Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6519 |
| ensemblid | ENSG00000138079.14 |
| hgncid | 11025 |
| symbol | SLC3A1 |
| name | solute carrier family 3 member 1 |
| refseq_nuc | NM_000341.4 |
| refseq_prot | NP_000332.2 |
| ensembl_nuc | ENST00000260649.11 |
| ensembl_prot | ENSP00000260649.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 44275480 |
| end | 44321494 |
| strand | + |
| ver | v1.2 |
| region | chr2:44275480-44321494 |
| region5000 | chr2:44270480-44326494 |
| regionname0 | SLC3A1_chr2_44275480_44321494 |
| regionname5000 | SLC3A1_chr2_44270480_44326494 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 685 | 200 | 78 | 38 | 65 | 4 | 14 | 50 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | MAEDK others(680): Show |
chr2 | 44270480 | 44326494 |
| a0002 | 0/1 | 685 | 143 | 16 | 34 | 61 | 10 | 21 | 48 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | MAEDK others(680): Show |
chr2 | 44270480 | 44326494 |
| a0003 | 0/0 | 685 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | MAEDK others(680): Show |
chr2 | 44270480 | 44326494 |
| a0004 | 0/0 | 685 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | MAEDK others(680): Show |
chr2 | 44270480 | 44326494 |
| a0005 | 0/0 | 685 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | MAEDK others(680): Show |
chr2 | 44270480 | 44326494 |
| a0006 | 0/0 | 685 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | MAEDK others(680): Show |
chr2 | 44270480 | 44326494 |
| a0007 | 0/0 | 685 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | MAEDK others(680): Show |
chr2 | 44270480 | 44326494 |
| a0008 | 0/0 | 685 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | MAEDK others(680): Show |
chr2 | 44270480 | 44326494 |
| a0009 | 0/0 | 685 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | MAEDK others(680): Show |
chr2 | 44270480 | 44326494 |
| a0010 | 0/0 | 685 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | MAEDK others(680): Show |
chr2 | 44270480 | 44326494 |
| a0011 | 0/0 | 685 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | MAEDK others(680): Show |
chr2 | 44270480 | 44326494 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 2055 | 103 | 13 | 26 | 57 | 1 | 5 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0001c0003 | 0/0 | 2055 | 95 | 63 | 12 | 8 | 3 | 9 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0001c0017 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0001c0018 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0002c0001 | 0/1 | 2055 | 134 | 10 | 32 | 60 | 10 | 21 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0002c0004 | 0/0 | 2055 | 6 | 4 | 1 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0002c0010 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0002c0013 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0002c0016 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0003c0005 | 0/0 | 2055 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0004c0006 | 0/0 | 2055 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0005c0008 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0006c0009 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0007c0011 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0008c0014 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0009c0015 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0010c0007 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 | ||
| a0011c0012 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ATGGC others(2050): Show |
chr2 | 44270480 | 44326494 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 2969 | 8 | 6 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0002t0002 | 1/0 | 2969 | 88 | 5 | 20 | 56 | 1 | 5 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0002t0003 | 0/0 | 2969 | 6 | 1 | 4 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0002t0009 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0003t0001 | 0/0 | 2969 | 40 | 34 | 5 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0003t0002 | 0/0 | 2969 | 10 | 2 | 1 | 6 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0003t0003 | 0/0 | 2969 | 21 | 5 | 5 | 1 | 1 | 9 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0003t0004 | 0/0 | 2969 | 19 | 18 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0003t0006 | 0/0 | 2969 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0003t0011 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0003t0012 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0003t0013 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0017t0007 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0001c0018t0003 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0002c0001t0001 | 0/1 | 2969 | 128 | 7 | 30 | 60 | 10 | 20 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0002c0001t0005 | 0/0 | 2969 | 4 | 2 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0002c0001t0008 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0002c0001t0010 | 0/0 | 2969 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0002c0004t0001 | 0/0 | 2969 | 6 | 4 | 1 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0002c0010t0001 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0002c0013t0001 | 0/0 | 2969 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0002c0016t0001 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0003c0005t0002 | 0/0 | 2969 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0004c0006t0001 | 0/0 | 2969 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0005c0008t0002 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0006c0009t0002 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0007c0011t0004 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0008c0014t0001 | 0/0 | 2969 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0009c0015t0001 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0010c0007t0002 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| a0011c0012t0001 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | ACTCT others(2964): Show |
chr2 | 44270480 | 44326494 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0001 | 1/0 | 6 | 1 | 0 | 4 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0002t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0006g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0011g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0012g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0003t0013g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0017t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0001c0018t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0001t0010g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0004t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0010t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0013t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0002c0016t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0003c0005t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0003c0005t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0004c0006t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0004c0006t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0005c0008t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0006c0009t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0007c0011t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0008c0014t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0009c0015t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0010c0007t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| a0011c0012t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0275 | EUR | GBR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00099 | hp2 | a0002 | c0001 | t0001 | g0067 | EUR | GBR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00280 | hp1 | a0001 | c0003 | t0003 | g0111 | EUR | FIN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00280 | hp2 | a0002 | c0001 | t0001 | g0088 | EUR | FIN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0272 | EUR | FIN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0242 | EUR | FIN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0052 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00597 | hp1 | a0002 | c0001 | t0001 | g0068 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0128 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0073 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00621 | hp2 | a0005 | c0008 | t0002 | g0193 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00639 | hp1 | a0001 | c0003 | t0003 | g0314 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0148 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00642 | hp2 | a0002 | c0001 | t0001 | g0302 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00733 | hp1 | a0002 | c0001 | t0001 | g0273 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0204 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00735 | hp2 | a0002 | c0001 | t0001 | g0030 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00738 | hp1 | a0001 | c0003 | t0003 | g0277 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0303 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01069 | hp1 | a0002 | c0001 | t0001 | g0096 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01069 | hp2 | a0002 | c0001 | t0001 | g0090 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01070 | hp1 | a0002 | c0001 | t0001 | g0269 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01070 | hp2 | a0001 | c0003 | t0003 | g0320 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01071 | hp1 | a0002 | c0001 | t0001 | g0271 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0091 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0141 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0185 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01081 | hp2 | a0002 | c0001 | t0001 | g0097 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0188 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01109 | hp1 | a0002 | c0001 | t0001 | g0274 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01109 | hp2 | a0001 | c0003 | t0004 | g0289 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01167 | hp1 | a0002 | c0001 | t0001 | g0135 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0213 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01168 | hp1 | a0002 | c0001 | t0005 | g0063 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0055 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01169 | hp1 | a0002 | c0001 | t0005 | g0064 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0216 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01192 | hp1 | a0001 | c0003 | t0003 | g0305 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01192 | hp2 | a0002 | c0001 | t0001 | g0318 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0028 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01243 | hp2 | a0002 | c0004 | t0001 | g0172 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01256 | hp1 | a0002 | c0001 | t0001 | g0116 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0017 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0210 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01257 | hp2 | a0002 | c0001 | t0001 | g0115 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01258 | hp1 | a0002 | c0001 | t0001 | g0114 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01258 | hp2 | a0001 | c0002 | t0003 | g0017 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0031 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0177 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01358 | hp1 | a0002 | c0001 | t0001 | g0140 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0113 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0260 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0071 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01496 | hp1 | a0002 | c0001 | t0001 | g0112 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0259 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01516 | hp1 | a0002 | c0001 | t0001 | g0268 | EUR | IBS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0163 | EUR | IBS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01517 | hp1 | a0002 | c0001 | t0001 | g0270 | EUR | IBS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01517 | hp2 | a0002 | c0001 | t0001 | g0004 | EUR | IBS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01884 | hp1 | a0001 | c0003 | t0013 | g0293 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01884 | hp2 | a0001 | c0003 | t0004 | g0280 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01891 | hp1 | a0001 | c0003 | t0004 | g0283 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01928 | hp1 | a0001 | c0003 | t0002 | g0019 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0220 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0207 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0144 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01943 | hp1 | a0002 | c0001 | t0001 | g0049 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0246 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01952 | hp1 | a0002 | c0001 | t0001 | g0092 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0186 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0079 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0241 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0221 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0066 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG01993 | hp2 | a0002 | c0013 | t0001 | g0004 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0215 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02015 | hp1 | a0001 | c0003 | t0003 | g0307 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02040 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02040 | hp2 | a0001 | c0003 | t0002 | g0119 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02055 | hp1 | a0001 | c0017 | t0007 | g0162 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02055 | hp2 | a0002 | c0001 | t0001 | g0065 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0152 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0089 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0151 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02074 | hp2 | a0006 | c0009 | t0002 | g0100 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0101 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0134 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02145 | hp1 | a0002 | c0001 | t0001 | g0056 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02145 | hp2 | a0001 | c0003 | t0004 | g0287 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0245 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02148 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | CDX | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | CDX | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02165 | hp1 | a0002 | c0001 | t0001 | g0074 | EAS | CDX | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02165 | hp2 | a0002 | c0001 | t0001 | g0059 | EAS | CDX | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0255 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02257 | hp2 | a0001 | c0003 | t0004 | g0291 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02258 | hp1 | a0001 | c0003 | t0003 | g0300 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02258 | hp2 | a0001 | c0002 | t0003 | g0184 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02280 | hp1 | a0002 | c0001 | t0001 | g0087 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0206 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02451 | hp1 | a0007 | c0011 | t0004 | g0016 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02451 | hp2 | a0001 | c0003 | t0004 | g0296 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0137 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02572 | hp1 | a0001 | c0003 | t0004 | g0053 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02572 | hp2 | a0001 | c0003 | t0004 | g0299 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02602 | hp1 | a0002 | c0001 | t0001 | g0018 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02602 | hp2 | a0001 | c0003 | t0003 | g0308 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02615 | hp2 | a0001 | c0003 | t0002 | g0258 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0254 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02630 | hp2 | a0001 | c0003 | t0004 | g0278 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02647 | hp2 | a0002 | c0004 | t0001 | g0171 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02683 | hp1 | a0001 | c0003 | t0003 | g0306 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0014 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02698 | hp1 | a0001 | c0003 | t0003 | g0311 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02698 | hp2 | a0008 | c0014 | t0001 | g0319 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0039 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02717 | hp2 | a0002 | c0001 | t0001 | g0023 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0037 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02809 | hp2 | a0001 | c0003 | t0004 | g0288 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02886 | hp1 | a0002 | c0016 | t0001 | g0161 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02897 | hp1 | a0001 | c0003 | t0006 | g0266 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02922 | hp1 | a0001 | c0003 | t0012 | g0292 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0248 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02970 | hp1 | a0001 | c0003 | t0004 | g0297 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02970 | hp2 | a0002 | c0001 | t0001 | g0104 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02976 | hp1 | a0001 | c0003 | t0006 | g0285 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0178 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0146 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03017 | hp2 | a0001 | c0003 | t0003 | g0310 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03041 | hp1 | a0001 | c0003 | t0004 | g0281 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0284 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0250 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0243 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03139 | hp2 | a0001 | c0003 | t0004 | g0298 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03195 | hp1 | a0009 | c0015 | t0001 | g0252 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0036 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0257 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03225 | hp2 | a0001 | c0003 | t0004 | g0282 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0317 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03239 | hp2 | a0002 | c0001 | t0001 | g0145 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03453 | hp1 | a0002 | c0001 | t0001 | g0026 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0166 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0253 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03486 | hp2 | a0002 | c0001 | t0001 | g0025 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03490 | hp1 | a0001 | c0003 | t0003 | g0313 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0239 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03492 | hp1 | a0002 | c0001 | t0001 | g0093 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0240 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0251 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03540 | hp1 | a0002 | c0001 | t0008 | g0105 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03579 | hp1 | a0002 | c0004 | t0001 | g0173 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03579 | hp2 | a0001 | c0003 | t0004 | g0290 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0125 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0086 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03688 | hp1 | a0002 | c0001 | t0001 | g0051 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03688 | hp2 | a0001 | c0003 | t0003 | g0315 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03704 | hp1 | a0001 | c0003 | t0003 | g0312 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0133 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03831 | hp1 | a0002 | c0001 | t0001 | g0136 | SAS | BEB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0095 | SAS | BEB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0033 | SAS | BEB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03927 | hp2 | a0001 | c0003 | t0003 | g0301 | SAS | BEB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03942 | hp1 | a0002 | c0001 | t0001 | g0149 | SAS | BEB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03942 | hp2 | a0002 | c0001 | t0010 | g0316 | SAS | BEB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0034 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG04115 | hp2 | a0002 | c0001 | t0001 | g0020 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG04199 | hp1 | a0002 | c0001 | t0001 | g0085 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG04199 | hp2 | a0002 | c0001 | t0001 | g0022 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0195 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0236 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0143 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG04228 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18522 | hp1 | a0001 | c0003 | t0003 | g0309 | AFR | YRI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18522 | hp2 | a0001 | c0003 | t0004 | g0016 | AFR | YRI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18612 | hp1 | a0002 | c0001 | t0001 | g0081 | EAS | CHB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | CHB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0040 | AFR | YRI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18906 | hp2 | a0001 | c0003 | t0004 | g0286 | AFR | YRI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18942 | hp1 | a0002 | c0001 | t0001 | g0138 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18944 | hp1 | a0001 | c0003 | t0011 | g0118 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18945 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18947 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18948 | hp1 | a0002 | c0001 | t0001 | g0120 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18951 | hp1 | a0010 | c0007 | t0002 | g0203 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18951 | hp2 | a0002 | c0001 | t0001 | g0058 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18952 | hp1 | a0002 | c0001 | t0001 | g0129 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18957 | hp1 | a0001 | c0003 | t0002 | g0084 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18957 | hp2 | a0002 | c0001 | t0001 | g0117 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18959 | hp2 | a0001 | c0003 | t0002 | g0109 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18960 | hp1 | a0002 | c0001 | t0001 | g0157 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18962 | hp2 | a0002 | c0001 | t0001 | g0083 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0057 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18965 | hp2 | a0002 | c0001 | t0001 | g0102 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18966 | hp1 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18966 | hp2 | a0003 | c0005 | t0002 | g0200 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18967 | hp1 | a0003 | c0005 | t0002 | g0201 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0121 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18969 | hp1 | a0004 | c0006 | t0001 | g0045 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0123 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18974 | hp2 | a0002 | c0001 | t0001 | g0070 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18980 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18983 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18984 | hp1 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18985 | hp1 | a0002 | c0001 | t0001 | g0153 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18985 | hp2 | a0001 | c0003 | t0002 | g0103 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18988 | hp1 | a0002 | c0001 | t0001 | g0139 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18988 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18991 | hp2 | a0004 | c0006 | t0001 | g0047 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18993 | hp2 | a0002 | c0001 | t0001 | g0072 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18994 | hp2 | a0002 | c0001 | t0001 | g0076 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA18999 | hp2 | a0002 | c0001 | t0001 | g0107 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19004 | hp2 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19006 | hp1 | a0002 | c0001 | t0001 | g0060 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0080 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19012 | hp1 | a0011 | c0012 | t0001 | g0078 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0294 | AFR | LWK | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | LWK | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | LWK | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0062 | AFR | LWK | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19057 | hp2 | a0002 | c0001 | t0001 | g0108 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19058 | hp1 | a0002 | c0001 | t0001 | g0126 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19058 | hp2 | a0001 | c0002 | t0003 | g0233 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19059 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19059 | hp2 | a0002 | c0001 | t0001 | g0155 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19060 | hp1 | a0002 | c0001 | t0001 | g0046 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19063 | hp2 | a0002 | c0001 | t0001 | g0048 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19064 | hp1 | a0002 | c0001 | t0001 | g0130 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0082 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0098 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19074 | hp2 | a0002 | c0001 | t0001 | g0110 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19076 | hp1 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19076 | hp2 | a0002 | c0001 | t0001 | g0054 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0154 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0147 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19080 | hp2 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19083 | hp1 | a0002 | c0001 | t0001 | g0094 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19084 | hp1 | a0002 | c0001 | t0001 | g0069 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0032 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19091 | hp1 | a0002 | c0004 | t0001 | g0237 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19091 | hp2 | a0002 | c0001 | t0001 | g0122 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19240 | hp1 | a0002 | c0001 | t0005 | g0044 | AFR | YRI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0038 | AFR | YRI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0321 | AFR | ASW | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA20129 | hp2 | a0002 | c0001 | t0005 | g0061 | AFR | ASW | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA20752 | hp1 | a0002 | c0001 | t0001 | g0018 | EUR | TSI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0024 | EUR | TSI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0150 | EUR | TSI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0002 | EUR | TSI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA20905 | hp1 | a0001 | c0003 | t0003 | g0304 | SAS | GIH | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA20905 | hp2 | a0002 | c0001 | t0001 | g0077 | SAS | GIH | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02109 | hp1 | a0001 | c0003 | t0004 | g0276 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02109 | hp2 | a0001 | c0003 | t0004 | g0279 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0295 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02486 | hp2 | a0002 | c0010 | t0001 | g0099 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0249 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0164 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0256 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG06807 | hp1 | a0001 | c0018 | t0003 | g0159 | AFR | USA | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| HG06807 | hp2 | a0002 | c0004 | t0001 | g0170 | AFR | USA | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA20300 | hp1 | a0001 | c0002 | t0009 | g0176 | AFR | USA | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0165 | AFR | USA | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0021 | AFR | LWK | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0267 | AFR | LWK | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0124 | REF | REF | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0001 | REF | REF | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:44275792 | G | A | 1 | a0006 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.257G>A | p.Arg86Gln | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/10 | 313/2969 | 257/2058 | 86/685 | chr2 | 44275792 | |||
| chr2:44275848 | A | G | 1 | a0004 | 2 | NA18969.hp1 NA18991.hp2 |
missense_variant | MODERATE | c.313A>G | p.Ile105Val | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/10 | 369/2969 | 313/2058 | 105/685 | chr2 | 44275848 | |||
| chr2:44301022 | C | T | 1 | a0005 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.1031C>T | p.Ser344Leu | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/10 | 1087/2969 | 1031/2058 | 344/685 | chr2 | 44301022 | |||
| chr2:44301054 | G | A | 1 | a0010 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.1063G>A | p.Val355Met | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/10 | 1119/2969 | 1063/2058 | 355/685 | chr2 | 44301054 | |||
| chr2:44301085 | G | A | 1 | a0007 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1094G>A | p.Arg365Gln | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/10 | 1150/2969 | 1094/2058 | 365/685 | chr2 | 44301085 | |||
| chr2:44304276 | G | C | 1 | a0011 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.1270G>C | p.Val424Leu | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/10 | 1326/2969 | 1270/2058 | 424/685 | chr2 | 44304276 | |||
| chr2:44312587 | T | C | 1 | a0003 | 2 | NA18966.hp2 NA18967.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1334T>C | p.Ile445Thr | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/10 | 1390/2969 | 1334/2058 | 445/685 | chr2 | 44312587 | |||
| chr2:44312643 | G | A | 1 | a0008 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1390G>A | p.Val464Met | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/10 | 1446/2969 | 1390/2058 | 464/685 | chr2 | 44312643 | |||
| chr2:44320427 | G | A | 1 | a0009 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1846G>A | p.Ala616Thr | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 1902/2969 | 1846/2058 | 616/685 | chr2 | 44320427 | |||
| chr2:44320435 | G | A | 4 | a0002 a0004 a0008 others(1): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
missense_variant | MODERATE | c.1854G>A | p.Met618Ile | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 1910/2969 | 1854/2058 | 618/685 | chr2 | 44320435 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:44275649 | A | C | 13 | a0001c0003 a0001c0017 a0001c0018 others(10): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
synonymous_variant | LOW | c.114A>C | p.Gly38Gly | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/10 | 170/2969 | 114/2058 | 38/685 | chr2 | 44275649 | |||
| chr2:44275835 | C | T | 1 | a0001c0018 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.300C>T | p.Leu100Leu | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/10 | 356/2969 | 300/2058 | 100/685 | chr2 | 44275835 | |||
| chr2:44281448 | A | G | 1 | a0001c0017 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.672A>G | p.Gln224Gln | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/10 | 728/2969 | 672/2058 | 224/685 | chr2 | 44281448 | |||
| chr2:44301026 | G | A | 1 | a0002c0010 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1035G>A | p.Glu345Glu | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/10 | 1091/2969 | 1035/2058 | 345/685 | chr2 | 44301026 | |||
| chr2:44312618 | G | A | 1 | a0002c0013 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.1365G>A | p.Ser455Ser | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/10 | 1421/2969 | 1365/2058 | 455/685 | chr2 | 44312618 | |||
| chr2:44313906 | C | T | 1 | a0002c0016 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.1572C>T | p.Asn524Asn | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/10 | 1628/2969 | 1572/2058 | 524/685 | chr2 | 44313906 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:44320770 | T | C | 17 | a0001c0002t0001 a0001c0002t0009 a0001c0003t0001 others(14): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*131T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 131 | chr2 | 44320770 | ||||||
| chr2:44320865 | C | T | 1 | a0002c0001t0010 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*226C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 226 | chr2 | 44320865 | ||||||
| chr2:44320958 | G | T | 4 | a0001c0002t0009 a0001c0003t0006 a0001c0003t0012 others(1): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*319G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 319 | chr2 | 44320958 | ||||||
| chr2:44321143 | T | C | 24 | a0001c0002t0001 a0001c0002t0003 a0001c0002t0009 others(21): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*504T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 504 | chr2 | 44321143 | ||||||
| chr2:44321235 | C | T | 1 | a0002c0001t0005 | 4 | HG01168.hp1 HG01169.hp1 NA19240.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*596C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 596 | chr2 | 44321235 | ||||||
| chr2:44321342 | T | C | 1 | a0001c0017t0007 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*703T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 703 | chr2 | 44321342 | ||||||
| chr2:44321418 | C | T | 2 | a0001c0003t0013 a0002c0001t0008 |
2 | HG01884.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*779C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 779 | chr2 | 44321418 | ||||||
| chr2:44321429 | T | C | 1 | a0001c0002t0009 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*790T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 790 | chr2 | 44321429 | ||||||
| chr2:44321474 | T | C | 18 | a0001c0002t0001 a0001c0003t0001 a0001c0003t0004 others(15): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*835T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 835 | chr2 | 44321474 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:44276040 | A | G | 1 | a0001c0003t0003g0321 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.430+75A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276040 | |||||||
| chr2:44276291 | C | A | 1 | a0001c0003t0002g0019 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.430+326C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276291 | |||||||
| chr2:44276503 | A | G | 22 | a0001c0003t0003g0300 a0001c0003t0003g0301 a0001c0003t0003g0303 others(19): Show |
23 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.430+538A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276503 | |||||||
| chr2:44276520 | A | G | 1 | a0001c0002t0003g0017 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.430+555A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276520 | |||||||
| chr2:44276611 | AGCTACTT others(5): Show |
A | 49 | a0001c0003t0001g0006 a0001c0003t0001g0294 a0001c0003t0001g0295 others(46): Show |
52 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.430+650_430+661del others(12): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44276611 | ||||||
| chr2:44276641 | G | C | 1 | a0001c0003t0004g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.430+676G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276641 | |||||||
| chr2:44276693 | C | T | 4 | a0001c0003t0004g0296 a0001c0003t0004g0297 a0001c0003t0004g0298 others(1): Show |
4 | HG02451.hp2 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+728C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276693 | |||||||
| chr2:44276990 | G | T | 8 | a0002c0001t0001g0268 a0002c0001t0001g0269 a0002c0001t0001g0270 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+1025G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276990 | |||||||
| chr2:44276995 | G | C | 7 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(4): Show |
7 | HG02717.hp2 HG03453.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+1030G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276995 | |||||||
| chr2:44277030 | C | A | 2 | a0001c0003t0003g0277 a0001c0003t0003g0321 |
2 | HG00738.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.430+1065C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277030 | |||||||
| chr2:44277037 | C | A | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+1072C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277037 | |||||||
| chr2:44277092 | T | TTCTC | 189 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0009 others(186): Show |
205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.430+1133_430+1136d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44277092 | ||||||
| chr2:44277097 | T | G | 4 | a0001c0003t0001g0007 a0001c0003t0001g0027 a0001c0003t0001g0028 others(1): Show |
5 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+1132T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277097 | |||||||
| chr2:44277100 | C | T | 1 | a0001c0002t0003g0017 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.430+1135C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277100 | |||||||
| chr2:44277101 | T | TC | 13 | a0001c0003t0001g0294 a0001c0003t0004g0296 a0001c0003t0004g0297 others(10): Show |
13 | HG00099.hp1 HG01884.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.430+1136_430+1137i others(3): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277101 | |||||||
| chr2:44277103 | C | CT | 29 | a0001c0002t0002g0003 a0001c0002t0002g0261 a0001c0002t0002g0262 others(26): Show |
34 | HG00438.hp2 HG00639.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.430+1159dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44277103 | ||||||
| chr2:44277103 | CT | C | 34 | a0001c0002t0002g0160 a0001c0003t0001g0006 a0001c0003t0001g0295 others(31): Show |
37 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.430+1159delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44277103 | ||||||
| chr2:44277104 | T | TTC | 12 | a0001c0003t0001g0294 a0001c0003t0004g0297 a0001c0003t0004g0298 others(9): Show |
12 | HG00099.hp1 HG01884.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+1140_430+1141i others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44277104 | ||||||
| chr2:44277220 | G | A | 1 | a0002c0001t0001g0020 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.430+1255G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277220 | |||||||
| chr2:44277326 | C | T | 12 | a0001c0003t0001g0248 a0001c0003t0001g0249 a0001c0003t0001g0250 others(9): Show |
12 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+1361C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277326 | |||||||
| chr2:44277356 | C | A | 11 | a0001c0003t0001g0006 a0001c0003t0004g0278 a0001c0003t0004g0279 others(8): Show |
13 | HG01106.hp2 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.430+1391C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277356 | |||||||
| chr2:44277397 | C | T | 1 | a0002c0001t0001g0024 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.430+1432C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277397 | |||||||
| chr2:44277419 | G | A | 12 | a0001c0003t0001g0248 a0001c0003t0001g0249 a0001c0003t0001g0250 others(9): Show |
12 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+1454G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277419 | |||||||
| chr2:44277448 | A | G | 2 | a0001c0003t0003g0277 a0001c0003t0003g0321 |
2 | HG00738.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.430+1483A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277448 | |||||||
| chr2:44277449 | T | G | 1 | a0001c0017t0007g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.430+1484T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277449 | |||||||
| chr2:44277452 | A | G | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.430+1487A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277452 | |||||||
| chr2:44277532 | C | T | 1 | a0001c0017t0007g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.430+1567C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277532 | |||||||
| chr2:44277666 | G | T | 1 | a0002c0001t0001g0141 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.430+1701G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277666 | |||||||
| chr2:44277718 | C | T | 28 | a0001c0003t0002g0019 a0001c0003t0002g0119 a0001c0003t0011g0118 others(25): Show |
28 | HG00597.hp2 HG01167.hp1 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.430+1753C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277718 | |||||||
| chr2:44277738 | T | C | 210 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(207): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.430+1773T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277738 | |||||||
| chr2:44277906 | A | G | 4 | a0001c0003t0001g0007 a0001c0003t0001g0027 a0001c0003t0001g0028 others(1): Show |
5 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+1941A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277906 | |||||||
| chr2:44277925 | A | C | 1 | a0002c0001t0001g0117 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.430+1960A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277925 | |||||||
| chr2:44277949 | T | C | 1 | a0001c0002t0002g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.430+1984T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277949 | |||||||
| chr2:44278010 | C | A | 1 | a0001c0003t0001g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.430+2045C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278010 | |||||||
| chr2:44278045 | T | A | 1 | a0001c0003t0003g0301 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.430+2080T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278045 | |||||||
| chr2:44278046 | T | G | 235 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(232): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.430+2081T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278046 | |||||||
| chr2:44278182 | C | T | 6 | a0001c0003t0003g0111 a0002c0001t0001g0112 a0002c0001t0001g0113 others(3): Show |
6 | HG00280.hp1 HG01256.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+2217C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278182 | |||||||
| chr2:44278190 | A | G | 3 | a0001c0003t0001g0254 a0001c0003t0001g0255 a0001c0003t0001g0256 |
3 | HG02257.hp1 HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.430+2225A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278190 | |||||||
| chr2:44278318 | G | C | 1 | a0001c0003t0002g0019 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.430+2353G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278318 | |||||||
| chr2:44278371 | C | A | 1 | a0001c0017t0007g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.431-2345C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278371 | |||||||
| chr2:44278396 | T | G | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.431-2320T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278396 | |||||||
| chr2:44278435 | G | A | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.431-2281G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278435 | |||||||
| chr2:44278469 | T | TAAATA | 2 | a0002c0001t0001g0018 a0002c0001t0001g0302 |
3 | HG00642.hp2 HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.431-2229_431-2225d others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44278469 | ||||||
| chr2:44278582 | C | T | 1 | a0001c0003t0003g0284 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.431-2134C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278582 | |||||||
| chr2:44278740 | G | A | 7 | a0001c0003t0001g0248 a0001c0003t0001g0249 a0001c0003t0001g0254 others(4): Show |
7 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-1976G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278740 | |||||||
| chr2:44278764 | G | A | 1 | a0001c0002t0002g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.431-1952G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278764 | |||||||
| chr2:44278950 | T | C | 5 | a0001c0002t0001g0180 a0001c0002t0001g0181 a0001c0002t0002g0012 others(2): Show |
6 | HG01074.hp1 HG01099.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-1766T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278950 | |||||||
| chr2:44279006 | T | A | 38 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0027 others(35): Show |
41 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.431-1710T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279006 | |||||||
| chr2:44279008 | T | C | 1 | a0002c0001t0001g0032 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.431-1708T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279008 | |||||||
| chr2:44279117 | G | A | 24 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(21): Show |
24 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.431-1599G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279117 | |||||||
| chr2:44279206 | G | A | 154 | a0001c0003t0001g0006 a0001c0003t0001g0009 a0001c0003t0001g0010 others(151): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.431-1510G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279206 | |||||||
| chr2:44279229 | A | T | 11 | a0001c0003t0001g0006 a0001c0003t0004g0278 a0001c0003t0004g0279 others(8): Show |
13 | HG01106.hp2 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.431-1487A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279229 | |||||||
| chr2:44279374 | C | T | 1 | a0001c0002t0002g0247 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.431-1342C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279374 | |||||||
| chr2:44279429 | G | T | 1 | a0002c0001t0001g0110 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.431-1287G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279429 | |||||||
| chr2:44279485 | G | A | 1 | a0001c0003t0003g0284 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.431-1231G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279485 | |||||||
| chr2:44279567 | C | T | 1 | a0002c0001t0001g0154 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.431-1149C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279567 | |||||||
| chr2:44279588 | G | A | 1 | a0002c0001t0001g0033 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.431-1128G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279588 | |||||||
| chr2:44279601 | T | C | 26 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(23): Show |
26 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.431-1115T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279601 | |||||||
| chr2:44279610 | T | G | 6 | a0001c0003t0001g0007 a0001c0003t0001g0027 a0001c0003t0001g0028 others(3): Show |
7 | HG01243.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-1106T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279610 | |||||||
| chr2:44279782 | C | T | 155 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0009 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.431-934C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279782 | |||||||
| chr2:44279832 | G | C | 155 | a0001c0003t0001g0006 a0001c0003t0001g0009 a0001c0003t0001g0010 others(152): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.431-884G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279832 | |||||||
| chr2:44279935 | G | A | 1 | a0001c0003t0001g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.431-781G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279935 | |||||||
| chr2:44280074 | C | T | 142 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0011 others(139): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.431-642C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280074 | |||||||
| chr2:44280214 | T | G | 1 | a0001c0002t0002g0182 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.431-502T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280214 | |||||||
| chr2:44280428 | G | A | 1 | a0002c0001t0001g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.431-288G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280428 | |||||||
| chr2:44280459 | G | A | 3 | a0001c0003t0001g0009 a0001c0003t0001g0035 a0001c0003t0001g0142 |
4 | HG02647.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-257G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280459 | |||||||
| chr2:44280534 | G | A | 138 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0011 others(135): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.431-182G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280534 | |||||||
| chr2:44280608 | A | G | 1 | a0001c0003t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.431-108A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280608 | |||||||
| chr2:44280654 | A | AT | 4 | a0002c0001t0001g0025 a0002c0001t0001g0026 a0002c0001t0001g0104 others(1): Show |
4 | HG02970.hp2 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-56dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44280654 | ||||||
| chr2:44280670 | C | A | 1 | a0001c0003t0011g0118 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.431-46C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280670 | |||||||
| chr2:44280956 | T | C | 6 | a0001c0003t0003g0021 a0001c0018t0003g0159 a0002c0001t0001g0020 others(3): Show |
6 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.610+61T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | chr2 | 44280956 | |||||||
| chr2:44280990 | A | G | 1 | a0002c0001t0001g0140 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.610+95A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | chr2 | 44280990 | |||||||
| chr2:44281003 | T | TTCCC | 49 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(46): Show |
54 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.610+122_610+125dup others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 44281003 | ||||||
| chr2:44281042 | C | T | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.610+147C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | chr2 | 44281042 | |||||||
| chr2:44281054 | T | G | 19 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0010 others(16): Show |
23 | HG00642.hp1 HG01099.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.610+159T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | chr2 | 44281054 | |||||||
| chr2:44281061 | C | T | 2 | a0001c0003t0002g0103 a0002c0001t0001g0102 |
2 | NA18965.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.610+166C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | chr2 | 44281061 | |||||||
| chr2:44281064 | C | G | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.610+169C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | chr2 | 44281064 | |||||||
| chr2:44281159 | C | CT | 197 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(194): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.611-212dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 44281159 | ||||||
| chr2:44281159 | C | CTT | 13 | a0001c0003t0002g0101 a0001c0003t0003g0021 a0001c0003t0003g0277 others(10): Show |
13 | HG00738.hp1 HG02074.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.611-213_611-212dup others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 44281159 | ||||||
| chr2:44281377 | T | TACTCATT others(228): Show |
1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.611-7_765+73dupTCA others(232): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 44281377 | ||||||
| chr2:44281696 | G | A | 174 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0010 others(171): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.765+155G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44281696 | |||||||
| chr2:44281812 | C | T | 1 | a0001c0002t0002g0243 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.765+271C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44281812 | |||||||
| chr2:44281826 | TTCCATG | T | 7 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0027 others(4): Show |
10 | HG01106.hp2 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.765+289_765+294del others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 44281826 | ||||||
| chr2:44282016 | C | T | 1 | a0001c0002t0002g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.765+475C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282016 | |||||||
| chr2:44282021 | G | A | 1 | a0002c0001t0001g0141 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.765+480G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282021 | |||||||
| chr2:44282185 | T | A | 1 | a0001c0002t0002g0183 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.765+644T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282185 | |||||||
| chr2:44282216 | C | G | 1 | a0001c0003t0003g0277 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.765+675C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282216 | |||||||
| chr2:44282223 | T | C | 2 | a0001c0003t0001g0294 a0001c0003t0001g0295 |
2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.765+682T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282223 | |||||||
| chr2:44282248 | T | C | 1 | a0002c0001t0001g0155 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.765+707T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282248 | |||||||
| chr2:44282425 | C | A | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.765+884C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282425 | |||||||
| chr2:44282432 | G | A | 3 | a0002c0001t0001g0025 a0002c0001t0001g0026 a0002c0001t0001g0104 |
3 | HG02970.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.765+891G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282432 | |||||||
| chr2:44282510 | G | T | 1 | a0002c0001t0001g0155 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.765+969G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282510 | |||||||
| chr2:44282514 | C | G | 1 | a0001c0003t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.765+973C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282514 | |||||||
| chr2:44282623 | C | T | 1 | a0002c0010t0001g0099 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.765+1082C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282623 | |||||||
| chr2:44282639 | T | A | 1 | a0002c0001t0001g0155 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.765+1098T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282639 | |||||||
| chr2:44282744 | G | A | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.765+1203G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282744 | |||||||
| chr2:44282902 | C | T | 1 | a0001c0003t0006g0285 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.765+1361C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282902 | |||||||
| chr2:44282921 | G | C | 1 | a0002c0001t0001g0051 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.765+1380G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282921 | |||||||
| chr2:44283007 | A | T | 189 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(186): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.765+1466A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283007 | |||||||
| chr2:44283040 | T | C | 214 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(211): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.765+1499T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283040 | |||||||
| chr2:44283057 | G | T | 25 | a0001c0003t0003g0021 a0001c0003t0004g0016 a0001c0003t0004g0276 others(22): Show |
25 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.765+1516G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283057 | |||||||
| chr2:44283268 | G | A | 1 | a0001c0003t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.765+1727G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283268 | |||||||
| chr2:44283335 | C | G | 1 | a0001c0002t0002g0265 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.765+1794C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283335 | |||||||
| chr2:44283439 | C | T | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.765+1898C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283439 | |||||||
| chr2:44283650 | A | T | 1 | a0002c0001t0001g0155 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.765+2109A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283650 | |||||||
| chr2:44283722 | C | A | 1 | a0002c0001t0001g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.765+2181C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283722 | |||||||
| chr2:44283797 | C | T | 16 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(13): Show |
16 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.766-2235C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283797 | |||||||
| chr2:44283839 | T | C | 1 | a0002c0001t0001g0155 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.766-2193T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283839 | |||||||
| chr2:44283858 | T | TAGGTATA others(313): Show |
11 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.766-2159_766-2158i others(322): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 44283858 | ||||||
| chr2:44284016 | T | A | 1 | a0001c0003t0001g0036 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.766-2016T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284016 | |||||||
| chr2:44284076 | C | T | 1 | a0001c0002t0009g0176 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.766-1956C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284076 | |||||||
| chr2:44284118 | C | T | 1 | a0001c0003t0002g0019 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.766-1914C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284118 | |||||||
| chr2:44284297 | C | A | 1 | a0002c0001t0001g0110 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.766-1735C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284297 | |||||||
| chr2:44284528 | A | T | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.766-1504A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284528 | |||||||
| chr2:44284648 | G | T | 3 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0253 |
3 | HG03130.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.766-1384G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284648 | |||||||
| chr2:44284667 | A | G | 13 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0011 others(10): Show |
16 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.766-1365A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284667 | |||||||
| chr2:44284722 | T | C | 214 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(211): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.766-1310T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284722 | |||||||
| chr2:44284790 | T | C | 178 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(175): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.766-1242T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284790 | |||||||
| chr2:44284897 | A | C | 1 | a0001c0003t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.766-1135A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284897 | |||||||
| chr2:44285149 | C | T | 1 | a0002c0001t0001g0098 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.766-883C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285149 | |||||||
| chr2:44285402 | G | A | 1 | a0001c0003t0012g0292 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.766-630G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285402 | |||||||
| chr2:44285440 | C | T | 3 | a0001c0003t0003g0277 a0001c0003t0003g0284 a0001c0003t0003g0321 |
3 | HG00738.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.766-592C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285440 | |||||||
| chr2:44285696 | C | G | 1 | a0001c0002t0002g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.766-336C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285696 | |||||||
| chr2:44285813 | G | A | 4 | a0001c0002t0002g0185 a0001c0002t0002g0186 a0001c0002t0002g0187 others(1): Show |
4 | HG01081.hp1 HG01106.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-219G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285813 | |||||||
| chr2:44285831 | C | T | 2 | a0001c0002t0002g0239 a0001c0002t0002g0240 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.766-201C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285831 | |||||||
| chr2:44285832 | G | A | 211 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(208): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.766-200G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285832 | |||||||
| chr2:44285948 | G | A | 2 | a0001c0003t0012g0292 a0001c0003t0013g0293 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.766-84G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285948 | |||||||
| chr2:44285953 | G | T | 1 | a0001c0002t0002g0238 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.766-79G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285953 | |||||||
| chr2:44285996 | A | G | 3 | a0001c0003t0001g0009 a0001c0003t0001g0035 a0001c0003t0001g0142 |
4 | HG02647.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-36A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285996 | |||||||
| chr2:44286497 | ACGGTGCC others(17): Show |
A | 5 | a0001c0002t0002g0236 a0001c0003t0001g0006 a0001c0003t0001g0150 others(2): Show |
7 | HG01106.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.891+418_891+441del others(24): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286497 | ||||||
| chr2:44286497 | ACGGTGCC others(41): Show |
A | 155 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(152): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.891+394_891+441del others(48): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286497 | ||||||
| chr2:44286536 | GTGAGCTG others(87): Show |
G | 1 | a0002c0001t0001g0052 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.891+390_891+483del others(94): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286536 | ||||||
| chr2:44286551 | C | T | 4 | a0002c0001t0001g0018 a0002c0001t0001g0143 a0002c0001t0001g0302 others(1): Show |
5 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+394C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286551 | |||||||
| chr2:44286551 | CCTGTGAC others(41): Show |
C | 4 | a0001c0003t0004g0016 a0001c0003t0004g0276 a0001c0003t0004g0290 others(1): Show |
4 | HG02109.hp1 HG02451.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+418_891+465del others(48): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286551 | ||||||
| chr2:44286575 | C | T | 15 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(12): Show |
16 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+418C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286575 | |||||||
| chr2:44286575 | CCTGTGAC others(17): Show |
C | 5 | a0001c0003t0004g0053 a0001c0003t0004g0287 a0001c0003t0004g0288 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+450_891+473del others(24): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286575 | ||||||
| chr2:44286575 | CCTGTGAC others(63): Show |
C | 1 | a0001c0003t0011g0118 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.891+466_891+535del others(70): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286575 | ||||||
| chr2:44286582 | CGG | C | 3 | a0002c0001t0001g0018 a0002c0001t0001g0302 a0002c0001t0010g0316 |
4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+426_891+427del others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286582 | |||||||
| chr2:44286584 | GTGAGCTG others(39): Show |
G | 1 | a0002c0001t0001g0143 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.891+438_891+483del others(46): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286584 | ||||||
| chr2:44286591 | G | GTGCGGTG others(129): Show |
7 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+449_891+450ins others(136): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286591 | ||||||
| chr2:44286595 | G | A | 3 | a0002c0001t0001g0018 a0002c0001t0001g0302 a0002c0001t0010g0316 |
4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+438G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286595 | |||||||
| chr2:44286596 | G | C | 3 | a0002c0001t0001g0018 a0002c0001t0001g0302 a0002c0001t0010g0316 |
4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+439G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286596 | |||||||
| chr2:44286596 | G | GTGTCTGT others(15): Show |
4 | a0001c0003t0004g0281 a0001c0003t0004g0282 a0001c0003t0004g0283 others(1): Show |
4 | HG01891.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+449_891+450ins others(22): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286596 | ||||||
| chr2:44286620 | GTGTCTGT others(15): Show |
G | 3 | a0002c0001t0001g0018 a0002c0001t0001g0302 a0002c0001t0010g0316 |
4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+474_891+495del others(22): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286620 | ||||||
| chr2:44286623 | T | C | 7 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+466T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286623 | |||||||
| chr2:44286630 | C | CGG | 7 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+473_891+474ins others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286630 | |||||||
| chr2:44286630 | C | CGGTGAGC others(109): Show |
4 | a0001c0003t0004g0281 a0001c0003t0004g0282 a0001c0003t0004g0283 others(1): Show |
4 | HG01891.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+473_891+474ins others(116): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286630 | |||||||
| chr2:44286641 | A | G | 11 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+484A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286641 | |||||||
| chr2:44286642 | C | G | 11 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+485C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286642 | |||||||
| chr2:44286645 | T | C | 11 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+488T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286645 | |||||||
| chr2:44286665 | G | A | 1 | a0002c0001t0001g0054 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.891+508G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286665 | |||||||
| chr2:44286669 | T | C | 3 | a0002c0001t0001g0018 a0002c0001t0001g0302 a0002c0001t0010g0316 |
4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+512T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286669 | |||||||
| chr2:44286676 | CGG | C | 3 | a0002c0001t0001g0018 a0002c0001t0001g0302 a0002c0001t0010g0316 |
4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+520_891+521del others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286676 | |||||||
| chr2:44286693 | C | T | 3 | a0002c0001t0001g0018 a0002c0001t0001g0302 a0002c0001t0010g0316 |
4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+536C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286693 | |||||||
| chr2:44286711 | G | A | 3 | a0002c0001t0001g0018 a0002c0001t0001g0302 a0002c0001t0010g0316 |
4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+554G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286711 | |||||||
| chr2:44286715 | T | C | 3 | a0002c0001t0001g0018 a0002c0001t0001g0302 a0002c0001t0010g0316 |
4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+558T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286715 | |||||||
| chr2:44286733 | A | G | 14 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(11): Show |
15 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.891+576A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286733 | |||||||
| chr2:44286737 | C | T | 3 | a0002c0001t0001g0018 a0002c0001t0001g0302 a0002c0001t0010g0316 |
4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+580C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286737 | |||||||
| chr2:44286744 | C | CGG | 3 | a0002c0001t0001g0018 a0002c0001t0001g0302 a0002c0001t0010g0316 |
4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+587_891+588ins others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286744 | |||||||
| chr2:44286759 | T | C | 3 | a0002c0001t0001g0018 a0002c0001t0001g0302 a0002c0001t0010g0316 |
4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+602T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286759 | |||||||
| chr2:44286838 | T | C | 1 | a0001c0002t0002g0189 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.891+681T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286838 | |||||||
| chr2:44286937 | T | G | 1 | a0002c0001t0001g0144 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.891+780T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286937 | |||||||
| chr2:44287071 | T | C | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.891+914T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287071 | |||||||
| chr2:44287132 | C | G | 3 | a0001c0003t0001g0009 a0001c0003t0001g0035 a0001c0003t0001g0142 |
4 | HG02647.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+975C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287132 | |||||||
| chr2:44287299 | T | C | 13 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0011 others(10): Show |
16 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+1142T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287299 | |||||||
| chr2:44287364 | G | A | 2 | a0001c0002t0002g0190 a0001c0002t0002g0191 |
2 | NA19011.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.891+1207G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287364 | |||||||
| chr2:44287395 | G | A | 7 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0027 others(4): Show |
10 | HG01106.hp2 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+1238G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287395 | |||||||
| chr2:44287548 | G | T | 1 | a0002c0001t0001g0098 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.891+1391G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287548 | |||||||
| chr2:44287758 | G | A | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+1601G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287758 | |||||||
| chr2:44287896 | C | G | 1 | a0001c0003t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.891+1739C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287896 | |||||||
| chr2:44287929 | A | G | 10 | a0001c0002t0002g0164 a0001c0003t0004g0016 a0001c0003t0004g0053 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+1772A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287929 | |||||||
| chr2:44287945 | C | T | 23 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(20): Show |
23 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.891+1788C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287945 | |||||||
| chr2:44287946 | A | G | 5 | a0001c0003t0006g0266 a0001c0003t0006g0285 a0001c0003t0012g0292 others(2): Show |
5 | HG01884.hp1 HG02886.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+1789A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287946 | |||||||
| chr2:44288032 | CT | C | 12 | a0001c0002t0002g0164 a0001c0003t0001g0035 a0001c0003t0004g0016 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.891+1890delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44288032 | ||||||
| chr2:44288118 | C | T | 88 | a0001c0003t0002g0084 a0001c0003t0002g0103 a0001c0003t0002g0109 others(85): Show |
98 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.891+1961C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288118 | |||||||
| chr2:44288241 | G | C | 1 | a0001c0003t0003g0320 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.891+2084G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288241 | |||||||
| chr2:44288399 | C | T | 3 | a0001c0003t0003g0277 a0001c0003t0003g0284 a0001c0003t0003g0321 |
3 | HG00738.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.891+2242C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288399 | |||||||
| chr2:44288440 | C | T | 3 | a0002c0001t0001g0143 a0002c0001t0001g0145 a0002c0001t0001g0146 |
3 | HG03017.hp1 HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.891+2283C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288440 | |||||||
| chr2:44288472 | T | C | 1 | a0001c0003t0001g0010 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.891+2315T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288472 | |||||||
| chr2:44288517 | T | A | 3 | a0001c0003t0003g0277 a0001c0003t0003g0284 a0001c0003t0003g0321 |
3 | HG00738.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.891+2360T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288517 | |||||||
| chr2:44288529 | C | T | 23 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(20): Show |
23 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.891+2372C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288529 | |||||||
| chr2:44288680 | A | G | 1 | a0001c0002t0002g0235 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.891+2523A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288680 | |||||||
| chr2:44288712 | C | T | 8 | a0002c0001t0001g0268 a0002c0001t0001g0269 a0002c0001t0001g0270 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.891+2555C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288712 | |||||||
| chr2:44288861 | G | T | 1 | a0001c0002t0002g0234 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.891+2704G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288861 | |||||||
| chr2:44288948 | C | A | 21 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0011 others(18): Show |
24 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.891+2791C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288948 | |||||||
| chr2:44288949 | C | A | 21 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0011 others(18): Show |
24 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.891+2792C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288949 | |||||||
| chr2:44289021 | GAT | G | 4 | a0001c0003t0006g0285 a0001c0003t0012g0292 a0001c0003t0013g0293 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+2865_891+2866d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289021 | |||||||
| chr2:44289143 | A | G | 221 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(218): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.891+2986A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289143 | |||||||
| chr2:44289217 | CT | C | 7 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0027 others(4): Show |
10 | HG01106.hp2 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+3071delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44289217 | ||||||
| chr2:44289334 | C | A | 1 | a0002c0001t0001g0141 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.891+3177C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289334 | |||||||
| chr2:44289436 | C | T | 1 | a0001c0003t0001g0042 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.891+3279C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289436 | |||||||
| chr2:44289492 | T | C | 9 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(6): Show |
10 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+3335T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289492 | |||||||
| chr2:44289627 | CTATT | C | 11 | a0001c0002t0002g0164 a0001c0003t0004g0016 a0001c0003t0004g0053 others(8): Show |
11 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+3480_891+3483d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44289627 | ||||||
| chr2:44289629 | A | G | 7 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0027 others(4): Show |
10 | HG01106.hp2 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+3472A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289629 | |||||||
| chr2:44289753 | C | A | 13 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0011 others(10): Show |
16 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+3596C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289753 | |||||||
| chr2:44289777 | C | T | 2 | a0002c0001t0001g0096 a0002c0001t0001g0097 |
2 | HG01069.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.891+3620C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289777 | |||||||
| chr2:44289808 | T | G | 1 | a0001c0002t0002g0013 | 2 | NA18965.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.891+3651T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289808 | |||||||
| chr2:44289822 | C | T | 1 | a0002c0001t0001g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.891+3665C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289822 | |||||||
| chr2:44289858 | T | G | 1 | a0001c0002t0002g0192 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.891+3701T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289858 | |||||||
| chr2:44289895 | T | A | 1 | a0002c0001t0001g0066 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.891+3738T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289895 | |||||||
| chr2:44289897 | C | G | 1 | a0002c0001t0001g0066 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.891+3740C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289897 | |||||||
| chr2:44289933 | A | C | 173 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(170): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.891+3776A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289933 | |||||||
| chr2:44289941 | A | AT | 16 | a0001c0002t0003g0233 a0001c0003t0001g0150 a0001c0003t0003g0300 others(13): Show |
16 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+3791dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44289941 | ||||||
| chr2:44290009 | A | G | 25 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(22): Show |
25 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.891+3852A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290009 | |||||||
| chr2:44290051 | T | A | 20 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0011 others(17): Show |
23 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.891+3894T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290051 | |||||||
| chr2:44290115 | C | T | 2 | a0002c0001t0001g0137 a0002c0001t0001g0138 |
2 | HG02523.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.891+3958C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290115 | |||||||
| chr2:44290123 | C | CT | 162 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(159): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.891+3983dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44290123 | ||||||
| chr2:44290123 | C | CTT | 14 | a0001c0002t0001g0175 a0001c0003t0001g0251 a0001c0003t0004g0297 others(11): Show |
14 | HG01069.hp2 HG01071.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.891+3982_891+3983d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44290123 | ||||||
| chr2:44290123 | CT | C | 31 | a0001c0002t0002g0164 a0001c0002t0002g0194 a0001c0003t0001g0009 others(28): Show |
34 | HG00621.hp2 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.891+3983delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44290123 | ||||||
| chr2:44290337 | T | G | 11 | a0001c0002t0002g0164 a0001c0003t0004g0016 a0001c0003t0004g0053 others(8): Show |
11 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+4180T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290337 | |||||||
| chr2:44290420 | G | A | 2 | a0001c0003t0003g0277 a0001c0003t0003g0321 |
2 | HG00738.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.891+4263G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290420 | |||||||
| chr2:44290523 | T | C | 172 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(169): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.891+4366T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290523 | |||||||
| chr2:44290583 | G | A | 6 | a0001c0003t0001g0007 a0001c0003t0001g0027 a0001c0003t0001g0028 others(3): Show |
7 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.891+4426G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290583 | |||||||
| chr2:44290613 | G | A | 161 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(158): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.891+4456G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290613 | |||||||
| chr2:44290620 | T | C | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+4463T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290620 | |||||||
| chr2:44290683 | C | CT | 212 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(209): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.891+4539dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44290683 | ||||||
| chr2:44290683 | C | CTT | 15 | a0001c0002t0001g0175 a0001c0003t0003g0277 a0001c0003t0003g0321 others(12): Show |
15 | HG00738.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.891+4538_891+4539d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44290683 | ||||||
| chr2:44290700 | G | A | 215 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(212): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.891+4543G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290700 | |||||||
| chr2:44291199 | G | C | 11 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+5042G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291199 | |||||||
| chr2:44291420 | G | A | 17 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(14): Show |
17 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.891+5263G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291420 | |||||||
| chr2:44291438 | A | T | 1 | a0001c0002t0002g0231 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.891+5281A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291438 | |||||||
| chr2:44291439 | T | C | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.891+5282T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291439 | |||||||
| chr2:44291495 | C | G | 1 | a0002c0001t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.891+5338C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291495 | |||||||
| chr2:44291613 | G | T | 8 | a0001c0003t0003g0315 a0002c0001t0001g0033 a0002c0001t0001g0085 others(5): Show |
8 | HG00280.hp2 HG02280.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.891+5456G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291613 | |||||||
| chr2:44291647 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.891+5490C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291647 | |||||||
| chr2:44291661 | G | T | 1 | a0002c0001t0001g0117 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.891+5504G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291661 | |||||||
| chr2:44291719 | G | A | 1 | a0001c0003t0003g0301 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.891+5562G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291719 | |||||||
| chr2:44291910 | G | A | 7 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0027 others(4): Show |
10 | HG01106.hp2 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+5753G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291910 | |||||||
| chr2:44291934 | T | C | 1 | a0001c0003t0003g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.891+5777T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291934 | |||||||
| chr2:44292003 | A | G | 187 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(184): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.891+5846A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292003 | |||||||
| chr2:44292151 | C | T | 11 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(8): Show |
11 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+5994C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292151 | |||||||
| chr2:44292174 | C | G | 1 | a0001c0003t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.891+6017C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292174 | |||||||
| chr2:44292205 | A | C | 1 | a0001c0003t0004g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.891+6048A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292205 | |||||||
| chr2:44292392 | C | T | 1 | a0001c0002t0002g0230 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.891+6235C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292392 | |||||||
| chr2:44292405 | C | G | 13 | a0001c0003t0001g0009 a0001c0003t0001g0010 a0001c0003t0001g0011 others(10): Show |
16 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+6248C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292405 | |||||||
| chr2:44292424 | A | C | 1 | a0001c0002t0002g0229 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.891+6267A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292424 | |||||||
| chr2:44292475 | G | T | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.891+6318G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292475 | |||||||
| chr2:44292526 | G | C | 1 | a0001c0002t0003g0233 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.891+6369G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292526 | |||||||
| chr2:44292551 | C | T | 1 | a0002c0004t0001g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.891+6394C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292551 | |||||||
| chr2:44292574 | C | T | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+6417C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292574 | |||||||
| chr2:44292630 | T | C | 3 | a0002c0001t0001g0143 a0002c0001t0001g0145 a0002c0001t0001g0146 |
3 | HG03017.hp1 HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.891+6473T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292630 | |||||||
| chr2:44292766 | GATAT | G | 10 | a0001c0002t0002g0164 a0001c0003t0004g0016 a0001c0003t0004g0053 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+6613_891+6616d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44292766 | ||||||
| chr2:44293146 | G | C | 1 | a0002c0016t0001g0161 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.892-6825G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293146 | |||||||
| chr2:44293362 | C | G | 1 | a0002c0001t0001g0273 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.892-6609C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293362 | |||||||
| chr2:44293444 | G | A | 1 | a0001c0003t0003g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.892-6527G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293444 | |||||||
| chr2:44293517 | AG | A | 166 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(163): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.892-6448delG | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44293517 | ||||||
| chr2:44293523 | G | A | 54 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(51): Show |
59 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.892-6448G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293523 | |||||||
| chr2:44293523 | GA | G | 3 | a0001c0003t0001g0006 a0001c0003t0002g0258 a0009c0015t0001g0252 |
5 | HG01106.hp2 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-6438delA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44293523 | ||||||
| chr2:44293525 | A | G | 1 | a0001c0002t0002g0264 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.892-6446A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293525 | |||||||
| chr2:44293547 | G | A | 1 | a0002c0001t0001g0317 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.892-6424G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293547 | |||||||
| chr2:44293577 | A | G | 198 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(195): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.892-6394A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293577 | |||||||
| chr2:44293764 | G | C | 1 | a0001c0003t0001g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.892-6207G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293764 | |||||||
| chr2:44293870 | C | G | 1 | a0002c0001t0001g0136 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.892-6101C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293870 | |||||||
| chr2:44293959 | T | TG | 230 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(227): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.892-6012_892-6011i others(3): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293959 | |||||||
| chr2:44294037 | C | T | 2 | a0001c0002t0002g0239 a0001c0002t0002g0240 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.892-5934C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44294037 | |||||||
| chr2:44294107 | A | G | 230 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(227): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.892-5864A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44294107 | |||||||
| chr2:44294405 | T | C | 225 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(222): Show |
243 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.892-5566T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44294405 | |||||||
| chr2:44294469 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.892-5502C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44294469 | |||||||
| chr2:44294502 | CA | C | 14 | a0001c0002t0002g0194 a0001c0002t0002g0226 a0001c0002t0002g0227 others(11): Show |
14 | HG00639.hp1 HG01167.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.892-5451delA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44294502 | ||||||
| chr2:44294625 | A | G | 1 | a0002c0001t0001g0051 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.892-5346A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44294625 | |||||||
| chr2:44294959 | G | T | 3 | a0001c0002t0002g0189 a0001c0002t0002g0225 a0001c0002t0002g0229 |
3 | NA18944.hp2 NA18946.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.892-5012G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44294959 | |||||||
| chr2:44295032 | C | G | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-4939C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295032 | |||||||
| chr2:44295141 | G | A | 1 | a0002c0001t0001g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.892-4830G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295141 | |||||||
| chr2:44295186 | AACTTGCT others(12): Show |
A | 1 | a0001c0003t0003g0284 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.892-4776_892-4758d others(21): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44295186 | ||||||
| chr2:44295261 | G | A | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-4710G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295261 | |||||||
| chr2:44295421 | G | C | 1 | a0001c0002t0002g0195 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.892-4550G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295421 | |||||||
| chr2:44295485 | T | G | 1 | a0001c0003t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.892-4486T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295485 | |||||||
| chr2:44295602 | A | C | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-4369A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295602 | |||||||
| chr2:44295614 | C | T | 1 | a0002c0001t0001g0102 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.892-4357C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295614 | |||||||
| chr2:44295666 | C | T | 1 | a0001c0003t0004g0291 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.892-4305C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295666 | |||||||
| chr2:44295683 | G | A | 3 | a0001c0003t0003g0277 a0001c0003t0003g0284 a0001c0003t0003g0321 |
3 | HG00738.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.892-4288G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295683 | |||||||
| chr2:44295689 | T | C | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-4282T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295689 | |||||||
| chr2:44295877 | CTT | C | 3 | a0002c0001t0001g0120 a0002c0001t0001g0121 a0002c0001t0001g0158 |
3 | NA18948.hp1 NA18967.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.892-4091_892-4090d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44295877 | ||||||
| chr2:44295920 | G | A | 1 | a0001c0003t0003g0304 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.892-4051G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295920 | |||||||
| chr2:44296497 | A | G | 3 | a0002c0001t0001g0106 a0002c0001t0001g0107 a0002c0001t0001g0108 |
3 | NA18999.hp2 NA19057.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.892-3474A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296497 | |||||||
| chr2:44296769 | A | T | 2 | a0001c0002t0002g0188 a0002c0001t0001g0066 |
2 | HG01106.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.892-3202A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296769 | |||||||
| chr2:44296789 | C | T | 1 | a0001c0003t0004g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.892-3182C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296789 | |||||||
| chr2:44296832 | G | T | 1 | a0001c0002t0002g0224 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.892-3139G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296832 | |||||||
| chr2:44296922 | C | T | 1 | a0001c0003t0004g0288 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.892-3049C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296922 | |||||||
| chr2:44296925 | G | A | 130 | a0001c0002t0002g0188 a0001c0003t0001g0008 a0001c0003t0001g0031 others(127): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.892-3046G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296925 | |||||||
| chr2:44296951 | G | A | 1 | a0002c0001t0001g0137 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.892-3020G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296951 | |||||||
| chr2:44296953 | C | T | 1 | a0001c0003t0003g0311 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.892-3018C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296953 | |||||||
| chr2:44297040 | C | A | 1 | a0002c0001t0001g0089 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.892-2931C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297040 | |||||||
| chr2:44297130 | G | A | 1 | a0004c0006t0001g0045 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.892-2841G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297130 | |||||||
| chr2:44297244 | C | T | 1 | a0001c0002t0002g0235 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.892-2727C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297244 | |||||||
| chr2:44297436 | T | C | 167 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(164): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.892-2535T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297436 | |||||||
| chr2:44297491 | T | A | 10 | a0001c0002t0002g0164 a0001c0003t0004g0016 a0001c0003t0004g0053 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.892-2480T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297491 | |||||||
| chr2:44297513 | T | G | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-2458T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297513 | |||||||
| chr2:44297626 | C | T | 5 | a0001c0002t0009g0176 a0001c0003t0006g0266 a0001c0003t0006g0285 others(2): Show |
5 | HG02886.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-2345C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297626 | |||||||
| chr2:44297636 | G | A | 1 | a0002c0001t0001g0154 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.892-2335G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297636 | |||||||
| chr2:44297637 | G | A | 1 | a0002c0001t0001g0154 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.892-2334G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297637 | |||||||
| chr2:44297652 | C | T | 1 | a0001c0002t0002g0223 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.892-2319C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297652 | |||||||
| chr2:44297723 | G | A | 1 | a0002c0001t0001g0144 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.892-2248G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297723 | |||||||
| chr2:44297758 | C | T | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-2213C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297758 | |||||||
| chr2:44297760 | C | A | 2 | a0001c0003t0001g0008 a0001c0003t0001g0031 |
3 | HG01346.hp1 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.892-2211C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297760 | |||||||
| chr2:44297797 | T | A | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-2174T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297797 | |||||||
| chr2:44297806 | C | T | 8 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(5): Show |
9 | HG00280.hp1 HG00738.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.892-2165C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297806 | |||||||
| chr2:44297808 | G | A | 1 | a0001c0003t0004g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.892-2163G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297808 | |||||||
| chr2:44297842 | C | G | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-2129C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297842 | |||||||
| chr2:44297861 | T | C | 1 | a0001c0003t0003g0277 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.892-2110T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297861 | |||||||
| chr2:44298095 | T | C | 1 | a0001c0003t0001g0254 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.892-1876T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298095 | |||||||
| chr2:44298100 | G | C | 1 | a0001c0003t0003g0305 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.892-1871G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298100 | |||||||
| chr2:44298159 | AC | A | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-1811delC | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298159 | |||||||
| chr2:44298176 | C | T | 1 | a0001c0003t0003g0277 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.892-1795C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298176 | |||||||
| chr2:44298184 | C | G | 4 | a0002c0001t0001g0134 a0002c0001t0001g0151 a0002c0001t0001g0152 others(1): Show |
4 | HG02056.hp1 HG02071.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-1787C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298184 | |||||||
| chr2:44298187 | TA | T | 210 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(207): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.892-1776delA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44298187 | ||||||
| chr2:44298216 | T | C | 2 | a0001c0003t0003g0277 a0001c0003t0003g0321 |
2 | HG00738.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.892-1755T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298216 | |||||||
| chr2:44298239 | G | A | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-1732G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298239 | |||||||
| chr2:44298259 | C | G | 1 | a0001c0002t0002g0228 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.892-1712C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298259 | |||||||
| chr2:44298345 | C | T | 4 | a0002c0001t0001g0317 a0002c0001t0001g0318 a0002c0001t0010g0316 others(1): Show |
4 | HG01192.hp2 HG02698.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-1626C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298345 | |||||||
| chr2:44298370 | A | G | 3 | a0002c0001t0001g0143 a0002c0001t0001g0145 a0002c0001t0001g0146 |
3 | HG03017.hp1 HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.892-1601A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298370 | |||||||
| chr2:44298384 | C | CT | 42 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 others(39): Show |
45 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.892-1578dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44298384 | ||||||
| chr2:44298501 | C | T | 1 | a0002c0016t0001g0161 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.892-1470C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298501 | |||||||
| chr2:44298526 | T | C | 22 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(19): Show |
24 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.892-1445T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298526 | |||||||
| chr2:44298665 | G | A | 34 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(31): Show |
41 | HG00438.hp2 HG00733.hp2 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.892-1306G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298665 | |||||||
| chr2:44298871 | G | A | 169 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(166): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.892-1100G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298871 | |||||||
| chr2:44299031 | C | CT | 30 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(27): Show |
33 | HG00621.hp2 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.892-918dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44299031 | ||||||
| chr2:44299031 | CT | C | 142 | a0001c0002t0002g0178 a0001c0002t0002g0188 a0001c0002t0002g0197 others(139): Show |
154 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.892-918delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44299031 | ||||||
| chr2:44299031 | CTT | C | 21 | a0001c0003t0003g0021 a0001c0003t0003g0321 a0001c0003t0004g0296 others(18): Show |
21 | HG00099.hp1 HG00099.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.892-919_892-918del others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44299031 | ||||||
| chr2:44299031 | CTTTTTTT | C | 12 | a0001c0002t0001g0181 a0001c0002t0002g0013 a0001c0002t0002g0014 others(9): Show |
14 | HG02040.hp1 HG02040.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.892-924_892-918del others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44299031 | ||||||
| chr2:44299032 | T | C | 1 | a0001c0002t0002g0224 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.892-939T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299032 | |||||||
| chr2:44299033 | T | C | 1 | a0001c0002t0002g0209 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.892-938T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299033 | |||||||
| chr2:44299052 | TTA | T | 10 | a0001c0002t0002g0164 a0001c0003t0004g0016 a0001c0003t0004g0053 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.892-918_892-917del others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299052 | |||||||
| chr2:44299145 | T | TCACCTG | 3 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 |
3 | HG00738.hp2 HG00741.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.892-825_892-824ins others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44299145 | ||||||
| chr2:44299197 | C | T | 20 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(17): Show |
22 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.892-774C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299197 | |||||||
| chr2:44299392 | T | C | 34 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(31): Show |
41 | HG00438.hp2 HG00733.hp2 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.892-579T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299392 | |||||||
| chr2:44299405 | G | A | 5 | a0001c0003t0001g0007 a0001c0003t0001g0027 a0001c0003t0001g0028 others(2): Show |
6 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.892-566G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299405 | |||||||
| chr2:44299411 | A | G | 1 | a0002c0001t0001g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.892-560A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299411 | |||||||
| chr2:44299479 | C | A | 1 | a0001c0003t0001g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.892-492C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299479 | |||||||
| chr2:44299582 | T | C | 3 | a0001c0002t0002g0160 a0001c0002t0002g0212 a0001c0002t0002g0226 |
3 | NA18947.hp2 NA18960.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.892-389T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299582 | |||||||
| chr2:44299954 | T | G | 2 | a0001c0003t0003g0312 a0001c0003t0003g0313 |
2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.892-17T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299954 | |||||||
| chr2:44299965 | C | G | 1 | a0002c0016t0001g0161 | 1 | HG02886.hp1 | splice_region_variant&intron_variant | LOW | c.892-6C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299965 | |||||||
| chr2:44300282 | T | A | 10 | a0001c0002t0002g0164 a0001c0003t0004g0016 a0001c0003t0004g0053 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1011+192T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300282 | |||||||
| chr2:44300293 | C | T | 17 | a0001c0002t0003g0017 a0001c0002t0003g0259 a0001c0002t0003g0260 others(14): Show |
19 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1011+203C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300293 | |||||||
| chr2:44300525 | C | A | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1011+435C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300525 | |||||||
| chr2:44300562 | C | T | 1 | a0001c0003t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1012-441C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300562 | |||||||
| chr2:44300716 | A | T | 1 | a0001c0003t0001g0253 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1012-287A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300716 | |||||||
| chr2:44300960 | A | T | 1 | a0002c0001t0001g0054 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1012-43A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300960 | |||||||
| chr2:44300972 | G | A | 4 | a0001c0002t0002g0164 a0001c0003t0004g0053 a0001c0003t0004g0287 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-31G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300972 | |||||||
| chr2:44300980 | C | T | 1 | a0001c0003t0003g0284 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1012-23C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300980 | |||||||
| chr2:44301128 | GT | G | 40 | a0001c0002t0002g0164 a0001c0002t0003g0017 a0001c0002t0003g0184 others(37): Show |
42 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(39): Show |
splice_region_variant&intron_variant | LOW | c.1136+3delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44301128 | ||||||
| chr2:44301432 | T | A | 15 | a0001c0002t0001g0165 a0001c0002t0001g0175 a0001c0003t0001g0009 others(12): Show |
18 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.1136+305T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301432 | |||||||
| chr2:44301463 | G | A | 10 | a0001c0002t0002g0164 a0001c0003t0004g0016 a0001c0003t0004g0053 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1136+336G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301463 | |||||||
| chr2:44301542 | C | G | 17 | a0001c0002t0003g0233 a0001c0003t0001g0150 a0001c0003t0003g0300 others(14): Show |
17 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1136+415C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301542 | |||||||
| chr2:44301547 | T | A | 2 | a0002c0001t0005g0063 a0002c0001t0005g0064 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1136+420T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301547 | |||||||
| chr2:44301558 | G | A | 9 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(6): Show |
10 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1136+431G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301558 | |||||||
| chr2:44301693 | T | G | 1 | a0009c0015t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1136+566T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301693 | |||||||
| chr2:44301738 | C | CA | 41 | a0001c0002t0002g0164 a0001c0002t0002g0185 a0001c0003t0001g0007 others(38): Show |
42 | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1136+629dupA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44301738 | ||||||
| chr2:44301738 | C | CAA | 157 | a0001c0002t0001g0165 a0001c0002t0001g0174 a0001c0002t0001g0181 others(154): Show |
173 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1136+628_1136+629d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44301738 | ||||||
| chr2:44301738 | C | CAAA | 10 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 others(7): Show |
10 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1136+627_1136+629d others(5): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44301738 | ||||||
| chr2:44301783 | C | G | 277 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(274): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1136+656C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301783 | |||||||
| chr2:44301798 | T | C | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1136+671T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301798 | |||||||
| chr2:44301895 | A | ACT | 3 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0253 |
3 | HG03130.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1136+769_1136+770d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44301895 | ||||||
| chr2:44301978 | C | T | 1 | a0002c0001t0001g0051 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1136+851C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301978 | |||||||
| chr2:44302013 | C | G | 5 | a0001c0002t0009g0176 a0001c0003t0006g0266 a0001c0003t0006g0285 others(2): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136+886C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302013 | |||||||
| chr2:44302104 | ATT | A | 17 | a0001c0002t0003g0233 a0001c0003t0001g0150 a0001c0003t0003g0300 others(14): Show |
17 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1136+978_1136+979d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302104 | |||||||
| chr2:44302115 | A | G | 1 | a0001c0002t0001g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1136+988A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302115 | |||||||
| chr2:44302234 | C | T | 1 | a0001c0002t0002g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1136+1107C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302234 | |||||||
| chr2:44302285 | A | G | 2 | a0001c0003t0001g0294 a0001c0018t0003g0159 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1136+1158A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302285 | |||||||
| chr2:44302289 | C | T | 5 | a0001c0002t0009g0176 a0001c0003t0006g0266 a0001c0003t0006g0285 others(2): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136+1162C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302289 | |||||||
| chr2:44302290 | C | T | 1 | a0001c0002t0002g0246 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1136+1163C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302290 | |||||||
| chr2:44302309 | GATTAA | G | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1136+1187_1136+119 others(9): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44302309 | ||||||
| chr2:44302367 | A | G | 1 | a0001c0002t0002g0183 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1136+1240A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302367 | |||||||
| chr2:44302454 | C | T | 1 | a0001c0003t0002g0119 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1136+1327C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302454 | |||||||
| chr2:44302566 | A | G | 11 | a0001c0002t0002g0164 a0001c0003t0004g0016 a0001c0003t0004g0053 others(8): Show |
11 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1136+1439A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302566 | |||||||
| chr2:44302576 | C | T | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1136+1449C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302576 | |||||||
| chr2:44302583 | C | T | 7 | a0001c0002t0009g0176 a0001c0003t0001g0043 a0001c0003t0006g0266 others(4): Show |
7 | HG01884.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1136+1456C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302583 | |||||||
| chr2:44302650 | T | C | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-1493T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302650 | |||||||
| chr2:44302674 | A | G | 1 | a0001c0002t0003g0233 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1137-1469A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302674 | |||||||
| chr2:44302701 | A | G | 1 | a0001c0002t0003g0233 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1137-1442A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302701 | |||||||
| chr2:44302775 | A | C | 5 | a0001c0003t0004g0016 a0001c0003t0004g0276 a0001c0003t0004g0286 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-1368A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302775 | |||||||
| chr2:44302822 | A | C | 1 | a0001c0002t0002g0231 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1137-1321A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302822 | |||||||
| chr2:44302834 | G | A | 17 | a0001c0002t0003g0233 a0001c0003t0001g0150 a0001c0003t0003g0300 others(14): Show |
17 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1137-1309G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302834 | |||||||
| chr2:44302889 | G | A | 1 | a0001c0003t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1137-1254G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302889 | |||||||
| chr2:44302918 | GCTTGGTG others(14): Show |
G | 1 | a0001c0002t0002g0222 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1137-1224_1137-120 others(25): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302918 | |||||||
| chr2:44302945 | T | A | 20 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(17): Show |
22 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1137-1198T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302945 | |||||||
| chr2:44303062 | G | A | 1 | a0004c0006t0001g0047 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1137-1081G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303062 | |||||||
| chr2:44303093 | C | T | 1 | a0001c0002t0009g0176 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1137-1050C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303093 | |||||||
| chr2:44303128 | G | T | 1 | a0002c0001t0001g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1137-1015G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303128 | |||||||
| chr2:44303181 | ATAAGAG | A | 20 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(17): Show |
22 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1137-958_1137-953d others(8): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303181 | ||||||
| chr2:44303245 | A | AT | 45 | a0001c0002t0002g0197 a0001c0002t0002g0206 a0001c0002t0002g0207 others(42): Show |
47 | HG00280.hp1 HG01069.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.1137-881dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303245 | ||||||
| chr2:44303245 | A | ATT | 153 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(150): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1137-882_1137-881d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303245 | ||||||
| chr2:44303245 | AT | A | 9 | a0001c0002t0002g0179 a0001c0002t0002g0186 a0001c0002t0002g0199 others(6): Show |
9 | HG01167.hp2 HG01975.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.1137-881delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303245 | ||||||
| chr2:44303269 | A | C | 1 | a0001c0003t0003g0303 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1137-874A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303269 | |||||||
| chr2:44303284 | C | T | 189 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1137-859C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303284 | |||||||
| chr2:44303466 | A | T | 29 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(26): Show |
31 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1137-677A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303466 | |||||||
| chr2:44303484 | G | A | 17 | a0001c0002t0003g0233 a0001c0003t0001g0150 a0001c0003t0003g0300 others(14): Show |
17 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1137-659G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303484 | |||||||
| chr2:44303489 | G | T | 1 | a0001c0002t0002g0015 | 2 | NA18980.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1137-654G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303489 | |||||||
| chr2:44303542 | ATG | A | 9 | a0001c0003t0004g0016 a0001c0003t0004g0053 a0001c0003t0004g0276 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1137-597_1137-596d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303542 | ||||||
| chr2:44303559 | T | TG | 20 | a0001c0002t0002g0012 a0001c0002t0002g0179 a0001c0002t0003g0233 others(17): Show |
21 | HG00639.hp1 HG00741.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1137-576dupG | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303559 | ||||||
| chr2:44303559 | TG | T | 209 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(206): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1137-576delG | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303559 | ||||||
| chr2:44303622 | G | A | 2 | a0001c0002t0002g0209 a0001c0002t0002g0224 |
2 | NA18959.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.1137-521G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303622 | |||||||
| chr2:44303688 | G | A | 3 | a0001c0003t0004g0053 a0001c0003t0004g0287 a0001c0003t0004g0291 |
3 | HG02145.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1137-455G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303688 | |||||||
| chr2:44303755 | G | A | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-388G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303755 | |||||||
| chr2:44303790 | C | G | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1137-353C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303790 | |||||||
| chr2:44303801 | A | T | 15 | a0001c0002t0001g0165 a0001c0002t0001g0175 a0001c0003t0001g0009 others(12): Show |
18 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.1137-342A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303801 | |||||||
| chr2:44303809 | C | T | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-334C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303809 | |||||||
| chr2:44303826 | C | T | 19 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(16): Show |
21 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1137-317C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303826 | |||||||
| chr2:44303942 | G | T | 127 | a0001c0003t0002g0109 a0002c0001t0001g0002 a0002c0001t0001g0004 others(124): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1137-201G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303942 | |||||||
| chr2:44304075 | C | A | 1 | a0001c0002t0002g0222 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1137-68C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44304075 | |||||||
| chr2:44304345 | C | T | 168 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(165): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
splice_region_variant&intron_variant | LOW | c.1332+7C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304345 | |||||||
| chr2:44304360 | G | T | 11 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1332+22G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304360 | |||||||
| chr2:44304494 | G | C | 1 | a0002c0001t0010g0316 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1332+156G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304494 | |||||||
| chr2:44304496 | T | C | 34 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(31): Show |
41 | HG00438.hp2 HG00733.hp2 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.1332+158T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304496 | |||||||
| chr2:44304564 | C | T | 4 | a0002c0001t0001g0025 a0002c0001t0001g0026 a0002c0001t0001g0104 others(1): Show |
4 | HG02970.hp2 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332+226C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304564 | |||||||
| chr2:44304768 | C | T | 5 | a0001c0003t0001g0007 a0001c0003t0001g0027 a0001c0003t0001g0028 others(2): Show |
6 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332+430C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304768 | |||||||
| chr2:44304813 | A | AT | 78 | a0001c0002t0002g0012 a0001c0002t0002g0164 a0001c0002t0002g0177 others(75): Show |
81 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.1332+502dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | ||||||
| chr2:44304813 | A | ATT | 75 | a0001c0002t0002g0221 a0001c0003t0001g0150 a0001c0003t0001g0267 others(72): Show |
83 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1332+501_1332+502d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | ||||||
| chr2:44304813 | A | ATTT | 20 | a0001c0003t0001g0294 a0001c0003t0003g0305 a0001c0003t0006g0266 others(17): Show |
20 | HG00323.hp1 HG00642.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1332+500_1332+502d others(5): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | ||||||
| chr2:44304813 | AT | A | 37 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(34): Show |
42 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1332+502delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | ||||||
| chr2:44304813 | ATT | A | 11 | a0001c0002t0001g0175 a0001c0002t0003g0017 a0001c0002t0003g0184 others(8): Show |
12 | HG00280.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1332+501_1332+502d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | ||||||
| chr2:44304813 | ATTTT | A | 11 | a0001c0003t0001g0007 a0001c0003t0001g0027 a0001c0003t0001g0028 others(8): Show |
12 | HG01109.hp2 HG01243.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1332+499_1332+502d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | ||||||
| chr2:44304813 | ATTTTTTT | A | 6 | a0001c0002t0002g0003 a0001c0002t0002g0194 a0001c0002t0002g0228 others(3): Show |
10 | NA18946.hp2 NA18962.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+496_1332+502d others(9): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | ||||||
| chr2:44304813 | ATTTTTTT others(6): Show |
A | 1 | a0002c0001t0001g0051 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1332+490_1332+502d others(15): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | ||||||
| chr2:44304906 | C | T | 1 | a0001c0003t0002g0258 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1332+568C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304906 | |||||||
| chr2:44305000 | T | G | 1 | a0002c0016t0001g0161 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1332+662T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305000 | |||||||
| chr2:44305166 | T | G | 1 | a0001c0003t0003g0315 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1332+828T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305166 | |||||||
| chr2:44305187 | C | T | 25 | a0001c0003t0003g0021 a0001c0003t0004g0016 a0001c0003t0004g0053 others(22): Show |
25 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1332+849C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305187 | |||||||
| chr2:44305328 | T | C | 1 | a0001c0003t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1332+990T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305328 | |||||||
| chr2:44305413 | CCTTT | C | 11 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1332+1080_1332+108 others(8): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44305413 | ||||||
| chr2:44305427 | C | CT | 9 | a0001c0002t0002g0185 a0001c0002t0002g0186 a0001c0002t0002g0187 others(6): Show |
9 | HG01081.hp1 HG01106.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1332+1108dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44305427 | ||||||
| chr2:44305427 | CT | C | 27 | a0001c0002t0001g0165 a0001c0002t0002g0213 a0001c0002t0002g0215 others(24): Show |
30 | HG00280.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1332+1108delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44305427 | ||||||
| chr2:44305427 | CTT | C | 176 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 others(173): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1332+1107_1332+110 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44305427 | ||||||
| chr2:44305427 | CTTT | C | 14 | a0001c0002t0009g0176 a0001c0003t0004g0016 a0001c0003t0004g0053 others(11): Show |
14 | HG01167.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1332+1106_1332+110 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44305427 | ||||||
| chr2:44305429 | T | G | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1332+1091T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305429 | |||||||
| chr2:44305488 | C | T | 6 | a0001c0003t0003g0021 a0001c0018t0003g0159 a0002c0001t0001g0020 others(3): Show |
6 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1332+1150C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305488 | |||||||
| chr2:44305699 | G | A | 15 | a0001c0002t0001g0165 a0001c0002t0001g0175 a0001c0003t0001g0009 others(12): Show |
18 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.1332+1361G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305699 | |||||||
| chr2:44305711 | G | C | 1 | a0001c0003t0001g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1332+1373G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305711 | |||||||
| chr2:44305808 | C | G | 1 | a0002c0016t0001g0161 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1332+1470C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305808 | |||||||
| chr2:44305907 | C | T | 1 | a0001c0003t0002g0037 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1332+1569C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305907 | |||||||
| chr2:44305985 | G | C | 3 | a0001c0003t0004g0053 a0001c0003t0004g0287 a0001c0003t0004g0291 |
3 | HG02145.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1332+1647G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305985 | |||||||
| chr2:44306071 | T | G | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1332+1733T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306071 | |||||||
| chr2:44306140 | G | T | 10 | a0001c0002t0001g0175 a0001c0003t0004g0016 a0001c0003t0004g0276 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+1802G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306140 | |||||||
| chr2:44306205 | T | C | 1 | a0001c0003t0004g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1332+1867T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306205 | |||||||
| chr2:44306258 | G | A | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+1920G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306258 | |||||||
| chr2:44306524 | C | T | 10 | a0001c0003t0002g0258 a0001c0003t0004g0016 a0001c0003t0004g0053 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+2186C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306524 | |||||||
| chr2:44306550 | C | CT | 46 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 others(43): Show |
52 | HG00323.hp2 HG00438.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1332+2234dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44306550 | ||||||
| chr2:44306550 | C | T | 1 | a0001c0002t0002g0228 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1332+2212C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306550 | |||||||
| chr2:44306550 | CT | C | 144 | a0001c0002t0001g0181 a0001c0002t0002g0227 a0001c0002t0009g0176 others(141): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1332+2234delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44306550 | ||||||
| chr2:44306550 | CTT | C | 8 | a0001c0002t0001g0175 a0001c0003t0001g0294 a0001c0003t0003g0021 others(5): Show |
8 | HG02257.hp2 HG02970.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1332+2233_1332+223 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44306550 | ||||||
| chr2:44306550 | CTTT | C | 23 | a0001c0003t0004g0016 a0001c0003t0004g0053 a0001c0003t0004g0276 others(20): Show |
23 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1332+2232_1332+223 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44306550 | ||||||
| chr2:44306586 | G | C | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1332+2248G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306586 | |||||||
| chr2:44306594 | C | T | 10 | a0001c0003t0004g0016 a0001c0003t0004g0053 a0001c0003t0004g0276 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+2256C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306594 | |||||||
| chr2:44306807 | T | C | 14 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(11): Show |
16 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1332+2469T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306807 | |||||||
| chr2:44306858 | A | C | 1 | a0001c0002t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1332+2520A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306858 | |||||||
| chr2:44306873 | A | C | 132 | a0001c0003t0002g0109 a0002c0001t0001g0002 a0002c0001t0001g0004 others(129): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1332+2535A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306873 | |||||||
| chr2:44307021 | G | C | 2 | a0002c0001t0001g0090 a0002c0001t0001g0091 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1332+2683G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307021 | |||||||
| chr2:44307048 | C | T | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1332+2710C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307048 | |||||||
| chr2:44307128 | C | T | 1 | a0001c0003t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1332+2790C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307128 | |||||||
| chr2:44307182 | C | A | 91 | a0001c0003t0002g0109 a0002c0001t0001g0002 a0002c0001t0001g0004 others(88): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1332+2844C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307182 | |||||||
| chr2:44307220 | C | A | 26 | a0001c0003t0003g0021 a0001c0003t0004g0016 a0001c0003t0004g0053 others(23): Show |
26 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1332+2882C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307220 | |||||||
| chr2:44307275 | T | C | 8 | a0001c0002t0001g0181 a0001c0003t0001g0006 a0001c0003t0001g0248 others(5): Show |
10 | HG01106.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+2937T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307275 | |||||||
| chr2:44307278 | C | T | 233 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(230): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1332+2940C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307278 | |||||||
| chr2:44307333 | A | C | 183 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(180): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1332+2995A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307333 | |||||||
| chr2:44307363 | T | C | 4 | a0002c0001t0001g0025 a0002c0001t0001g0026 a0002c0001t0001g0104 others(1): Show |
4 | HG02970.hp2 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332+3025T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307363 | |||||||
| chr2:44307425 | C | A | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1332+3087C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307425 | |||||||
| chr2:44307564 | AT | A | 167 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(164): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1332+3243delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44307564 | ||||||
| chr2:44307564 | ATT | A | 18 | a0001c0003t0001g0040 a0001c0003t0001g0294 a0001c0003t0003g0021 others(15): Show |
18 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1332+3242_1332+324 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44307564 | ||||||
| chr2:44307895 | T | C | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+3557T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307895 | |||||||
| chr2:44308139 | A | G | 1 | a0001c0003t0003g0284 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1332+3801A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308139 | |||||||
| chr2:44308149 | C | G | 2 | a0001c0003t0001g0039 a0001c0003t0001g0041 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1332+3811C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308149 | |||||||
| chr2:44308208 | A | G | 4 | a0001c0003t0001g0062 a0001c0003t0001g0250 a0001c0003t0001g0251 others(1): Show |
4 | HG03130.hp1 HG03486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332+3870A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308208 | |||||||
| chr2:44308274 | G | A | 1 | a0002c0001t0001g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1332+3936G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308274 | |||||||
| chr2:44308315 | T | A | 1 | a0001c0003t0001g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1332+3977T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308315 | |||||||
| chr2:44308380 | G | C | 87 | a0001c0003t0002g0109 a0002c0001t0001g0002 a0002c0001t0001g0004 others(84): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1332+4042G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308380 | |||||||
| chr2:44308547 | G | A | 215 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(212): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1333-4039G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308547 | |||||||
| chr2:44308555 | C | T | 8 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(5): Show |
9 | HG00280.hp1 HG00738.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1333-4031C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308555 | |||||||
| chr2:44308573 | T | C | 1 | a0001c0003t0001g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1333-4013T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308573 | |||||||
| chr2:44308599 | G | T | 25 | a0001c0003t0003g0021 a0001c0003t0004g0016 a0001c0003t0004g0053 others(22): Show |
25 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1333-3987G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308599 | |||||||
| chr2:44308732 | A | AT | 7 | a0001c0002t0002g0222 a0001c0002t0003g0017 a0001c0002t0003g0184 others(4): Show |
8 | HG00280.hp1 HG01070.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.1333-3841dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44308732 | ||||||
| chr2:44308798 | TCTCAG | T | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1333-3783_1333-377 others(9): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44308798 | ||||||
| chr2:44308819 | G | A | 24 | a0001c0003t0003g0021 a0001c0003t0004g0016 a0001c0003t0004g0053 others(21): Show |
24 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1333-3767G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308819 | |||||||
| chr2:44308836 | C | T | 3 | a0002c0001t0001g0020 a0002c0001t0001g0022 a0002c0001t0001g0024 |
3 | HG04115.hp2 HG04199.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1333-3750C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308836 | |||||||
| chr2:44308845 | G | C | 1 | a0001c0002t0001g0174 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1333-3741G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308845 | |||||||
| chr2:44308922 | C | T | 1 | a0001c0003t0002g0084 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1333-3664C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308922 | |||||||
| chr2:44308933 | C | T | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1333-3653C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308933 | |||||||
| chr2:44309110 | A | G | 141 | a0001c0003t0001g0008 a0001c0003t0001g0031 a0001c0003t0001g0062 others(138): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1333-3476A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309110 | |||||||
| chr2:44309223 | C | A | 15 | a0001c0002t0003g0233 a0001c0003t0002g0101 a0001c0003t0003g0301 others(12): Show |
15 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1333-3363C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309223 | |||||||
| chr2:44309233 | C | G | 5 | a0001c0002t0009g0176 a0001c0003t0004g0289 a0001c0003t0006g0266 others(2): Show |
5 | HG01109.hp2 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333-3353C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309233 | |||||||
| chr2:44309407 | T | C | 178 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(175): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1333-3179T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309407 | |||||||
| chr2:44309494 | TG | T | 15 | a0001c0002t0002g0222 a0001c0002t0003g0017 a0001c0002t0003g0184 others(12): Show |
17 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1333-3090delG | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44309494 | ||||||
| chr2:44309538 | C | T | 5 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 others(2): Show |
5 | HG00738.hp2 HG00741.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333-3048C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309538 | |||||||
| chr2:44309567 | C | T | 6 | a0001c0002t0009g0176 a0001c0003t0004g0289 a0001c0003t0006g0266 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333-3019C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309567 | |||||||
| chr2:44309577 | G | T | 1 | a0001c0002t0002g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1333-3009G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309577 | |||||||
| chr2:44309682 | C | G | 6 | a0001c0002t0009g0176 a0001c0003t0004g0289 a0001c0003t0006g0266 others(3): Show |
6 | HG01109.hp2 HG01884.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333-2904C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309682 | |||||||
| chr2:44309721 | C | G | 1 | a0002c0001t0001g0075 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1333-2865C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309721 | |||||||
| chr2:44309789 | G | T | 17 | a0001c0002t0003g0233 a0001c0003t0001g0150 a0001c0003t0003g0300 others(14): Show |
17 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1333-2797G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309789 | |||||||
| chr2:44309889 | T | G | 2 | a0002c0001t0001g0268 a0002c0001t0001g0270 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1333-2697T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309889 | |||||||
| chr2:44309897 | C | CT | 22 | a0001c0002t0001g0168 a0001c0002t0001g0169 a0001c0002t0001g0175 others(19): Show |
23 | HG00741.hp1 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1333-2680dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44309897 | ||||||
| chr2:44310162 | G | A | 2 | a0004c0006t0001g0045 a0004c0006t0001g0047 |
2 | NA18969.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1333-2424G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310162 | |||||||
| chr2:44310224 | G | T | 1 | a0011c0012t0001g0078 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1333-2362G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310224 | |||||||
| chr2:44310258 | G | A | 1 | a0002c0001t0001g0066 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1333-2328G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310258 | |||||||
| chr2:44310283 | C | T | 2 | a0001c0003t0003g0304 a0001c0003t0003g0308 |
2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1333-2303C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310283 | |||||||
| chr2:44310337 | A | G | 1 | a0002c0001t0001g0051 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1333-2249A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310337 | |||||||
| chr2:44310428 | GTTCT | G | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1333-2150_1333-214 others(8): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44310428 | ||||||
| chr2:44310603 | G | A | 1 | a0001c0002t0002g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1333-1983G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310603 | |||||||
| chr2:44310631 | G | C | 1 | a0001c0002t0002g0221 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1333-1955G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310631 | |||||||
| chr2:44310652 | C | T | 1 | a0001c0002t0002g0202 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1333-1934C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310652 | |||||||
| chr2:44310682 | G | A | 1 | a0002c0001t0010g0316 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1333-1904G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310682 | |||||||
| chr2:44310689 | G | T | 1 | a0001c0003t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1333-1897G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310689 | |||||||
| chr2:44310690 | C | A | 1 | a0001c0003t0001g0062 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1333-1896C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310690 | |||||||
| chr2:44310692 | A | AT | 10 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(7): Show |
10 | HG01256.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1333-1884dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44310692 | ||||||
| chr2:44310805 | G | GT | 17 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(14): Show |
19 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1333-1770dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44310805 | ||||||
| chr2:44310839 | C | T | 1 | a0002c0001t0001g0066 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1333-1747C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310839 | |||||||
| chr2:44310941 | C | T | 20 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(17): Show |
22 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1333-1645C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310941 | |||||||
| chr2:44311097 | ATTC | A | 6 | a0001c0002t0009g0176 a0001c0003t0004g0289 a0001c0003t0006g0266 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333-1483_1333-148 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44311097 | ||||||
| chr2:44311107 | T | G | 1 | a0001c0017t0007g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1333-1479T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311107 | |||||||
| chr2:44311302 | C | A | 1 | a0002c0001t0001g0071 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1333-1284C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311302 | |||||||
| chr2:44311345 | A | G | 217 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(214): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1333-1241A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311345 | |||||||
| chr2:44311394 | A | G | 1 | a0001c0002t0002g0264 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1333-1192A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311394 | |||||||
| chr2:44311594 | G | A | 3 | a0001c0003t0004g0053 a0001c0003t0004g0287 a0001c0003t0004g0291 |
3 | HG02145.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1333-992G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311594 | |||||||
| chr2:44311602 | A | G | 1 | a0008c0014t0001g0319 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1333-984A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311602 | |||||||
| chr2:44311723 | T | TA | 171 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(168): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1333-850dupA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44311723 | ||||||
| chr2:44311723 | T | TAA | 16 | a0001c0003t0004g0053 a0001c0003t0004g0278 a0001c0003t0004g0279 others(13): Show |
16 | HG00735.hp2 HG01433.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1333-851_1333-850d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44311723 | ||||||
| chr2:44311723 | T | TTA | 3 | a0002c0004t0001g0170 a0002c0004t0001g0171 a0002c0004t0001g0173 |
3 | HG02647.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1333-863_1333-862i others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311723 | |||||||
| chr2:44311737 | C | A | 18 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(15): Show |
20 | HG00280.hp1 HG00738.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1333-849C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311737 | |||||||
| chr2:44311790 | G | T | 1 | a0001c0003t0004g0291 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1333-796G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311790 | |||||||
| chr2:44311793 | C | T | 7 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1333-793C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311793 | |||||||
| chr2:44311797 | C | T | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333-789C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311797 | |||||||
| chr2:44311824 | G | A | 17 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(14): Show |
19 | HG00280.hp1 HG00738.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1333-762G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311824 | |||||||
| chr2:44311870 | C | T | 213 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(210): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1333-716C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311870 | |||||||
| chr2:44311900 | G | A | 1 | a0002c0001t0001g0117 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1333-686G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311900 | |||||||
| chr2:44311902 | A | G | 176 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(173): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1333-684A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311902 | |||||||
| chr2:44312007 | G | GATTTAAA others(23): Show |
1 | a0002c0001t0001g0072 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1333-568_1333-539d others(32): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44312007 | ||||||
| chr2:44312039 | T | G | 1 | a0001c0003t0004g0288 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1333-547T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312039 | |||||||
| chr2:44312148 | T | G | 11 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1333-438T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312148 | |||||||
| chr2:44312167 | T | C | 26 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(23): Show |
33 | HG00438.hp2 HG00733.hp2 HG02040.hp1 others(30): Show |
intron_variant | MODIFIER | c.1333-419T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312167 | |||||||
| chr2:44312279 | T | G | 1 | a0001c0002t0003g0184 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1333-307T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312279 | |||||||
| chr2:44312280 | G | C | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1333-306G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312280 | |||||||
| chr2:44312361 | T | C | 1 | a0001c0002t0002g0183 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1333-225T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312361 | |||||||
| chr2:44312375 | C | T | 1 | a0001c0003t0001g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1333-211C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312375 | |||||||
| chr2:44312504 | G | A | 1 | a0001c0003t0002g0258 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1333-82G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312504 | |||||||
| chr2:44312564 | C | G | 2 | a0002c0001t0001g0132 a0002c0001t0001g0153 |
2 | NA18985.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1333-22C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312564 | |||||||
| chr2:44312574 | T | A | 1 | a0001c0002t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1333-12T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312574 | |||||||
| chr2:44312774 | C | CAGCTATA others(8): Show |
10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1500+21_1500+22ins others(15): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44312774 | |||||||
| chr2:44312779 | C | T | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1500+26C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44312779 | |||||||
| chr2:44312781 | T | TACTA | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1500+28_1500+29ins others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44312781 | |||||||
| chr2:44312782 | C | T | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1500+29C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44312782 | |||||||
| chr2:44312831 | A | C | 1 | a0001c0003t0001g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1500+78A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44312831 | |||||||
| chr2:44313041 | G | C | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1500+288G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313041 | |||||||
| chr2:44313080 | G | A | 11 | a0001c0003t0001g0007 a0001c0003t0001g0027 a0001c0003t0001g0028 others(8): Show |
12 | HG00738.hp1 HG01109.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1500+327G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313080 | |||||||
| chr2:44313102 | C | T | 210 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(207): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1500+349C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313102 | |||||||
| chr2:44313261 | C | T | 1 | a0002c0004t0001g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1500+508C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313261 | |||||||
| chr2:44313266 | G | C | 8 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(5): Show |
9 | HG00280.hp1 HG01070.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1500+513G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313266 | |||||||
| chr2:44313293 | C | T | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1500+540C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313293 | |||||||
| chr2:44313316 | C | A | 1 | a0001c0003t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1501-519C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313316 | |||||||
| chr2:44313320 | G | C | 1 | a0001c0002t0009g0176 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1501-515G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313320 | |||||||
| chr2:44313409 | G | A | 9 | a0001c0003t0004g0016 a0001c0003t0004g0053 a0001c0003t0004g0276 others(6): Show |
9 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1501-426G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313409 | |||||||
| chr2:44313442 | C | T | 5 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 others(2): Show |
5 | HG00738.hp2 HG00741.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1501-393C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313442 | |||||||
| chr2:44313470 | T | C | 1 | a0001c0002t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1501-365T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313470 | |||||||
| chr2:44313598 | T | C | 1 | a0002c0001t0001g0092 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1501-237T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313598 | |||||||
| chr2:44313735 | G | C | 1 | a0001c0003t0003g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1501-100G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313735 | |||||||
| chr2:44314009 | G | C | 1 | a0002c0001t0001g0133 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1617+58G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314009 | |||||||
| chr2:44314118 | T | C | 1 | a0001c0003t0001g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1617+167T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314118 | |||||||
| chr2:44314203 | C | G | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617+252C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314203 | |||||||
| chr2:44314291 | G | GAGA | 5 | a0001c0003t0001g0007 a0001c0003t0001g0027 a0001c0003t0001g0028 others(2): Show |
6 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617+341_1617+343d others(5): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314291 | ||||||
| chr2:44314332 | G | GATCA | 4 | a0002c0001t0001g0134 a0002c0001t0001g0151 a0002c0001t0001g0152 others(1): Show |
4 | HG02056.hp1 HG02071.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1617+391_1617+394d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314332 | ||||||
| chr2:44314373 | C | T | 11 | a0001c0002t0009g0176 a0001c0003t0001g0007 a0001c0003t0001g0027 others(8): Show |
12 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1617+422C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314373 | |||||||
| chr2:44314549 | A | G | 3 | a0001c0003t0004g0053 a0001c0003t0004g0287 a0001c0003t0004g0291 |
3 | HG02145.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1617+598A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314549 | |||||||
| chr2:44314560 | G | A | 1 | a0001c0002t0002g0232 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1617+609G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314560 | |||||||
| chr2:44314567 | G | C | 216 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(213): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1617+616G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314567 | |||||||
| chr2:44314586 | C | T | 169 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(166): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1617+635C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314586 | |||||||
| chr2:44314592 | C | CCA | 174 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(171): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1617+657_1617+658d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314592 | ||||||
| chr2:44314592 | C | CCACA | 3 | a0001c0003t0001g0248 a0001c0017t0007g0162 a0002c0001t0001g0132 |
3 | HG02055.hp1 HG02922.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1617+655_1617+658d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314592 | ||||||
| chr2:44314592 | CCA | C | 30 | a0001c0002t0009g0176 a0001c0003t0001g0007 a0001c0003t0001g0027 others(27): Show |
31 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1617+657_1617+658d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314592 | ||||||
| chr2:44314612 | T | A | 5 | a0001c0003t0001g0007 a0001c0003t0001g0027 a0001c0003t0001g0028 others(2): Show |
6 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617+661T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314612 | |||||||
| chr2:44314665 | A | G | 1 | a0001c0003t0013g0293 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1617+714A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314665 | |||||||
| chr2:44314718 | C | G | 16 | a0001c0002t0003g0233 a0001c0003t0001g0150 a0001c0003t0003g0300 others(13): Show |
16 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.1617+767C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314718 | |||||||
| chr2:44314757 | T | C | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1617+806T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314757 | |||||||
| chr2:44314778 | AAT | A | 171 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(168): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1617+834_1617+835d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314778 | ||||||
| chr2:44314858 | T | G | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1617+907T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314858 | |||||||
| chr2:44314900 | G | A | 5 | a0001c0003t0004g0016 a0001c0003t0004g0276 a0001c0003t0004g0286 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1617+949G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314900 | |||||||
| chr2:44314905 | T | C | 1 | a0001c0003t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1617+954T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314905 | |||||||
| chr2:44314922 | A | AT | 176 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(173): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1617+997dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314922 | ||||||
| chr2:44314922 | A | ATT | 46 | a0001c0002t0002g0211 a0001c0002t0002g0232 a0001c0002t0002g0242 others(43): Show |
49 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1617+996_1617+997d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314922 | ||||||
| chr2:44314922 | AT | A | 6 | a0001c0002t0001g0181 a0001c0002t0002g0210 a0001c0002t0009g0176 others(3): Show |
6 | HG01257.hp1 HG02818.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617+997delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314922 | ||||||
| chr2:44314922 | ATTTTTTT others(5): Show |
A | 17 | a0001c0002t0001g0165 a0001c0002t0001g0175 a0001c0003t0001g0009 others(14): Show |
20 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617+986_1617+997d others(14): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314922 | ||||||
| chr2:44315008 | C | T | 13 | a0001c0002t0001g0165 a0001c0003t0001g0009 a0001c0003t0001g0010 others(10): Show |
16 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1617+1057C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315008 | |||||||
| chr2:44315022 | C | G | 7 | a0001c0002t0001g0181 a0001c0003t0001g0006 a0001c0003t0001g0248 others(4): Show |
9 | HG01106.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1617+1071C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315022 | |||||||
| chr2:44315051 | C | T | 5 | a0001c0003t0001g0007 a0001c0003t0001g0027 a0001c0003t0001g0028 others(2): Show |
6 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617+1100C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315051 | |||||||
| chr2:44315080 | C | T | 9 | a0001c0002t0001g0181 a0001c0003t0001g0006 a0001c0003t0001g0248 others(6): Show |
11 | HG01106.hp2 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1617+1129C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315080 | |||||||
| chr2:44315145 | G | A | 5 | a0001c0002t0009g0176 a0001c0003t0006g0266 a0001c0003t0006g0285 others(2): Show |
5 | HG02886.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1617+1194G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315145 | |||||||
| chr2:44315184 | C | T | 1 | a0001c0002t0002g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1617+1233C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315184 | |||||||
| chr2:44315194 | C | T | 1 | a0001c0003t0001g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1617+1243C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315194 | |||||||
| chr2:44315379 | T | C | 1 | a0002c0001t0001g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1617+1428T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315379 | |||||||
| chr2:44315455 | C | T | 1 | a0001c0003t0003g0314 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1617+1504C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315455 | |||||||
| chr2:44315500 | C | T | 1 | a0001c0002t0002g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1617+1549C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315500 | |||||||
| chr2:44315501 | G | A | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617+1550G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315501 | |||||||
| chr2:44315503 | C | CA | 33 | a0001c0002t0002g0160 a0001c0002t0002g0185 a0001c0002t0002g0186 others(30): Show |
33 | HG01081.hp1 HG01106.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.1617+1567dupA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44315503 | ||||||
| chr2:44315503 | CA | C | 209 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(206): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1617+1567delA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44315503 | ||||||
| chr2:44315509 | A | G | 1 | a0001c0002t0002g0198 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1617+1558A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315509 | |||||||
| chr2:44315598 | G | C | 1 | a0002c0001t0001g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1617+1647G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315598 | |||||||
| chr2:44315653 | C | CA | 77 | a0001c0002t0001g0167 a0001c0002t0001g0169 a0001c0002t0001g0175 others(74): Show |
81 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.1617+1724dupA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44315653 | ||||||
| chr2:44315653 | C | CAA | 106 | a0001c0002t0001g0168 a0001c0002t0003g0017 a0001c0002t0003g0184 others(103): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1617+1723_1617+172 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44315653 | ||||||
| chr2:44315653 | C | CAAA | 13 | a0001c0002t0003g0260 a0001c0003t0003g0321 a0001c0003t0004g0287 others(10): Show |
13 | HG00423.hp1 HG01109.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.1617+1722_1617+172 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44315653 | ||||||
| chr2:44315698 | TAAAACAT others(20): Show |
T | 1 | a0001c0002t0009g0176 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1617+1749_1617+177 others(31): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44315698 | ||||||
| chr2:44315724 | T | G | 1 | a0002c0001t0001g0093 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1617+1773T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315724 | |||||||
| chr2:44315884 | G | C | 9 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(6): Show |
10 | HG00280.hp1 HG00738.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617+1933G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315884 | |||||||
| chr2:44315958 | C | A | 3 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0253 |
3 | HG03130.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1617+2007C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315958 | |||||||
| chr2:44315986 | C | G | 215 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(212): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1617+2035C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315986 | |||||||
| chr2:44316104 | G | A | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1617+2153G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316104 | |||||||
| chr2:44316164 | C | G | 10 | a0001c0003t0004g0016 a0001c0003t0004g0053 a0001c0003t0004g0276 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617+2213C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316164 | |||||||
| chr2:44316178 | C | T | 214 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(211): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1617+2227C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316178 | |||||||
| chr2:44316250 | T | A | 135 | a0001c0003t0001g0008 a0001c0003t0001g0031 a0001c0003t0003g0320 others(132): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1617+2299T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316250 | |||||||
| chr2:44316252 | T | C | 1 | a0001c0003t0001g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1617+2301T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316252 | |||||||
| chr2:44316273 | A | T | 1 | a0001c0003t0004g0278 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1617+2322A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316273 | |||||||
| chr2:44316295 | G | C | 1 | a0001c0002t0001g0174 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1617+2344G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316295 | |||||||
| chr2:44316345 | C | T | 1 | a0001c0003t0006g0285 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1617+2394C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316345 | |||||||
| chr2:44316455 | CAAAG | C | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617+2507_1617+251 others(8): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44316455 | ||||||
| chr2:44316851 | C | T | 1 | a0001c0003t0003g0303 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1617+2900C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316851 | |||||||
| chr2:44316880 | A | G | 1 | a0001c0003t0002g0258 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1617+2929A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316880 | |||||||
| chr2:44316885 | A | G | 1 | a0001c0003t0013g0293 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1617+2934A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316885 | |||||||
| chr2:44316900 | G | T | 1 | a0002c0001t0001g0055 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1617+2949G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316900 | |||||||
| chr2:44316902 | T | C | 1 | a0002c0001t0001g0055 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1617+2951T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316902 | |||||||
| chr2:44316976 | T | A | 24 | a0001c0002t0002g0160 a0001c0002t0002g0185 a0001c0002t0002g0186 others(21): Show |
24 | HG01081.hp1 HG01106.hp1 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.1617+3025T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316976 | |||||||
| chr2:44316983 | C | G | 1 | a0002c0001t0001g0074 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1617+3032C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316983 | |||||||
| chr2:44317035 | G | A | 10 | a0001c0003t0004g0278 a0001c0003t0004g0279 a0001c0003t0004g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617+3084G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317035 | |||||||
| chr2:44317073 | G | C | 1 | a0002c0001t0001g0134 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1617+3122G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317073 | |||||||
| chr2:44317091 | A | G | 3 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0253 |
3 | HG03130.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1618-3108A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317091 | |||||||
| chr2:44317125 | C | G | 11 | a0001c0003t0001g0257 a0001c0003t0004g0278 a0001c0003t0004g0279 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1618-3074C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317125 | |||||||
| chr2:44317187 | G | T | 1 | a0002c0001t0001g0145 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1618-3012G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317187 | |||||||
| chr2:44317201 | G | A | 5 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(2): Show |
5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1618-2998G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317201 | |||||||
| chr2:44317339 | G | T | 7 | a0001c0002t0001g0181 a0001c0003t0001g0006 a0001c0003t0001g0248 others(4): Show |
9 | HG01106.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1618-2860G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317339 | |||||||
| chr2:44317459 | C | CA | 57 | a0001c0002t0002g0220 a0001c0002t0002g0224 a0001c0002t0002g0235 others(54): Show |
58 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1618-2724dupA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44317459 | ||||||
| chr2:44317459 | C | CAA | 169 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(166): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1618-2725_1618-272 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44317459 | ||||||
| chr2:44317459 | C | CAAA | 7 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0253 others(4): Show |
7 | HG00735.hp2 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618-2726_1618-272 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44317459 | ||||||
| chr2:44317567 | T | G | 1 | a0001c0003t0004g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1618-2632T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317567 | |||||||
| chr2:44317646 | T | A | 3 | a0002c0004t0001g0170 a0002c0004t0001g0171 a0002c0004t0001g0173 |
3 | HG02647.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1618-2553T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317646 | |||||||
| chr2:44317667 | TATTTTCA others(34): Show |
T | 1 | a0001c0003t0004g0287 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1618-2519_1618-247 others(45): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44317667 | ||||||
| chr2:44317775 | A | C | 29 | a0002c0001t0001g0056 a0002c0001t0001g0057 a0002c0001t0001g0058 others(26): Show |
29 | HG00597.hp2 HG01358.hp1 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.1618-2424A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317775 | |||||||
| chr2:44317797 | C | T | 1 | a0001c0002t0002g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1618-2402C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317797 | |||||||
| chr2:44317810 | G | A | 5 | a0001c0002t0009g0176 a0001c0003t0006g0266 a0001c0003t0006g0285 others(2): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618-2389G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317810 | |||||||
| chr2:44317816 | G | A | 173 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(170): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1618-2383G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317816 | |||||||
| chr2:44317953 | G | C | 1 | a0001c0002t0002g0263 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1618-2246G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317953 | |||||||
| chr2:44317959 | AAAT | A | 7 | a0001c0002t0001g0181 a0001c0003t0001g0006 a0001c0003t0001g0248 others(4): Show |
9 | HG01106.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1618-2235_1618-223 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44317959 | ||||||
| chr2:44317973 | T | G | 5 | a0002c0001t0001g0025 a0002c0001t0001g0026 a0002c0001t0001g0065 others(2): Show |
5 | HG02055.hp2 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618-2226T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317973 | |||||||
| chr2:44317987 | T | C | 2 | a0001c0002t0002g0003 a0001c0002t0002g0261 |
6 | NA18962.hp1 NA18979.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618-2212T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317987 | |||||||
| chr2:44318093 | CTG | C | 19 | a0001c0003t0004g0016 a0001c0003t0004g0276 a0001c0003t0004g0278 others(16): Show |
19 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1618-2104_1618-210 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318093 | ||||||
| chr2:44318095 | G | GT | 7 | a0001c0002t0002g0215 a0001c0002t0002g0241 a0001c0002t0002g0247 others(4): Show |
7 | HG01978.hp1 HG02004.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1618-2089dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318095 | ||||||
| chr2:44318095 | GT | G | 152 | a0001c0002t0001g0180 a0001c0002t0001g0181 a0001c0003t0001g0006 others(149): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1618-2089delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318095 | ||||||
| chr2:44318095 | GTT | G | 25 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(22): Show |
28 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1618-2090_1618-208 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318095 | ||||||
| chr2:44318095 | GTTT | G | 11 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0260 others(8): Show |
12 | HG00280.hp1 HG00738.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.1618-2091_1618-208 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318095 | ||||||
| chr2:44318159 | C | T | 9 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0260 others(6): Show |
10 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1618-2040C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318159 | |||||||
| chr2:44318252 | G | A | 5 | a0001c0002t0009g0176 a0001c0003t0006g0266 a0001c0003t0006g0285 others(2): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618-1947G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318252 | |||||||
| chr2:44318282 | G | A | 1 | a0002c0004t0001g0172 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1618-1917G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318282 | |||||||
| chr2:44318312 | G | C | 4 | a0001c0002t0002g0012 a0001c0002t0002g0178 a0001c0002t0002g0179 others(1): Show |
5 | HG01074.hp1 HG01099.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618-1887G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318312 | |||||||
| chr2:44318345 | C | A | 1 | a0001c0002t0001g0174 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1618-1854C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318345 | |||||||
| chr2:44318356 | G | C | 3 | a0002c0001t0001g0106 a0002c0001t0001g0107 a0002c0001t0001g0108 |
3 | NA18999.hp2 NA19057.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1618-1843G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318356 | |||||||
| chr2:44318403 | T | G | 1 | a0009c0015t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1618-1796T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318403 | |||||||
| chr2:44318406 | T | G | 10 | a0001c0003t0004g0016 a0001c0003t0004g0053 a0001c0003t0004g0276 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1618-1793T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318406 | |||||||
| chr2:44318437 | T | C | 188 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(185): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1618-1762T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318437 | |||||||
| chr2:44318566 | C | G | 1 | a0001c0002t0002g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1618-1633C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318566 | |||||||
| chr2:44318573 | T | G | 2 | a0002c0001t0001g0020 a0002c0001t0001g0022 |
2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1618-1626T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318573 | |||||||
| chr2:44318596 | A | ATG | 4 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(1): Show |
4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1602_1618-160 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318596 | ||||||
| chr2:44318598 | A | T | 4 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(1): Show |
4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1601A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318598 | |||||||
| chr2:44318601 | A | C | 4 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(1): Show |
4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1598A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318601 | |||||||
| chr2:44318601 | A | T | 202 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1618-1598A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318601 | |||||||
| chr2:44318602 | A | T | 202 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1618-1597A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318602 | |||||||
| chr2:44318603 | A | T | 206 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(203): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1618-1596A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318603 | |||||||
| chr2:44318604 | T | A | 4 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(1): Show |
4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1595T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318604 | |||||||
| chr2:44318604 | T | G | 202 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1618-1595T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318604 | |||||||
| chr2:44318605 | G | C | 202 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1618-1594G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318605 | |||||||
| chr2:44318606 | A | G | 4 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(1): Show |
4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1593A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318606 | |||||||
| chr2:44318607 | T | C | 4 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(1): Show |
4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1592T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318607 | |||||||
| chr2:44318609 | C | G | 202 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1618-1590C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318609 | |||||||
| chr2:44318610 | A | G | 202 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1618-1589A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318610 | |||||||
| chr2:44318611 | T | C | 202 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1618-1588T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318611 | |||||||
| chr2:44318611 | T | G | 4 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(1): Show |
4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1588T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318611 | |||||||
| chr2:44318612 | T | A | 206 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(203): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1618-1587T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318612 | |||||||
| chr2:44318613 | C | A | 4 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(1): Show |
4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1586C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318613 | |||||||
| chr2:44318614 | T | A | 202 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1618-1585T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318614 | |||||||
| chr2:44318615 | GTGCC | G | 4 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(1): Show |
4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1582_1618-157 others(8): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318615 | ||||||
| chr2:44318616 | T | A | 202 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1618-1583T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318616 | |||||||
| chr2:44318617 | G | A | 202 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1618-1582G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318617 | |||||||
| chr2:44318618 | C | T | 202 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1618-1581C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318618 | |||||||
| chr2:44318619 | C | G | 202 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(199): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1618-1580C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318619 | |||||||
| chr2:44318623 | G | C | 206 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(203): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1618-1576G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318623 | |||||||
| chr2:44318624 | C | A | 206 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(203): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1618-1575C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318624 | |||||||
| chr2:44318625 | A | T | 206 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(203): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1618-1574A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318625 | |||||||
| chr2:44318626 | A | T | 206 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(203): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1618-1573A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318626 | |||||||
| chr2:44318627 | A | T | 206 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(203): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1618-1572A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318627 | |||||||
| chr2:44318637 | C | A | 4 | a0001c0003t0003g0021 a0002c0001t0001g0020 a0002c0001t0001g0022 others(1): Show |
4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1562C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318637 | |||||||
| chr2:44318713 | T | C | 1 | a0002c0001t0001g0055 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1618-1486T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318713 | |||||||
| chr2:44318737 | T | C | 1 | a0001c0003t0012g0292 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1618-1462T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318737 | |||||||
| chr2:44318877 | C | T | 210 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(207): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1618-1322C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318877 | |||||||
| chr2:44318945 | A | C | 1 | a0001c0002t0002g0220 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1618-1254A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318945 | |||||||
| chr2:44319036 | CAT | C | 3 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0001g0253 |
3 | HG03130.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1618-1162_1618-116 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319036 | |||||||
| chr2:44319040 | T | C | 1 | a0001c0003t0002g0037 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1618-1159T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319040 | |||||||
| chr2:44319264 | T | A | 3 | a0001c0003t0001g0009 a0001c0003t0001g0035 a0001c0003t0001g0142 |
4 | HG02647.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1618-935T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319264 | |||||||
| chr2:44319287 | A | T | 1 | a0002c0001t0001g0145 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1618-912A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319287 | |||||||
| chr2:44319367 | T | C | 1 | a0001c0003t0003g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1618-832T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319367 | |||||||
| chr2:44319454 | G | C | 1 | a0001c0018t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1618-745G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319454 | |||||||
| chr2:44319462 | C | A | 5 | a0001c0002t0009g0176 a0001c0003t0006g0266 a0001c0003t0006g0285 others(2): Show |
5 | HG01884.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618-737C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319462 | |||||||
| chr2:44319493 | CATTT | C | 26 | a0002c0001t0001g0057 a0002c0001t0001g0058 a0002c0001t0001g0060 others(23): Show |
26 | HG00597.hp2 HG01358.hp1 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.1618-703_1618-700d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44319493 | ||||||
| chr2:44319562 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1618-637T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319562 | |||||||
| chr2:44319602 | T | C | 137 | a0001c0017t0007g0162 a0002c0001t0001g0002 a0002c0001t0001g0004 others(134): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1618-597T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319602 | |||||||
| chr2:44319634 | T | A | 1 | a0001c0003t0003g0284 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1618-565T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319634 | |||||||
| chr2:44319694 | T | C | 4 | a0001c0002t0002g0013 a0001c0002t0002g0190 a0001c0002t0002g0238 others(1): Show |
5 | HG02040.hp2 HG02155.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618-505T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319694 | |||||||
| chr2:44319992 | A | G | 189 | a0001c0002t0001g0165 a0001c0002t0001g0167 a0001c0002t0001g0168 others(186): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1618-207A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319992 | |||||||
| chr2:44320003 | A | G | 10 | a0001c0002t0003g0017 a0001c0002t0003g0184 a0001c0002t0003g0259 others(7): Show |
11 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1618-196A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44320003 | |||||||
| chr2:44320057 | A | T | 1 | a0002c0001t0001g0130 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1618-142A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44320057 | |||||||
| chr2:44320097 | G | C | 20 | a0001c0003t0004g0016 a0001c0003t0004g0053 a0001c0003t0004g0276 others(17): Show |
20 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1618-102G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44320097 |