1 | a0001c0001t0002g0306 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-305+2898A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46823005 | ||||||
| chr12:46823198
|
G | A | 2 | a0001c0001t0005g0237a0001c0001t0005g0238 | 2 | HG02083.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-305+2705C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46823198 | ||||||
| chr12:46823273
|
G | A | 170 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(167): Show | 192 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.-305+2630C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46823273 | ||||||
| chr12:46823295
|
A | G | 1 | a0001c0001t0003g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-305+2608T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46823295 | ||||||
| chr12:46823444
|
G | C | 1 | a0001c0001t0001g0239 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-305+2459C>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46823444 | ||||||
| chr12:46823731
|
G | A | 144 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(141): Show | 162 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-305+2172C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46823731 | ||||||
| chr12:46823845
|
C | T | 43 | a0001c0001t0001g0029a0001c0001t0001g0255a0001c0001t0001g0256others(40): Show | 47 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.-305+2058G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46823845 | ||||||
| chr12:46824068
|
G | A | 8 | a0001c0001t0001g0088a0001c0001t0006g0333a0001c0001t0006g0335others(5): Show | 8 | HG02055.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-305+1835C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46824068 | ||||||
| chr12:46824157
|
A | T | 170 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(167): Show | 192 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.-305+1746T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46824157 | ||||||
| chr12:46824361
|
G | T | 170 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(167): Show | 192 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.-305+1542C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46824361 | ||||||
| chr12:46824697
|
A | T | 1 | a0001c0001t0001g0091 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-305+1206T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46824697 | ||||||
| chr12:46824698
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-305+1205C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46824698 | ||||||
| chr12:46824719
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-305+1184T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46824719 | ||||||
| chr12:46824994
|
C | T | 68 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(65): Show | 82 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.-305+909G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46824994 | ||||||
| chr12:46825015
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-305+888A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825015 | ||||||
| chr12:46825095
|
ACTGGAGG others(129): Show |
A | 18 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0265others(15): Show | 20 | HG00408.hp2 HG00673.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.-305+672_-305+807d others(2): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825095 | ||||||
| chr12:46825313
|
T | TATATATA others(22): Show |
1 | a0001c0001t0004g0330 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-305+589_-305+590i others(31): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TATATATA others(26): Show |
1 | a0001c0001t0003g0299 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-305+589_-305+590i others(35): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATA | 80 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(77): Show | 93 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.-305+584_-305+589d others(8): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(1): Show |
5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02080.hp2 HG02735.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.-305+582_-305+589d others(10): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(3): Show |
26 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(23): Show | 29 | HG00408.hp2 HG01192.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.-305+580_-305+589d others(12): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(5): Show |
19 | a0001c0001t0001g0029a0001c0001t0001g0275a0001c0001t0002g0035others(16): Show | 20 | HG00673.hp1 HG02080.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-305+578_-305+589d others(14): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(9): Show |
2 | a0003c0003t0002g0287a0006c0018t0002g0288 | 2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-305+574_-305+589d others(18): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(11): Show |
1 | a0003c0003t0002g0289 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-305+589_-305+590i others(20): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0002g0290 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-305+589_-305+590i others(22): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(15): Show |
3 | a0001c0001t0001g0030a0001c0001t0004g0316a0002c0002t0014g0315 | 4 | HG02809.hp2 HG03041.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.-305+589_-305+590i others(24): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(17): Show |
10 | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0001t0003g0318others(7): Show | 12 | HG02074.hp1 HG02895.hp1 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.-305+589_-305+590i others(26): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(19): Show |
2 | a0001c0001t0004g0320a0010c0015t0003g0293 | 2 | HG02258.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-305+589_-305+590i others(28): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(21): Show |
8 | a0001c0001t0001g0294a0001c0001t0001g0321a0001c0001t0002g0295others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-305+589_-305+590i others(30): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(23): Show |
7 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0003g0297others(4): Show | 8 | HG01884.hp1 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-305+589_-305+590i others(32): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(25): Show |
2 | a0001c0001t0004g0034a0001c0001t0004g0331 | 3 | HG01257.hp1 HG01258.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-305+589_-305+590i others(34): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(27): Show |
1 | a0001c0001t0003g0298 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-305+589_-305+590i others(36): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825313
|
T | TTATATAT others(29): Show |
1 | a0001c0001t0004g0332 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-305+589_-305+590i others(38): Show |
SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825313 | ||||||
| chr12:46825330
|
T | A | 1 | a0001c0001t0001g0307 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-305+573A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825330 | ||||||
| chr12:46825538
|
G | A | 4 | a0001c0001t0004g0311a0001c0001t0004g0312a0001c0001t0004g0313others(1): Show | 4 | NA18961.hp2 NA18988.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.-305+365C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825538 | ||||||
| chr12:46825539
|
G | T | 4 | a0001c0001t0004g0311a0001c0001t0004g0312a0001c0001t0004g0313others(1): Show | 4 | NA18961.hp2 NA18988.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.-305+364C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825539 | ||||||
| chr12:46825580
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-305+323T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825580 | ||||||
| chr12:46825617
|
G | A | 9 | a0001c0001t0001g0031a0001c0001t0001g0303a0001c0001t0001g0304others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-305+286C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825617 | ||||||
| chr12:46825653
|
T | A | 25 | a0001c0001t0001g0321a0001c0001t0001g0328a0001c0001t0001g0329others(22): Show | 29 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-305+250A>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825653 | ||||||
| chr12:46825653
|
T | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0308a0001c0001t0001g0309others(1): Show | 5 | HG02559.hp2 HG06807.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.-305+250A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46825653 |