Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MDPME others(542): Show |
chr12 | 46759761 | 46830997 |
| a0002 | 0/0 | 547 | 54 | 1 | 4 | 43 | 1 | 5 | 31 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(542): Show |
chr12 | 46759761 | 46830997 |
| a0003 | 0/0 | 547 | 42 | 24 | 1 | 16 | 0 | 1 | 13 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(542): Show |
chr12 | 46759761 | 46830997 |
| a0004 | 0/0 | 547 | 11 | 0 | 10 | 1 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(542): Show |
chr12 | 46759761 | 46830997 |
| a0005 | 0/0 | 241 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(236): Show |
chr12 | 46759761 | 46830997 |
| a0006 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(542): Show |
chr12 | 46759761 | 46830997 |
| a0007 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(542): Show |
chr12 | 46759761 | 46830997 |
| a0008 | 0/0 | 547 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(542): Show |
chr12 | 46759761 | 46830997 |
| a0009 | 0/0 | 547 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(542): Show |
chr12 | 46759761 | 46830997 |
| a0010 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(542): Show |
chr12 | 46759761 | 46830997 |
| a0011 | 0/0 | 231 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(226): Show |
chr12 | 46759761 | 46830997 |
| a0012 | 0/0 | 547 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(542): Show |
chr12 | 46759761 | 46830997 |
| a0013 | 0/0 | 547 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(542): Show |
chr12 | 46759761 | 46830997 |
| a0014 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | MDPME others(542): Show |
chr12 | 46759761 | 46830997 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1641 | 260 | 61 | 45 | 119 | 9 | 24 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0001c0005 | 0/0 | 1641 | 3 | 3 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0001c0008 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0001c0010 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0001c0016 | 0/0 | 1641 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0002c0002 | 0/0 | 1641 | 54 | 1 | 4 | 43 | 1 | 5 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0003c0003 | 0/0 | 1641 | 42 | 24 | 1 | 16 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0004c0004 | 0/0 | 1641 | 11 | 0 | 10 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0005c0006 | 0/0 | 1641 | 2 | 0 | 0 | 0 | 0 | 2 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0006c0017 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0007c0015 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0008c0014 | 0/0 | 1641 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0009c0012 | 0/0 | 1641 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0010c0018 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0011c0009 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0012c0011 | 0/0 | 1641 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0013c0007 | 0/0 | 1641 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
chr12 | 46759761 | 46830997 | ||
| a0014c0013 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ATGGA others(1636): Show |
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 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0002 | 0/0 | 3983 | 9 | 7 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0003 | 0/0 | 3983 | 21 | 8 | 1 | 9 | 0 | 3 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0004 | 0/0 | 3983 | 23 | 0 | 2 | 21 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0005 | 0/0 | 3983 | 19 | 0 | 1 | 9 | 3 | 6 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0006 | 0/0 | 3983 | 6 | 6 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0007 | 0/0 | 3983 | 3 | 0 | 2 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0008 | 0/0 | 3983 | 3 | 3 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0009 | 1/0 | 3983 | 2 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0010 | 0/0 | 3983 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0016 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0017 | 0/0 | 3983 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0018 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0019 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0001t0020 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0005t0001 | 0/0 | 3983 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0005t0015 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0008t0001 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0010t0001 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0001c0016t0001 | 0/0 | 3983 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0002c0002t0001 | 0/0 | 3983 | 11 | 0 | 2 | 5 | 1 | 3 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0002c0002t0002 | 0/0 | 3983 | 38 | 1 | 0 | 37 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0002c0002t0003 | 0/0 | 3983 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0002c0002t0005 | 0/0 | 3983 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0002c0002t0012 | 0/0 | 3983 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0002c0002t0013 | 0/0 | 3983 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0002c0002t0014 | 0/0 | 3983 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0003c0003t0002 | 0/0 | 3983 | 42 | 24 | 1 | 16 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0004c0004t0002 | 0/0 | 3983 | 11 | 0 | 10 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0005c0006t0001 | 0/0 | 3983 | 2 | 0 | 0 | 0 | 0 | 2 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0006c0017t0002 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0007c0015t0003 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0008c0014t0001 | 0/0 | 3983 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0009c0012t0001 | 0/0 | 3983 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0010c0018t0002 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0011c0009t0002 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0012c0011t0002 | 0/0 | 3983 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0013c0007t0011 | 0/0 | 3983 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| a0014c0013t0001 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | ACTGG others(3978): Show |
chr12 | 46759761 | 46830997 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 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 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 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 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0093 | 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 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0112 | 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 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0238 | 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 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0301 | 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 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0306 | 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 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0003g0295 | 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 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0310 | 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 |
| a0001c0001t0004g0313 | 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 |
| a0001c0001t0004g0317 | 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 |
| a0001c0001t0004g0321 | 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 |
| a0001c0001t0004g0324 | 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 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0042 | 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 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0006g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0006g0332 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0006g0334 | 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 |
| a0001c0001t0007g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0008g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0009g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0016g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0017g0193 | 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 |
| a0001c0001t0019g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0001t0020g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0005t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0005t0015g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0008t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0010t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0001c0016t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0001g0086 | 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 |
| a0002c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 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 |
| a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0047 | 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 |
| a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0054 | 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 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0058 | 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 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0074 | 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 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0084 | 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 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0012g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0013g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0002c0002t0014g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0248 | 0/0 | 1 | 1 | 0 | 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 |
| a0003c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0003c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0003c0003t0002g0271 | 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 |
| a0003c0003t0002g0275 | 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 |
| a0003c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0003c0003t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0004c0004t0002g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0004c0004t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0004c0004t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0004c0004t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0004c0004t0002g0063 | 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 |
| a0004c0004t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0005c0006t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0005c0006t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0006c0017t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0007c0015t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0008c0014t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0009c0012t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0010c0018t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0011c0009t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0012c0011t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0013c0007t0011g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| a0014c0013t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0070 | EUR | FIN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00642 | hp1 | a0002 | c0002 | t0013 | g0115 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00673 | hp1 | a0003 | c0003 | t0002 | g0282 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | CHS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01071 | hp2 | a0004 | c0004 | t0002 | g0003 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0140 | 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 | g0055 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0013 | 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 | g0032 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01175 | hp1 | a0002 | c0002 | t0003 | g0061 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01192 | hp2 | a0003 | c0003 | t0002 | g0244 | AMR | PUR | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0224 | 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 | g0024 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0023 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0023 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01496 | hp2 | a0004 | c0004 | t0002 | g0003 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0028 | EUR | IBS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0038 | EUR | IBS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0028 | EUR | IBS | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01884 | hp1 | a0001 | c0010 | t0001 | g0323 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01884 | hp2 | a0003 | c0003 | t0002 | g0286 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0298 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01928 | hp2 | a0004 | c0004 | t0002 | g0063 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01975 | hp1 | a0004 | c0004 | t0002 | g0003 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01981 | hp1 | a0004 | c0004 | t0002 | g0062 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01993 | hp2 | a0004 | c0004 | t0002 | g0011 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02055 | hp1 | a0003 | c0003 | t0002 | g0284 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0330 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0316 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02080 | hp1 | a0003 | c0003 | t0002 | g0280 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0235 | 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 | g0156 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0334 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02145 | hp2 | a0006 | c0017 | t0002 | g0164 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02148 | hp1 | a0004 | c0004 | t0002 | g0011 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02155 | hp2 | a0003 | c0003 | t0002 | g0113 | EAS | CDX | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02257 | hp1 | a0001 | c0001 | t0016 | g0169 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02258 | hp1 | a0001 | c0005 | t0015 | g0081 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02258 | hp2 | a0007 | c0015 | t0003 | g0290 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02273 | hp2 | a0004 | c0004 | t0002 | g0003 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02280 | hp1 | a0003 | c0003 | t0002 | g0249 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02300 | hp1 | a0004 | c0004 | t0002 | g0064 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02451 | hp2 | a0003 | c0003 | t0002 | g0268 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0328 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02572 | hp2 | a0003 | c0003 | t0002 | g0247 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0051 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02602 | hp2 | a0008 | c0014 | t0001 | g0221 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02615 | hp1 | a0003 | c0003 | t0002 | g0278 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0332 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0296 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0302 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02683 | hp1 | a0001 | c0001 | t0007 | g0212 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02683 | hp2 | a0009 | c0012 | t0001 | g0119 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0066 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0041 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02717 | hp1 | a0003 | c0003 | t0002 | g0248 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0331 | 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 | g0293 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0099 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02818 | hp1 | a0001 | c0008 | t0001 | g0096 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02818 | hp2 | a0010 | c0018 | t0002 | g0285 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02886 | hp1 | a0003 | c0003 | t0002 | g0125 | 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 | g0288 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02896 | hp2 | a0003 | c0003 | t0002 | g0027 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02897 | hp2 | a0003 | c0003 | t0002 | g0027 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02965 | hp2 | a0003 | c0003 | t0002 | g0269 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02970 | hp1 | a0001 | c0001 | t0020 | g0337 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02970 | hp2 | a0003 | c0003 | t0002 | g0250 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0277 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03098 | hp1 | a0003 | c0003 | t0002 | g0253 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0333 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0276 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03139 | hp1 | a0003 | c0003 | t0002 | g0167 | 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 | g0304 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03195 | hp2 | a0011 | c0009 | t0002 | g0245 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03209 | hp2 | a0003 | c0003 | t0002 | g0271 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0168 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03453 | hp1 | a0003 | c0003 | t0002 | g0273 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0297 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03486 | hp2 | a0003 | c0003 | t0002 | g0275 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0126 | 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 | g0072 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03492 | hp2 | a0005 | c0006 | t0001 | g0071 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03516 | hp2 | a0003 | c0003 | t0002 | g0206 | AFR | ESN | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03540 | hp1 | a0003 | c0003 | t0002 | g0124 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0052 | AFR | GWD | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0165 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03579 | hp2 | a0003 | c0003 | t0002 | g0270 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03688 | hp2 | a0003 | c0003 | t0002 | g0283 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0037 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0186 | SAS | PJL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0234 | SAS | BEB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0129 | SAS | BEB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04184 | hp1 | a0002 | c0002 | t0012 | g0068 | SAS | BEB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | BEB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0215 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG04228 | hp2 | a0002 | c0002 | t0005 | g0065 | SAS | STU | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | CHB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | CHB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0166 | AFR | YRI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18906 | hp2 | a0003 | c0003 | t0002 | g0314 | AFR | YRI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0130 | 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 | g0050 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18945 | hp1 | a0003 | c0003 | t0002 | g0260 | 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 | g0240 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18947 | hp1 | a0004 | c0004 | t0002 | g0199 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0171 | 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 | g0222 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18953 | hp1 | a0003 | c0003 | t0002 | g0219 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0082 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18962 | hp2 | a0012 | c0011 | t0002 | g0264 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18967 | hp1 | a0001 | c0001 | t0017 | g0193 | 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 | g0026 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18969 | hp2 | a0003 | c0003 | t0002 | g0259 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0021 | 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 | g0114 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18978 | hp2 | a0003 | c0003 | t0002 | g0281 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0012 | 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 | g0317 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18984 | hp2 | a0002 | c0002 | t0014 | g0312 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0308 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18989 | hp1 | a0003 | c0003 | t0002 | g0205 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18989 | hp2 | a0003 | c0003 | t0002 | g0265 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18998 | hp1 | a0013 | c0007 | t0011 | g0059 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA18999 | hp2 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19000 | hp2 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0146 | 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 | g0005 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19009 | hp2 | a0003 | c0003 | t0002 | g0029 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0121 | 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 | g0315 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0208 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | LWK | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | LWK | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0279 | AFR | LWK | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | LWK | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0220 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19060 | hp2 | a0003 | c0003 | t0002 | g0029 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19062 | hp1 | a0003 | c0003 | t0002 | g0257 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19075 | hp1 | a0001 | c0001 | t0005 | g0209 | 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 | g0204 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0195 | 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 | g0007 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19091 | hp1 | a0001 | c0016 | t0001 | g0137 | 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 | g0123 | AFR | YRI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA19240 | hp2 | a0001 | c0001 | t0019 | g0336 | AFR | YRI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ASW | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20129 | hp2 | a0003 | c0003 | t0002 | g0246 | AFR | ASW | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | TSI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | GIH | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0042 | SAS | GIH | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02109 | hp1 | a0003 | c0003 | t0002 | g0274 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0335 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0295 | AFR | MSL | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | USA | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20300 | hp1 | a0014 | c0013 | t0001 | g0190 | AFR | USA | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | USA | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0225 | REF | REF | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0009 | g0116 | REF | REF | SLC38A4_chr12_46759761_46830997 | SLC38A4 | chr12 | 46759761 | 46830997 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:46768312 | C | T | 1 | a0006 | 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 | a0007 | 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 | a0008 | 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 | a0003 a0004 a0010 others(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 | a0014 | 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 | a0013 | 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 | a0009 | 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 | a0012 | 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 | a0011 | 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 | a0002 a0004 a0005 others(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 | a0010 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0005 a0006c0017 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0002c0002t0012 a0002c0002t0013 |
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 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0020 others(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 | a0001c0001t0005 a0002c0002t0005 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(35): Show |
381 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(378): 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 | a0001c0001t0004 a0001c0001t0010 |
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 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(15): Show |
204 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(201): 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 | a0013c0007t0011 | 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 | a0001c0001t0006 a0001c0001t0019 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:46767238 | A | ATG | 9 | a0001c0001t0002g0036 a0001c0001t0002g0128 a0001c0001t0002g0298 others(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 | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0005g0028 a0001c0001t0005g0037 a0001c0001t0005g0038 others(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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0262 a0001c0001t0001g0266 |
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 | a0002c0002t0013g0115 | 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 | a0001c0001t0005g0186 | 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 | a0001c0001t0001g0213 a0001c0001t0001g0241 |
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 | a0001c0001t0005g0184 | 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 | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(176): Show |
204 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1542+118C>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 16/16 | chr12 | 46768192 | |||||||
| chr12:46768428 | C | T | 62 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(59): Show |
70 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(67): 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 | a0001c0001t0005g0184 | 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 | a0001c0001t0001g0160 a0001c0001t0001g0236 |
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 | a0002c0002t0001g0077 | 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 | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(176): Show |
204 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1444+178T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 15/16 | chr12 | 46769106 | |||||||
| chr12:46769155 | T | G | 334 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(331): Show |
381 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(378): 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 | a0001c0001t0002g0287 a0001c0001t0002g0299 a0001c0001t0002g0303 others(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 | a0001c0001t0008g0276 a0001c0001t0008g0277 a0001c0001t0008g0279 |
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 | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(176): Show |
204 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(201): 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 | a0001c0001t0003g0017 a0001c0001t0003g0092 a0001c0001t0003g0132 others(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 | 270 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
304 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(301): 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 | a0001c0001t0007g0023 a0001c0001t0007g0212 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0091 a0001c0001t0001g0301 |
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 | 179 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(176): Show |
204 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1300-907C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46770335 | |||||||
| chr12:46770529 | T | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0135 others(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 | a0001c0001t0002g0267 a0001c0001t0002g0292 a0001c0001t0019g0336 |
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 | 334 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(331): Show |
381 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(378): 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 | a0001c0001t0002g0292 a0001c0001t0019g0336 |
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 | 187 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
212 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1300-1957T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46771385 | |||||||
| chr12:46771540 | C | G | 187 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
212 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1300-2112G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46771540 | |||||||
| chr12:46771646 | T | C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): 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 | a0001c0001t0002g0128 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0272 |
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 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0299 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0088 a0001c0001t0002g0255 a0001c0001t0004g0007 others(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 | 110 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): 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 | 110 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): 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 | a0001c0001t0001g0100 | 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 | a0003c0003t0002g0019 a0003c0003t0002g0027 a0003c0003t0002g0029 others(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 | a0001c0001t0005g0042 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0138 a0001c0001t0001g0291 others(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 | 174 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(195): 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 | a0001c0001t0001g0210 | 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 | 334 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(331): Show |
381 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(378): Show |
intron_variant | MODIFIER | c.1299+1796T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46773253 | |||||||
| chr12:46773291 | C | T | 55 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(52): Show |
62 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1299+1758G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 14/16 | chr12 | 46773291 | |||||||
| chr12:46773295 | G | A | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
189 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(186): 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 | a0003c0003t0002g0029 a0003c0003t0002g0259 a0003c0003t0002g0263 others(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 | a0001c0001t0002g0128 | 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 | a0001c0001t0002g0267 a0001c0001t0002g0292 a0001c0001t0019g0336 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0138 a0001c0001t0001g0291 others(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 | a0001c0001t0002g0255 a0002c0002t0001g0078 a0002c0002t0002g0001 others(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 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0299 others(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 | 334 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(331): Show |
381 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(378): 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 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0272 |
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 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(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 | a0003c0003t0002g0273 a0010c0018t0002g0285 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0091 a0001c0001t0001g0301 |
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 | 13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0108 others(10): 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 | a0001c0001t0002g0267 a0001c0001t0002g0292 a0001c0001t0019g0336 |
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 | a0001c0001t0002g0255 a0002c0002t0001g0078 a0002c0002t0002g0001 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0138 a0001c0001t0001g0291 others(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 | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): 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 | a0001c0001t0001g0031 a0001c0001t0001g0291 a0001c0001t0003g0288 others(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 | a0002c0002t0012g0068 a0002c0002t0013g0115 |
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 | a0001c0001t0002g0287 a0001c0001t0002g0298 a0001c0001t0002g0299 others(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 | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
218 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(215): 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 | a0001c0010t0001g0323 | 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 | a0001c0001t0001g0148 | 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 | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): 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 | a0002c0002t0013g0115 | 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 | a0003c0003t0002g0273 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0091 a0001c0001t0001g0301 |
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 | a0001c0001t0004g0311 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0091 a0001c0001t0001g0301 |
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 | a0001c0001t0002g0267 a0001c0001t0002g0292 a0001c0001t0019g0336 |
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 | 334 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(331): Show |
381 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(378): 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 | a0001c0005t0001g0165 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0138 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0237 | 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 | a0001c0005t0001g0165 | 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 | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1074-100G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777104 | |||||||
| chr12:46777127 | A | G | 47 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(44): Show |
54 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(51): 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 | a0002c0002t0002g0039 | 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 | a0003c0003t0002g0027 | 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 | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1074-299G>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 12/16 | chr12 | 46777303 | |||||||
| chr12:46777356 | G | A | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): 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 | a0001c0001t0001g0318 | 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 | a0002c0002t0002g0001 a0002c0002t0002g0047 a0002c0002t0002g0048 others(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 | 110 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): 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 | a0006c0017t0002g0164 | 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 | a0002c0002t0002g0039 | 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 | 273 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(270): Show |
307 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(304): 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 | a0001c0001t0002g0299 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0211 |
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 | a0001c0001t0009g0099 a0003c0003t0002g0019 a0003c0003t0002g0027 others(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 | a0001c0001t0001g0213 a0001c0001t0001g0241 a0003c0003t0002g0019 others(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 | a0003c0003t0002g0268 | 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 | 270 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
304 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(301): 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 | a0008c0014t0001g0221 | 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 | a0001c0001t0001g0087 a0001c0001t0006g0330 a0001c0001t0006g0331 others(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 | a0001c0001t0008g0276 a0001c0001t0008g0277 a0001c0001t0008g0279 |
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 | 185 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
212 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(209): 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 | a0001c0001t0001g0031 a0001c0001t0001g0138 a0001c0001t0001g0291 others(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 | a0004c0004t0002g0064 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0091 a0001c0001t0001g0301 |
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 | a0001c0001t0001g0138 a0001c0001t0003g0017 a0001c0001t0003g0092 others(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 | a0001c0001t0002g0255 a0002c0002t0001g0078 a0002c0002t0002g0001 others(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 | 58 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(55): Show |
65 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(62): 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 | a0001c0001t0001g0088 | 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 | 110 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): 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 | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0107 | 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 | a0002c0002t0002g0056 a0013c0007t0011g0059 |
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 | a0001c0005t0015g0081 | 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 | a0003c0003t0002g0244 a0003c0003t0002g0268 a0003c0003t0002g0269 others(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 | a0001c0001t0005g0082 a0001c0001t0005g0083 |
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 | a0001c0001t0006g0334 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0118 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0091 |
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 | a0001c0001t0002g0036 | 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 | a0001c0001t0004g0320 a0001c0001t0004g0322 a0001c0001t0004g0329 |
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 | a0003c0003t0002g0019 a0003c0003t0002g0027 a0003c0003t0002g0029 others(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 | a0001c0001t0001g0032 a0001c0001t0002g0287 a0001c0001t0002g0298 others(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 | a0004c0004t0002g0055 | 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 | a0001c0001t0002g0267 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0091 |
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 | a0002c0002t0002g0049 | 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 | 57 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(54): Show |
63 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(60): 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 | a0003c0003t0002g0019 a0003c0003t0002g0027 a0003c0003t0002g0029 others(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 | 111 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(108): 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 | |||||||
| chr12:46782953 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0002g0298 |
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 | a0001c0001t0001g0091 a0001c0001t0001g0138 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0326 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0175 others(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 |
34 | a0001c0001t0001g0087 a0001c0001t0001g0100 a0001c0001t0001g0140 others(31): Show |
34 | HG01099.hp1 HG01099.hp2 HG01516.hp1 others(31): 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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0207 a0001c0001t0002g0267 a0001c0001t0004g0309 others(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 | a0001c0001t0005g0028 a0001c0001t0005g0258 |
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 | a0001c0001t0001g0088 | 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 | a0001c0005t0015g0081 a0003c0003t0002g0244 a0003c0003t0002g0270 others(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 | a0001c0001t0010g0166 a0001c0001t0010g0168 a0001c0001t0016g0169 |
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 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0008c0014t0001g0221 |
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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(80): 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 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0200 a0001c0001t0008g0279 |
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 | a0001c0001t0001g0196 a0001c0001t0008g0276 a0001c0001t0008g0277 |
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 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0232 |
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 | a0001c0001t0001g0231 | 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 | a0002c0002t0001g0086 | 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 | 81 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(78): 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 | a0001c0001t0001g0104 a0001c0001t0001g0122 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0203 a0001c0001t0001g0242 |
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 | 62 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0020 others(59): Show |
68 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(65): 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 | a0001c0001t0001g0088 a0001c0001t0003g0214 a0001c0001t0004g0316 others(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 | a0001c0001t0001g0013 a0002c0002t0001g0078 a0002c0002t0002g0009 others(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 | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.493+1235delC | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 7/16 | chr12 | 46783306 | |||||||
| chr12:46783461 | C | A | 18 | a0001c0001t0005g0028 a0001c0001t0005g0037 a0001c0001t0005g0038 others(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 | a0001c0001t0001g0301 | 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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
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 | a0001c0001t0001g0013 a0003c0003t0002g0019 a0003c0003t0002g0027 others(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 | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): 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 | a0001c0001t0001g0157 a0001c0001t0001g0161 |
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 | a0002c0002t0012g0068 a0002c0002t0013g0115 |
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 | a0001c0001t0001g0224 | 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 | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
194 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(191): 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 | a0002c0002t0002g0050 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.327-119C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 5/16 | chr12 | 46785296 | |||||||
| chr12:46785471 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0002g0287 a0001c0001t0002g0298 others(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 | 246 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(243): Show |
279 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(276): 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 | a0001c0001t0004g0327 | 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 | a0002c0002t0001g0070 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0272 a0001c0005t0001g0302 |
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 | a0001c0001t0001g0148 | 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 | a0001c0001t0002g0292 a0001c0001t0006g0335 a0002c0002t0002g0054 others(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 | a0001c0001t0010g0166 a0001c0001t0010g0168 a0001c0001t0016g0169 |
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 | 224 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): 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 | CTTTTTTT others(1): Show |
C | 13 | a0001c0001t0001g0031 a0001c0001t0001g0291 a0001c0001t0003g0288 others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0175 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0181 a0003c0003t0002g0206 |
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 | a0003c0003t0002g0282 | 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 | 47 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(44): Show |
54 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(51): 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 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0291 |
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 | a0002c0002t0002g0052 | 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 | 25 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(22): 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 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
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 | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
187 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(184): 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 | a0001c0001t0001g0108 a0001c0001t0001g0117 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0118 | 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 | a0001c0005t0001g0302 | 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 | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(15): 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 | a0002c0002t0001g0012 a0002c0002t0001g0060 a0002c0002t0001g0070 others(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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | a0003c0003t0002g0219 a0003c0003t0002g0220 |
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 | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(15): 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 | a0001c0001t0001g0013 a0001c0001t0001g0159 a0001c0001t0003g0092 others(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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0318 a0001c0001t0003g0315 a0001c0001t0004g0007 others(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 | a0001c0005t0001g0302 | 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 | a0002c0002t0001g0012 a0002c0002t0001g0060 a0002c0002t0001g0070 others(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 | a0002c0002t0001g0012 a0002c0002t0001g0060 a0002c0002t0001g0070 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0300 a0001c0001t0001g0304 others(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 | a0002c0002t0013g0115 | 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 | a0001c0001t0001g0114 | 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 | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(15): 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 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0291 others(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 | a0003c0003t0002g0280 | 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 | a0001c0001t0001g0091 | 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 | a0003c0003t0002g0244 a0011c0009t0002g0245 |
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 | a0001c0001t0003g0132 a0001c0001t0003g0192 a0001c0001t0003g0204 others(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 | a0001c0001t0001g0118 a0001c0001t0006g0330 a0001c0001t0006g0333 others(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 | a0003c0003t0002g0029 | 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 | a0001c0005t0001g0165 a0006c0017t0002g0164 |
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 | a0001c0001t0001g0091 | 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 | a0002c0002t0001g0012 a0002c0002t0001g0060 a0002c0002t0001g0070 others(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 | a0003c0003t0002g0244 a0011c0009t0002g0245 |
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 | a0001c0005t0015g0081 | 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 | 328 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(325): Show |
375 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(372): 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 | a0002c0002t0002g0085 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | a0001c0001t0006g0335 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | 82 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0030 others(79): 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 | a0001c0001t0008g0276 a0001c0001t0008g0277 a0001c0001t0008g0279 others(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 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0200 others(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 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0200 others(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 | a0011c0009t0002g0245 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0300 a0001c0001t0001g0301 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0291 others(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 | a0002c0002t0002g0079 | 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 | a0001c0001t0001g0138 | 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 | a0001c0005t0001g0302 a0002c0002t0001g0012 a0002c0002t0001g0051 others(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 | a0002c0002t0002g0039 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0118 | 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 | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(15): 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 | a0001c0001t0001g0091 | 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 | a0002c0002t0012g0068 | 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 | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(15): 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0318 a0001c0001t0003g0315 a0001c0001t0004g0007 others(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 | a0002c0002t0001g0012 a0002c0002t0001g0051 a0002c0002t0001g0060 others(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 | a0002c0002t0013g0115 | 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 | 137 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0030 others(134): 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 | a0001c0005t0015g0081 | 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 | a0001c0005t0001g0302 | 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 | a0001c0001t0003g0132 a0001c0001t0003g0192 a0001c0001t0003g0204 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0300 a0001c0001t0001g0301 others(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 | a0003c0003t0002g0265 | 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 | 327 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(324): Show |
374 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(371): 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 | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
174 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(171): 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 | a0002c0002t0001g0012 a0002c0002t0001g0051 a0002c0002t0001g0060 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0291 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0158 | 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 | a0002c0002t0001g0012 a0002c0002t0001g0051 a0002c0002t0001g0060 others(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 | a0001c0001t0005g0186 a0008c0014t0001g0221 |
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 | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(15): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0256 a0001c0001t0001g0261 |
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 | a0002c0002t0012g0068 a0002c0002t0013g0115 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | a0002c0002t0001g0012 a0002c0002t0001g0051 a0002c0002t0001g0060 others(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 | a0001c0001t0003g0240 | 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 | a0001c0001t0006g0335 | 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 | a0002c0002t0002g0052 | 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 | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(15): 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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | 3 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 |
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 | a0004c0004t0002g0055 | 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 | a0001c0005t0001g0302 a0002c0002t0001g0012 a0002c0002t0001g0051 others(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 | a0001c0001t0002g0128 | 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 | a0002c0002t0001g0012 a0002c0002t0001g0051 a0002c0002t0001g0060 others(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 | 137 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0030 others(134): 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 | a0003c0003t0002g0253 | 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 | a0001c0005t0001g0165 | 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 | a0001c0001t0001g0016 | 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 | a0001c0005t0001g0302 | 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 | a0002c0002t0001g0012 a0002c0002t0001g0051 a0002c0002t0001g0060 others(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 | a0001c0001t0008g0279 | 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 | a0002c0002t0013g0115 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0291 others(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 | a0001c0005t0001g0302 | 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 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
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 | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(15): 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 | a0002c0002t0013g0115 | 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 | 162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
183 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(180): 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 | a0001c0001t0001g0032 a0001c0001t0002g0287 a0001c0001t0002g0298 others(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 | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(15): 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 | a0002c0002t0002g0067 | 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 | a0002c0002t0001g0012 a0002c0002t0001g0051 a0002c0002t0001g0060 others(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 | 198 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
221 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(218): 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 | a0002c0002t0002g0052 | 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0256 a0001c0001t0001g0261 |
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 | a0001c0001t0003g0297 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0300 a0001c0001t0001g0301 others(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 | a0001c0001t0002g0255 | 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 | 333 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(330): Show |
380 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(377): Show |
intron_variant | MODIFIER | c.-112-4514A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46797697 | |||||||
| chr12:46797709 | C | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(15): 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 | 162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
183 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(180): 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 | a0014c0013t0001g0190 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0301 | 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 | 333 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(330): Show |
380 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(377): 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 | a0001c0005t0001g0165 a0006c0017t0002g0164 |
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 | a0001c0001t0001g0087 a0001c0001t0006g0330 a0001c0001t0006g0331 others(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 | a0001c0001t0001g0104 | 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 | a0005c0006t0001g0071 a0005c0006t0001g0072 |
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 | a0003c0003t0002g0253 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0251 others(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 | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(15): 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 | a0001c0001t0003g0228 | 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 | a0001c0001t0001g0131 | 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 | a0001c0005t0001g0302 | 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 | a0002c0002t0002g0162 | 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 | a0001c0001t0001g0145 a0001c0001t0001g0207 |
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 | 188 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
210 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(207): 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 | a0001c0001t0001g0032 a0001c0001t0001g0300 a0001c0001t0001g0301 others(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 | a0001c0005t0001g0165 a0001c0005t0015g0081 a0006c0017t0002g0164 |
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 | a0001c0001t0001g0087 a0001c0001t0006g0330 a0001c0001t0006g0331 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0251 others(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 | a0001c0001t0008g0276 a0001c0001t0008g0277 a0001c0001t0008g0279 others(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 | a0003c0003t0002g0275 | 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 | a0003c0003t0002g0314 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0105 a0001c0001t0001g0106 others(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 | a0002c0002t0002g0076 | 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 | 17 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(14): 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 | a0001c0001t0005g0208 a0001c0001t0005g0209 |
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 | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
211 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.-113+2654C>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46800949 | |||||||
| chr12:46800974 | T | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(14): 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 | a0002c0002t0001g0073 | 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 | a0001c0005t0001g0302 | 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 | 163 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
184 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(181): Show |
intron_variant | MODIFIER | c.-113+2481G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801122 | |||||||
| chr12:46801273 | G | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(14): 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 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0228 |
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 | 17 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(14): 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 | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
211 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.-113+2097G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46801506 | |||||||
| chr12:46801632 | A | G | 17 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(14): 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 | a0001c0005t0001g0165 a0001c0005t0015g0081 a0006c0017t0002g0164 |
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 | a0001c0001t0001g0032 a0001c0001t0001g0300 a0001c0001t0001g0301 others(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 | a0003c0003t0002g0282 | 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 | a0001c0001t0002g0267 a0003c0003t0002g0268 |
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 | a0001c0001t0002g0292 a0001c0001t0006g0335 |
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 | a0002c0002t0001g0086 | 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 | a0001c0001t0001g0301 | 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 | a0001c0005t0015g0081 | 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 | 280 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(277): Show |
313 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.-113+997A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802606 | |||||||
| chr12:46802678 | C | T | 281 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(278): Show |
314 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(311): Show |
intron_variant | MODIFIER | c.-113+925G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 2/16 | chr12 | 46802678 | |||||||
| chr12:46802722 | A | G | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
211 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(208): 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 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
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 | 17 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(14): 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 | a0002c0002t0001g0012 a0002c0002t0001g0051 a0002c0002t0001g0060 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0301 | 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 | a0001c0005t0001g0165 a0001c0005t0015g0081 a0006c0017t0002g0164 |
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 | a0001c0001t0001g0207 | 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 | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
211 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(208): 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 | a0004c0004t0002g0199 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0251 others(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 | 17 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(14): 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 | 333 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(330): Show |
380 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(377): 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 | a0001c0001t0001g0117 | 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 | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
211 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(208): 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 | a0001c0001t0003g0288 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0300 a0001c0001t0001g0301 others(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 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0041 others(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 | a0001c0001t0008g0279 | 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 | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
211 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.-304-1132A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46804926 | |||||||
| chr12:46805053 | C | T | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
211 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.-304-1259G>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46805053 | |||||||
| chr12:46805073 | C | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(13): 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 | a0001c0001t0010g0166 a0001c0001t0010g0168 a0001c0001t0016g0169 |
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 | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
211 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(208): 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 | a0001c0001t0002g0299 | 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 | a0006c0017t0002g0164 | 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 | a0001c0001t0002g0292 a0001c0001t0006g0335 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0172 a0001c0001t0001g0173 others(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 | a0001c0005t0001g0165 a0006c0017t0002g0164 |
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 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
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 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | 16 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0040 others(13): 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 | a0003c0003t0002g0314 | 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 | a0008c0014t0001g0221 | 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 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0002g0292 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0318 a0001c0001t0001g0325 others(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 | 288 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
320 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(317): 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 | a0001c0001t0001g0146 | 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 | a0003c0003t0002g0244 a0011c0009t0002g0245 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0087 others(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 | a0002c0002t0002g0085 | 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0318 a0001c0001t0001g0325 others(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 | a0002c0002t0002g0069 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0318 a0001c0001t0001g0325 others(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 | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(38): 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 | 169 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(166): Show |
199 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.-304-4096delG | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46807889 | |||||||
| chr12:46807889 | ACC | A | 38 | a0001c0001t0001g0091 a0001c0001t0001g0261 a0001c0001t0001g0318 others(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 | a0001c0001t0005g0129 | 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 | 144 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(141): Show |
172 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(169): 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 | a0001c0001t0010g0166 a0001c0001t0010g0168 a0001c0001t0016g0169 others(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 | a0001c0001t0002g0287 a0001c0001t0002g0292 a0001c0001t0003g0289 |
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 | a0001c0001t0003g0297 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0127 a0001c0001t0001g0170 |
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 | 223 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0016 others(220): Show |
257 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.-304-4730dupT | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46808523 | |||||||
| chr12:46808612 | C | G | 15 | a0001c0001t0003g0315 a0001c0001t0004g0007 a0001c0001t0004g0308 others(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 | a0001c0001t0003g0192 a0001c0001t0003g0204 a0001c0001t0017g0193 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0318 a0001c0001t0001g0325 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0197 a0001c0001t0001g0198 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0254 | 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 | a0001c0001t0010g0166 a0001c0001t0010g0168 a0001c0001t0016g0169 others(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 | a0003c0003t0002g0269 | 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 | 251 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0016 others(248): Show |
289 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(286): 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 | a0001c0001t0001g0091 a0001c0001t0001g0318 a0001c0001t0001g0325 others(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 | 87 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(84): Show |
100 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(97): 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 | a0001c0001t0001g0091 a0001c0001t0001g0318 a0001c0001t0001g0325 others(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 | a0004c0004t0002g0199 | 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0318 a0001c0001t0001g0325 others(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 | a0002c0002t0002g0074 a0002c0002t0002g0075 a0002c0002t0002g0076 |
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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0300 a0001c0001t0001g0301 others(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 | a0001c0001t0003g0289 | 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 | a0001c0010t0001g0323 a0003c0003t0002g0314 |
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 | a0001c0001t0006g0335 a0001c0001t0019g0336 |
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 | a0001c0001t0001g0091 a0001c0001t0001g0318 a0001c0001t0001g0325 others(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 | a0001c0001t0005g0082 a0001c0001t0005g0083 a0002c0002t0001g0012 others(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 | a0001c0001t0001g0032 a0001c0001t0002g0298 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0251 others(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 | a0002c0002t0001g0086 a0002c0002t0002g0052 |
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 | a0001c0001t0003g0297 | 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 | a0001c0001t0010g0166 a0001c0001t0010g0168 a0001c0001t0016g0169 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0091 others(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 | a0001c0001t0016g0169 | 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 | a0001c0001t0001g0174 | 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 | 87 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(84): Show |
100 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(97): 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 | a0001c0001t0001g0006 a0001c0001t0001g0197 a0001c0001t0001g0198 |
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 | a0001c0001t0010g0166 a0001c0001t0010g0168 a0001c0001t0016g0169 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0148 | 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 | a0002c0002t0001g0051 | 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 | a0001c0001t0009g0099 | 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 | 251 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0016 others(248): Show |
289 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(286): 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 | a0001c0001t0001g0091 a0001c0001t0001g0318 a0001c0001t0001g0325 others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0318 a0001c0001t0001g0325 others(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 | a0003c0003t0002g0275 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0008g0279 | 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 | a0003c0003t0002g0284 | 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 | 251 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0016 others(248): Show |
289 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(286): 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0087 a0001c0001t0005g0082 a0001c0001t0005g0083 others(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 | a0001c0001t0005g0082 a0001c0001t0005g0083 |
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 | a0003c0003t0002g0270 | 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0100 | 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 | 35 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(32): 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 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0160 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0161 a0001c0001t0001g0252 others(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 | a0001c0001t0001g0262 a0001c0001t0001g0301 a0001c0001t0001g0318 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0325 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0172 a0001c0001t0001g0173 others(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 | 65 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(62): Show |
77 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(74): 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 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0224 others(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 | a0001c0001t0001g0091 a0006c0017t0002g0164 |
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 | a0001c0005t0001g0165 | 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 | a0001c0001t0001g0087 a0001c0001t0005g0082 a0001c0001t0005g0083 others(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 | a0002c0002t0001g0078 a0002c0002t0002g0079 |
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 | a0002c0002t0001g0077 a0002c0002t0001g0080 |
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 | a0001c0001t0019g0336 | 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 | a0001c0005t0015g0081 | 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 | a0001c0001t0006g0335 | 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 | a0001c0001t0002g0267 a0003c0003t0002g0280 |
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 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0256 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0304 a0001c0001t0002g0298 others(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 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0088 a0001c0001t0005g0043 |
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 | 216 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
245 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(242): 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 | a0001c0001t0001g0114 a0001c0001t0001g0120 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0090 a0001c0001t0001g0104 a0001c0001t0001g0126 |
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 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0005g0042 |
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 | a0001c0001t0005g0041 | 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 | a0001c0001t0010g0166 a0001c0001t0010g0168 a0001c0001t0016g0169 others(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 | a0001c0001t0001g0091 | 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 | a0003c0003t0002g0280 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-305+10391T>C | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46815512 | |||||||
| chr12:46815548 | T | A | 1 | a0001c0001t0001g0236 | 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 | a0001c0001t0002g0255 | 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 | a0002c0002t0002g0050 | 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 | 39 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0044 others(36): 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 | a0003c0003t0002g0269 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0291 a0001c0001t0002g0267 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | 73 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0044 others(70): 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 | a0001c0001t0001g0087 a0001c0001t0005g0082 a0001c0001t0005g0083 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0091 others(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 | a0001c0001t0005g0082 a0001c0001t0005g0083 |
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 | a0001c0001t0003g0294 | 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 | 251 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0016 others(248): Show |
289 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.-305+8506dupA | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46817396 | |||||||
| chr12:46817516 | C | T | 1 | a0001c0001t0009g0099 | 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 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0088 | 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 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0228 |
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 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0003g0315 others(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 | a0001c0001t0001g0185 a0001c0001t0005g0184 |
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 | a0001c0001t0010g0166 | 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 | 100 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(97): Show |
114 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(111): 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 | a0003c0003t0002g0265 | 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 | a0001c0001t0002g0292 | 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 | a0001c0001t0001g0087 a0001c0001t0006g0330 a0001c0001t0006g0331 others(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 | a0001c0001t0001g0318 a0001c0001t0001g0325 a0001c0001t0001g0326 others(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 | 143 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(140): Show |
161 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(158): 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 | a0001c0001t0004g0327 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0300 a0001c0001t0001g0301 others(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 | a0001c0001t0010g0166 a0001c0001t0010g0168 a0001c0001t0016g0169 others(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 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
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 | a0001c0001t0008g0276 | 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 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(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 | 251 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0016 others(248): Show |
289 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(286): 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 | a0001c0001t0001g0091 | 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 | 59 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0044 others(56): 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 | 144 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(141): Show |
162 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-305+5465A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820438 | |||||||
| chr12:46820509 | T | C | 169 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(166): Show |
191 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.-305+5394A>G | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820509 | |||||||
| chr12:46820590 | G | T | 143 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(140): Show |
161 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(158): 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 | a0001c0001t0001g0091 a0001c0001t0003g0092 |
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 | a0001c0001t0001g0233 | 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 | 251 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0016 others(248): Show |
289 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.-305+5170G>T | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46820733 | |||||||
| chr12:46820787 | C | T | 143 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(140): Show |
161 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(158): 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 | a0001c0001t0010g0166 a0001c0001t0010g0168 a0001c0001t0016g0169 others(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 | a0002c0002t0002g0001 a0002c0002t0002g0047 a0002c0002t0002g0048 others(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 | a0002c0002t0002g0084 a0002c0002t0002g0085 |
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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0318 a0001c0001t0001g0325 a0001c0001t0001g0326 others(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 | a0001c0001t0001g0091 | 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 | 11 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0044 others(8): 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 | a0002c0002t0002g0162 | 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 | a0001c0001t0004g0329 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0300 a0001c0001t0001g0301 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0010g0166 a0001c0001t0010g0168 a0001c0001t0016g0169 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0291 |
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 | a0001c0001t0005g0171 | 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 | a0002c0002t0002g0039 | 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 | a0002c0002t0001g0086 | 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 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0318 a0001c0001t0001g0325 a0001c0001t0001g0326 others(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 | a0001c0001t0001g0266 | 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 | 169 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(166): Show |
191 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(188): 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 | a0001c0001t0001g0091 | 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 | a0003c0003t0002g0314 | 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 | a0001c0001t0002g0303 | 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 | a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | 169 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(166): Show |
191 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(188): 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 | a0001c0001t0003g0297 | 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 | a0001c0001t0001g0236 | 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 | 143 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(140): Show |
161 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(158): 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 | a0001c0001t0001g0030 a0001c0001t0001g0251 a0001c0001t0001g0252 others(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 | a0001c0001t0001g0087 a0001c0001t0006g0330 a0001c0001t0006g0331 others(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 | 169 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(166): Show |
191 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.-305+1746T>A | SLC38A4 | ENSG00000139209.16 | transcript | ENST00000266579.9 | protein_coding | 1/16 | chr12 | 46824157 | |||||||
| chr12:46824361 | G | T | 169 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(166): Show |
191 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(188): 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0089 | 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 | 67 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0044 others(64): 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 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0261 a0001c0001t0001g0262 others(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 | a0001c0001t0004g0327 | 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 | a0001c0001t0003g0296 | 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 | 79 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(76): Show |
92 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(89): 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 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0254 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0272 a0001c0001t0002g0036 others(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 | a0003c0003t0002g0284 a0010c0018t0002g0285 |
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 | a0003c0003t0002g0286 | 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 | a0001c0001t0002g0287 | 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 | a0001c0001t0001g0031 a0001c0001t0004g0313 a0002c0002t0014g0312 |
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 | a0001c0001t0003g0288 a0001c0001t0003g0289 a0001c0001t0003g0315 others(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 | a0001c0001t0004g0317 a0007c0015t0003g0290 |
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 | a0001c0001t0001g0291 a0001c0001t0001g0318 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0003g0294 others(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 | a0001c0001t0004g0035 a0001c0001t0004g0328 |
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 | a0001c0001t0003g0295 | 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 | a0001c0001t0004g0329 | 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 | a0001c0001t0001g0304 | 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 | a0001c0001t0004g0308 a0001c0001t0004g0309 a0001c0001t0004g0310 others(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 | a0001c0001t0004g0308 a0001c0001t0004g0309 a0001c0001t0004g0310 others(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 | a0001c0001t0002g0036 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0300 a0001c0001t0001g0301 others(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 | a0001c0001t0001g0318 a0001c0001t0001g0325 a0001c0001t0001g0326 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0305 a0001c0001t0001g0306 others(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 |