Item | Value |
---|---|
geneid | 8140 |
ensemblid | ENSG00000103257.9 |
hgncid | 11063 |
symbol | SLC7A5 |
name | solute carrier family 7 member 5 |
refseq_nuc | NM_003486.7 |
refseq_prot | NP_003477.4 |
ensembl_nuc | ENST00000261622.5 |
ensembl_prot | ENSP00000261622.4 |
mane_status | MANE Select |
chr | chr16 |
start | 87830023 |
end | 87869507 |
strand | - |
ver | v1.2 |
region | chr16:87830023-87869507 |
region5000 | chr16:87825023-87874507 |
regionname0 | SLC7A5_chr16_87830023_87869507 |
regionname5000 | SLC7A5_chr16_87825023_87874507 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 507 | 375 | 83 | 78 | 146 | 18 | 48 | 100 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | MAGAG others(502): Show |
chr16 | 87825023 | 87874507 |
a0002 | 0/0 | 507 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | MAGAG others(502): Show |
chr16 | 87825023 | 87874507 |
a0003 | 0/0 | 507 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | MAGAG others(502): Show |
chr16 | 87825023 | 87874507 |
a0004 | 0/0 | 507 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | MAGAG others(502): Show |
chr16 | 87825023 | 87874507 |
a0005 | 0/0 | 507 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | MAGAG others(502): Show |
chr16 | 87825023 | 87874507 |
a0006 | 0/0 | 507 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | MAGAG others(502): Show |
chr16 | 87825023 | 87874507 |
a0007 | 0/0 | 507 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | MAGAG others(502): Show |
chr16 | 87825023 | 87874507 |
a0008 | 0/0 | 507 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | MAGAG others(502): Show |
chr16 | 87825023 | 87874507 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1521 | 313 | 47 | 62 | 144 | 15 | 44 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0001c0002 | 0/1 | 1521 | 48 | 34 | 7 | 0 | 3 | 3 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0001c0003 | 0/0 | 1521 | 9 | 0 | 7 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0001c0005 | 0/0 | 1521 | 3 | 2 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0001c0011 | 0/0 | 1521 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0001c0013 | 0/0 | 1521 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0002c0004 | 0/0 | 1521 | 4 | 4 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0002c0016 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0003c0008 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0003c0014 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0003c0015 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0004c0006 | 0/0 | 1521 | 3 | 3 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0005c0012 | 0/0 | 1521 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0006c0007 | 0/0 | 1521 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0007c0009 | 0/0 | 1521 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 | ||
a0008c0010 | 0/0 | 1521 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ATGGC others(1516): Show |
chr16 | 87825023 | 87874507 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4559 | 76 | 2 | 13 | 55 | 1 | 5 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0002 | 1/0 | 4556 | 44 | 3 | 16 | 13 | 4 | 7 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0003 | 0/0 | 4555 | 22 | 1 | 2 | 12 | 0 | 7 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0004 | 0/0 | 4555 | 21 | 0 | 4 | 14 | 1 | 2 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0005 | 0/0 | 4555 | 18 | 1 | 4 | 8 | 2 | 3 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0006 | 0/0 | 4556 | 10 | 5 | 0 | 2 | 0 | 3 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0007 | 0/0 | 4556 | 12 | 0 | 1 | 3 | 3 | 5 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0008 | 0/0 | 4559 | 4 | 3 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0009 | 0/0 | 4559 | 9 | 0 | 0 | 9 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0010 | 0/0 | 4555 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0011 | 0/0 | 4559 | 7 | 0 | 2 | 3 | 1 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0012 | 0/0 | 4557 | 4 | 1 | 2 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0013 | 0/0 | 4555 | 5 | 0 | 0 | 0 | 1 | 4 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0014 | 0/0 | 4556 | 5 | 5 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0015 | 0/0 | 4557 | 6 | 0 | 0 | 6 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0016 | 0/0 | 4559 | 5 | 5 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0017 | 0/0 | 4557 | 5 | 5 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0018 | 0/0 | 4556 | 4 | 0 | 4 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0020 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0021 | 0/0 | 4556 | 3 | 0 | 0 | 3 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0022 | 0/0 | 4559 | 3 | 0 | 2 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0023 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0024 | 0/0 | 4555 | 3 | 3 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0025 | 0/0 | 4555 | 3 | 0 | 1 | 1 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0026 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0028 | 0/0 | 4559 | 2 | 0 | 2 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0029 | 0/0 | 4559 | 2 | 0 | 2 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0030 | 0/0 | 4559 | 2 | 1 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0032 | 0/0 | 4555 | 2 | 0 | 0 | 0 | 1 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0033 | 0/0 | 4559 | 2 | 0 | 0 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0034 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0036 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0037 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0038 | 0/0 | 4556 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0040 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0046 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0047 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0048 | 0/0 | 4555 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0049 | 0/0 | 4557 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0050 | 0/0 | 4556 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0051 | 0/0 | 4556 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0052 | 0/0 | 4556 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0053 | 0/0 | 4556 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0054 | 0/0 | 4552 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4547): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0056 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0057 | 0/0 | 4557 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0058 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0059 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0060 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0061 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0062 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0065 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0067 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0068 | 0/0 | 4568 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4563): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0069 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0070 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0071 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0072 | 0/0 | 4556 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0001t0073 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0001 | 0/0 | 4559 | 10 | 2 | 5 | 0 | 3 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0002 | 0/1 | 4556 | 3 | 0 | 1 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0005 | 0/0 | 4555 | 2 | 1 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0006 | 0/0 | 4556 | 8 | 8 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0008 | 0/0 | 4559 | 4 | 4 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0010 | 0/0 | 4555 | 6 | 5 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0012 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0013 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4550): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0016 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0020 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0023 | 0/0 | 4556 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0026 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0027 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0039 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0041 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0045 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0055 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0001c0002t0066 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0003t0001 | 0/0 | 4559 | 9 | 0 | 7 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0005t0031 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0005t0063 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0011t0001 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0001c0013t0012 | 0/0 | 4557 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0002c0004t0019 | 0/0 | 4557 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0002c0004t0043 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0002c0004t0044 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0002c0016t0019 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4552): Show |
chr16 | 87825023 | 87874507 |
a0003c0008t0064 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0003c0014t0035 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0003c0015t0042 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0004c0006t0008 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0004c0006t0014 | 0/0 | 4556 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0005c0012t0002 | 0/0 | 4556 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4551): Show |
chr16 | 87825023 | 87874507 |
a0006c0007t0001 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0007c0009t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
a0008c0010t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | ACGCA others(4554): Show |
chr16 | 87825023 | 87874507 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0003g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0006g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0007g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0007g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0007g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0007g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0007g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0007g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0007g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0007g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0007g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0007g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0007g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0007g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0008g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0008g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0009g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0009g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0009g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0009g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0009g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0009g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0009g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0010g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0010g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0011g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0011g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0011g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0011g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0011g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0011g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0011g0374 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0012g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0012g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0012g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0012g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0013g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0013g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0013g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0013g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0013g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0014g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0014g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0014g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0014g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0015g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0015g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0015g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0015g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0015g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0015g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0016g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0016g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0016g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0016g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0016g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0017g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0017g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0017g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0017g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0017g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0018g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0018g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0018g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0018g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0020g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0021g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0021g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0021g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0022g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0022g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0022g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0023g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0024g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0024g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0024g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0025g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0025g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0025g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0026g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0028g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0028g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0029g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0029g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0030g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0030g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0032g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0032g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0033g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0033g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0034g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0036g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0037g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0038g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0040g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0046g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0047g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0048g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0049g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0050g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0051g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0052g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0053g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0054g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0056g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0057g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0058g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0059g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0060g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0061g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0062g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0065g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0067g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0068g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0069g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0070g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0071g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0072g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0001t0073g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0002g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0010g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0012g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0013g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0016g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0020g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0020g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0023g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0023g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0026g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0027g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0027g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0039g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0041g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0045g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0055g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0002t0066g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0003t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0005t0031g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0005t0031g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0005t0063g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0011t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0001c0013t0012g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0002c0004t0019g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0002c0004t0019g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0002c0004t0043g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0002c0004t0044g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0002c0016t0019g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0003c0008t0064g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0003c0014t0035g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0003c0015t0042g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0004c0006t0008g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0004c0006t0008g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0004c0006t0014g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0005c0012t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0006c0007t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0007c0009t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
a0008c0010t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0021 | EUR | GBR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0178 | EUR | GBR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0016 | EUR | GBR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0274 | EUR | GBR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0283 | EUR | FIN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0282 | EUR | FIN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0023 | EUR | FIN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00323 | hp2 | a0001 | c0001 | t0032 | g0347 | EUR | FIN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00408 | hp2 | a0001 | c0001 | t0009 | g0205 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0211 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00438 | hp2 | a0001 | c0001 | t0011 | g0373 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00597 | hp2 | a0001 | c0001 | t0021 | g0252 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00609 | hp1 | a0001 | c0001 | t0021 | g0215 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00639 | hp2 | a0001 | c0002 | t0010 | g0014 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0167 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00673 | hp2 | a0001 | c0001 | t0033 | g0377 | EAS | CHS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00733 | hp2 | a0001 | c0001 | t0038 | g0176 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00735 | hp2 | a0001 | c0001 | t0022 | g0193 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01069 | hp2 | a0001 | c0001 | t0007 | g0333 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01070 | hp1 | a0001 | c0001 | t0011 | g0324 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01070 | hp2 | a0001 | c0001 | t0018 | g0313 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01071 | hp2 | a0001 | c0001 | t0018 | g0312 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01074 | hp1 | a0001 | c0001 | t0030 | g0310 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0156 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01081 | hp2 | a0001 | c0005 | t0063 | g0379 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01106 | hp2 | a0001 | c0001 | t0050 | g0060 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01109 | hp1 | a0001 | c0001 | t0012 | g0062 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01109 | hp2 | a0001 | c0001 | t0018 | g0314 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01167 | hp1 | a0001 | c0001 | t0008 | g0147 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01167 | hp2 | a0001 | c0001 | t0026 | g0127 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0375 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0170 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01192 | hp2 | a0001 | c0001 | t0028 | g0244 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01243 | hp1 | a0001 | c0001 | t0012 | g0129 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01256 | hp1 | a0001 | c0013 | t0012 | g0166 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01256 | hp2 | a0001 | c0001 | t0029 | g0163 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01258 | hp1 | a0001 | c0001 | t0029 | g0162 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0243 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0295 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01346 | hp2 | a0001 | c0001 | t0048 | g0195 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01358 | hp1 | a0001 | c0001 | t0025 | g0325 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01358 | hp2 | a0005 | c0012 | t0002 | g0292 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0113 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01433 | hp1 | a0001 | c0001 | t0022 | g0169 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0140 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01515 | hp1 | a0001 | c0001 | t0022 | g0192 | EUR | IBS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01515 | hp2 | a0001 | c0001 | t0007 | g0343 | EUR | IBS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0171 | EUR | IBS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01516 | hp2 | a0001 | c0001 | t0011 | g0374 | EUR | IBS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0172 | EUR | IBS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01517 | hp2 | a0001 | c0001 | t0007 | g0344 | EUR | IBS | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01884 | hp2 | a0001 | c0002 | t0006 | g0026 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01891 | hp1 | a0001 | c0001 | t0016 | g0288 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01891 | hp2 | a0001 | c0002 | t0023 | g0316 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01928 | hp1 | a0001 | c0003 | t0001 | g0124 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0101 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0111 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0057 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01952 | hp2 | a0001 | c0003 | t0001 | g0141 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0074 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01981 | hp1 | a0001 | c0001 | t0060 | g0144 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0334 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02004 | hp1 | a0001 | c0003 | t0001 | g0096 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02004 | hp2 | a0001 | c0001 | t0028 | g0239 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02015 | hp2 | a0001 | c0001 | t0012 | g0270 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0214 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0286 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02055 | hp2 | a0001 | c0002 | t0039 | g0050 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0332 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02074 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02083 | hp1 | a0001 | c0001 | t0054 | g0120 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02132 | hp1 | a0001 | c0001 | t0070 | g0366 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02145 | hp1 | a0001 | c0002 | t0027 | g0018 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02145 | hp2 | a0001 | c0001 | t0023 | g0351 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0368 | EAS | CDX | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | CDX | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0369 | EAS | CDX | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02257 | hp1 | a0001 | c0001 | t0030 | g0311 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0063 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02258 | hp2 | a0001 | c0001 | t0020 | g0226 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02273 | hp1 | a0001 | c0003 | t0001 | g0114 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02273 | hp2 | a0001 | c0001 | t0018 | g0315 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02280 | hp1 | a0001 | c0002 | t0006 | g0027 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0132 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02293 | hp1 | a0001 | c0001 | t0011 | g0330 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02293 | hp2 | a0006 | c0007 | t0001 | g0010 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02451 | hp1 | a0003 | c0015 | t0042 | g0059 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02451 | hp2 | a0001 | c0001 | t0016 | g0284 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02572 | hp1 | a0001 | c0002 | t0026 | g0017 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02572 | hp2 | a0001 | c0001 | t0016 | g0303 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02602 | hp1 | a0001 | c0001 | t0011 | g0322 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02615 | hp1 | a0001 | c0002 | t0020 | g0031 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02615 | hp2 | a0004 | c0006 | t0008 | g0308 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02622 | hp1 | a0001 | c0001 | t0062 | g0352 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02622 | hp2 | a0004 | c0006 | t0014 | g0307 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02630 | hp1 | a0001 | c0002 | t0010 | g0042 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02630 | hp2 | a0002 | c0004 | t0044 | g0045 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02647 | hp1 | a0001 | c0002 | t0016 | g0034 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02647 | hp2 | a0001 | c0001 | t0037 | g0118 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0354 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02717 | hp1 | a0001 | c0002 | t0010 | g0049 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0357 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02723 | hp2 | a0001 | c0001 | t0024 | g0355 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0025 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02738 | hp1 | a0001 | c0001 | t0013 | g0160 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02809 | hp1 | a0004 | c0006 | t0008 | g0309 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02809 | hp2 | a0001 | c0001 | t0024 | g0361 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02818 | hp1 | a0002 | c0004 | t0043 | g0047 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02818 | hp2 | a0001 | c0001 | t0010 | g0287 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02886 | hp1 | a0001 | c0002 | t0010 | g0036 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02886 | hp2 | a0001 | c0001 | t0012 | g0061 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02897 | hp1 | a0001 | c0002 | t0010 | g0041 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02897 | hp2 | a0001 | c0001 | t0014 | g0249 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02922 | hp1 | a0001 | c0002 | t0008 | g0020 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02922 | hp2 | a0001 | c0002 | t0041 | g0038 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02965 | hp1 | a0001 | c0001 | t0067 | g0323 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0130 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02970 | hp1 | a0002 | c0016 | t0019 | g0251 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02970 | hp2 | a0001 | c0005 | t0031 | g0378 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02976 | hp1 | a0001 | c0002 | t0006 | g0030 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0131 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03017 | hp1 | a0001 | c0011 | t0001 | g0098 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03017 | hp2 | a0001 | c0001 | t0025 | g0331 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03041 | hp1 | a0001 | c0001 | t0017 | g0217 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03041 | hp2 | a0001 | c0002 | t0010 | g0043 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03098 | hp1 | a0001 | c0002 | t0012 | g0052 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03098 | hp2 | a0001 | c0002 | t0006 | g0029 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0297 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03139 | hp2 | a0001 | c0001 | t0024 | g0356 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03195 | hp1 | a0001 | c0001 | t0014 | g0250 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03195 | hp2 | a0001 | c0001 | t0017 | g0094 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03209 | hp1 | a0003 | c0014 | t0035 | g0008 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03209 | hp2 | a0001 | c0001 | t0014 | g0055 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03225 | hp1 | a0002 | c0004 | t0019 | g0046 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03225 | hp2 | a0001 | c0002 | t0055 | g0033 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03239 | hp1 | a0001 | c0001 | t0007 | g0328 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0092 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03453 | hp1 | a0001 | c0001 | t0073 | g0382 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03453 | hp2 | a0001 | c0001 | t0017 | g0306 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03491 | hp1 | a0001 | c0001 | t0007 | g0342 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03491 | hp2 | a0001 | c0001 | t0069 | g0321 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03492 | hp2 | a0001 | c0001 | t0007 | g0341 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03516 | hp1 | a0001 | c0002 | t0005 | g0012 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03516 | hp2 | a0001 | c0001 | t0017 | g0058 | AFR | ESN | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03540 | hp1 | a0001 | c0002 | t0006 | g0028 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03540 | hp2 | a0001 | c0002 | t0006 | g0048 | AFR | GWD | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03579 | hp1 | a0003 | c0008 | t0064 | g0318 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03579 | hp2 | a0001 | c0001 | t0034 | g0009 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0175 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0125 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0340 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03704 | hp1 | a0001 | c0001 | t0007 | g0320 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0095 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03710 | hp1 | a0001 | c0001 | t0072 | g0381 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03710 | hp2 | a0001 | c0001 | t0049 | g0161 | SAS | PJL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03831 | hp1 | a0001 | c0001 | t0061 | g0335 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03831 | hp2 | a0001 | c0002 | t0013 | g0011 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03834 | hp1 | a0001 | c0002 | t0005 | g0051 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0224 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03927 | hp1 | a0001 | c0001 | t0013 | g0281 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0358 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0345 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG04115 | hp2 | a0001 | c0001 | t0032 | g0346 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG04184 | hp2 | a0001 | c0001 | t0013 | g0157 | SAS | BEB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0305 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0080 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0219 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG04228 | hp1 | a0001 | c0001 | t0058 | g0194 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0329 | SAS | STU | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18522 | hp1 | a0002 | c0004 | t0019 | g0013 | AFR | YRI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18522 | hp2 | a0001 | c0002 | t0066 | g0319 | AFR | YRI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18612 | hp1 | a0001 | c0001 | t0021 | g0258 | EAS | CHB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | CHB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18747 | hp1 | a0001 | c0001 | t0007 | g0360 | EAS | CHB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | CHB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18906 | hp1 | a0001 | c0002 | t0006 | g0002 | AFR | YRI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18906 | hp2 | a0001 | c0002 | t0008 | g0040 | AFR | YRI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0363 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18944 | hp1 | a0001 | c0001 | t0025 | g0350 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18948 | hp1 | a0001 | c0001 | t0015 | g0065 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18950 | hp2 | a0001 | c0001 | t0056 | g0112 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18957 | hp1 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18957 | hp2 | a0001 | c0001 | t0047 | g0185 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18959 | hp1 | a0001 | c0001 | t0005 | g0158 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18959 | hp2 | a0001 | c0001 | t0009 | g0119 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0367 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18964 | hp1 | a0001 | c0001 | t0015 | g0204 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18966 | hp1 | a0001 | c0001 | t0015 | g0067 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18966 | hp2 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18970 | hp2 | a0001 | c0001 | t0009 | g0107 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0364 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18975 | hp2 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18980 | hp2 | a0001 | c0001 | t0009 | g0291 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18982 | hp2 | a0001 | c0001 | t0006 | g0269 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18983 | hp2 | a0001 | c0001 | t0007 | g0339 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18986 | hp2 | a0001 | c0001 | t0059 | g0212 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18988 | hp1 | a0001 | c0001 | t0009 | g0082 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18989 | hp2 | a0001 | c0001 | t0009 | g0222 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18998 | hp1 | a0001 | c0001 | t0052 | g0089 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0362 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19002 | hp2 | a0001 | c0001 | t0057 | g0228 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19003 | hp1 | a0001 | c0001 | t0009 | g0209 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19004 | hp1 | a0001 | c0001 | t0051 | g0090 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19004 | hp2 | a0001 | c0001 | t0015 | g0066 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19005 | hp1 | a0001 | c0001 | t0071 | g0338 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19007 | hp1 | a0001 | c0001 | t0053 | g0081 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19007 | hp2 | a0001 | c0001 | t0011 | g0372 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19009 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19030 | hp1 | a0001 | c0001 | t0017 | g0117 | AFR | LWK | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0266 | AFR | LWK | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19043 | hp1 | a0001 | c0002 | t0008 | g0044 | AFR | LWK | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19043 | hp2 | a0001 | c0002 | t0023 | g0317 | AFR | LWK | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19060 | hp2 | a0001 | c0001 | t0046 | g0109 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19063 | hp1 | a0001 | c0001 | t0015 | g0152 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19064 | hp1 | a0001 | c0001 | t0015 | g0199 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19064 | hp2 | a0001 | c0001 | t0007 | g0349 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19066 | hp1 | a0001 | c0001 | t0011 | g0365 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19066 | hp2 | a0001 | c0001 | t0009 | g0208 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19067 | hp1 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19070 | hp2 | a0001 | c0001 | t0009 | g0181 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0370 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19074 | hp2 | a0007 | c0009 | t0001 | g0198 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19081 | hp2 | a0008 | c0010 | t0001 | g0210 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19088 | hp1 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19090 | hp1 | a0001 | c0001 | t0068 | g0376 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19091 | hp1 | a0001 | c0001 | t0033 | g0353 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19240 | hp1 | a0001 | c0002 | t0027 | g0019 | AFR | YRI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA19240 | hp2 | a0001 | c0005 | t0031 | g0380 | AFR | YRI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA20129 | hp1 | a0001 | c0002 | t0045 | g0035 | AFR | ASW | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA20129 | hp2 | a0001 | c0002 | t0008 | g0039 | AFR | ASW | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA20752 | hp1 | a0001 | c0001 | t0007 | g0327 | EUR | TSI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA20752 | hp2 | a0001 | c0001 | t0013 | g0277 | EUR | TSI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0201 | EUR | TSI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0121 | EUR | TSI | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA20905 | hp1 | a0001 | c0001 | t0007 | g0326 | SAS | GIH | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA20905 | hp2 | a0001 | c0001 | t0013 | g0218 | SAS | GIH | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02109 | hp1 | a0001 | c0001 | t0008 | g0145 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0165 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02486 | hp1 | a0001 | c0002 | t0006 | g0002 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0146 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG02559 | hp2 | a0001 | c0002 | t0020 | g0032 | AFR | ACB | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03471 | hp1 | a0001 | c0001 | t0014 | g0248 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG03471 | hp2 | a0001 | c0001 | t0040 | g0164 | AFR | MSL | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG06807 | hp1 | a0001 | c0001 | t0014 | g0247 | AFR | USA | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | USA | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA20300 | hp1 | a0001 | c0001 | t0016 | g0285 | AFR | USA | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | USA | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA21309 | hp1 | a0001 | c0001 | t0036 | g0064 | AFR | LWK | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
NA21309 | hp2 | a0001 | c0001 | t0065 | g0371 | AFR | LWK | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0053 | REF | REF | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0271 | REF | REF | SLC7A5_chr16_87825023_87874507 | SLC7A5 | chr16 | 87825023 | 87874507 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:87834456 | C | A | 1 | a0005 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.1426G>T | p.Val476Phe | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/10 | 1511/4556 | 1426/1524 | 476/507 | chr16 | 87834456 | |||
chr16:87836614 | C | T | 1 | a0008 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.1174G>A | p.Asp392Asn | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/10 | 1259/4556 | 1174/1524 | 392/507 | chr16 | 87836614 | |||
chr16:87841130 | G | C | 1 | a0003 | 3 | HG02451.hp1 HG03209.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.690C>G | p.Asn230Lys | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/10 | 775/4556 | 690/1524 | 230/507 | chr16 | 87841130 | |||
chr16:87841152 | T | A | 1 | a0002 | 5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.668A>T | p.Asp223Val | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/10 | 753/4556 | 668/1524 | 223/507 | chr16 | 87841152 | |||
chr16:87851804 | C | T | 1 | a0007 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.584G>A | p.Arg195Gln | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/10 | 669/4556 | 584/1524 | 195/507 | chr16 | 87851804 | |||
chr16:87869155 | C | T | 1 | a0006 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.268G>A | p.Ala90Thr | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | 353/4556 | 268/1524 | 90/507 | chr16 | 87869155 | |||
chr16:87869406 | G | A | 1 | a0004 | 3 | HG02615.hp2 HG02622.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.17C>T | p.Pro6Leu | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | 102/4556 | 17/1524 | 6/507 | chr16 | 87869406 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:87833024 | G | A | 1 | a0001c0011 | 1 | HG03017.hp1 | splice_region_variant&synonymous_variant | LOW | c.1470C>T | p.Phe490Phe | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1555/4556 | 1470/1524 | 490/507 | chr16 | 87833024 | |||
chr16:87834535 | G | C | 1 | a0001c0003 | 9 | HG01261.hp2 HG01496.hp1 HG01928.hp1 others(6): Show |
synonymous_variant | LOW | c.1347C>G | p.Val449Val | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/10 | 1432/4556 | 1347/1524 | 449/507 | chr16 | 87834535 | |||
chr16:87837854 | G | A | 1 | a0001c0013 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.1131C>T | p.Leu377Leu | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/10 | 1216/4556 | 1131/1524 | 377/507 | chr16 | 87837854 | |||
chr16:87838749 | G | A | 2 | a0003c0008 a0003c0015 |
2 | HG02451.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.1008C>T | p.Phe336Phe | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/10 | 1093/4556 | 1008/1524 | 336/507 | chr16 | 87838749 | |||
chr16:87869036 | G | A | 1 | a0001c0005 | 3 | HG01081.hp2 HG02970.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.387C>T | p.Ala129Ala | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | 472/4556 | 387/1524 | 129/507 | chr16 | 87869036 | |||
chr16:87869078 | G | T | 4 | a0001c0002 a0002c0004 a0003c0008 others(1): Show |
55 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(52): Show |
synonymous_variant | LOW | c.345C>A | p.Gly115Gly | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | 430/4556 | 345/1524 | 115/507 | chr16 | 87869078 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:87830134 | C | T | 7 | a0001c0001t0008 a0001c0002t0008 a0001c0002t0066 others(4): Show |
15 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2836G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2836 | chr16 | 87830134 | ||||||
chr16:87830196 | G | A | 1 | a0001c0001t0047 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2774C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2774 | chr16 | 87830196 | ||||||
chr16:87830236 | T | C | 1 | a0001c0001t0053 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2734A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2734 | chr16 | 87830236 | ||||||
chr16:87830334 | C | G | 1 | a0001c0001t0038 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2636G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2636 | chr16 | 87830334 | ||||||
chr16:87830396 | A | T | 1 | a0001c0001t0061 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2574T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2574 | chr16 | 87830396 | ||||||
chr16:87830468 | A | G | 18 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0017 others(15): Show |
44 | HG00733.hp2 HG01884.hp2 HG01891.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2502T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2502 | chr16 | 87830468 | ||||||
chr16:87830597 | T | C | 1 | a0001c0001t0068 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2373A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2373 | chr16 | 87830597 | ||||||
chr16:87830663 | G | A | 5 | a0001c0001t0005 a0001c0001t0025 a0001c0001t0054 others(2): Show |
25 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2307C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2307 | chr16 | 87830663 | ||||||
chr16:87830672 | C | A | 2 | a0002c0004t0043 a0003c0008t0064 |
2 | HG02818.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2298G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2298 | chr16 | 87830672 | ||||||
chr16:87830718 | C | T | 1 | a0002c0004t0043 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2252G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2252 | chr16 | 87830718 | ||||||
chr16:87830743 | C | A | 2 | a0001c0001t0067 a0001c0002t0027 |
3 | HG02145.hp1 HG02965.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2227G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2227 | chr16 | 87830743 | ||||||
chr16:87830812 | G | T | 9 | a0001c0001t0008 a0001c0001t0067 a0001c0002t0008 others(6): Show |
18 | HG01167.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2158C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2158 | chr16 | 87830812 | ||||||
chr16:87830826 | G | A | 1 | a0003c0008t0064 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2144C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2144 | chr16 | 87830826 | ||||||
chr16:87830869 | G | C | 42 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0011 others(39): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*2101C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2101 | chr16 | 87830869 | ||||||
chr16:87830877 | G | A | 12 | a0001c0001t0008 a0001c0001t0020 a0001c0001t0026 others(9): Show |
21 | HG01081.hp2 HG01167.hp1 HG01167.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2093C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2093 | chr16 | 87830877 | ||||||
chr16:87830877 | G | T | 1 | a0001c0001t0052 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2093 | chr16 | 87830877 | ||||||
chr16:87830938 | C | T | 1 | a0001c0001t0051 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2032G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2032 | chr16 | 87830938 | ||||||
chr16:87830950 | G | A | 1 | a0001c0001t0069 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2020C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 2020 | chr16 | 87830950 | ||||||
chr16:87831015 | C | T | 14 | a0001c0001t0010 a0001c0001t0020 a0001c0001t0024 others(11): Show |
23 | HG00639.hp2 HG01081.hp2 HG01167.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1955G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1955 | chr16 | 87831015 | ||||||
chr16:87831048 | C | T | 1 | a0001c0001t0058 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1922G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1922 | chr16 | 87831048 | ||||||
chr16:87831060 | C | T | 1 | a0001c0001t0046 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1910G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1910 | chr16 | 87831060 | ||||||
chr16:87831075 | C | A | 1 | a0001c0001t0028 | 2 | HG01192.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1895G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1895 | chr16 | 87831075 | ||||||
chr16:87831090 | C | T | 1 | a0001c0001t0021 | 3 | HG00597.hp2 HG00609.hp1 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1880G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1880 | chr16 | 87831090 | ||||||
chr16:87831145 | A | C | 1 | a0001c0001t0068 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1825T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1825 | chr16 | 87831145 | ||||||
chr16:87831145 | AAC | A | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(15): Show |
97 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1823_*1824delGT | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1823 | chr16 | 87831145 | ||||||
chr16:87831192 | G | A | 1 | a0003c0008t0064 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1778C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1778 | chr16 | 87831192 | ||||||
chr16:87831196 | G | A | 2 | a0001c0001t0029 a0001c0001t0070 |
3 | HG01256.hp2 HG01258.hp1 HG02132.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1774C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1774 | chr16 | 87831196 | ||||||
chr16:87831233 | G | A | 1 | a0001c0001t0059 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1737C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1737 | chr16 | 87831233 | ||||||
chr16:87831243 | C | T | 1 | a0001c0001t0022 | 3 | HG00735.hp2 HG01433.hp1 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1727G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1727 | chr16 | 87831243 | ||||||
chr16:87831279 | C | A | 2 | a0002c0004t0043 a0002c0004t0044 |
2 | HG02630.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1691G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1691 | chr16 | 87831279 | ||||||
chr16:87831334 | C | T | 1 | a0001c0002t0041 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1636G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1636 | chr16 | 87831334 | ||||||
chr16:87831416 | C | T | 48 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(45): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1554G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1554 | chr16 | 87831416 | ||||||
chr16:87831428 | G | C | 1 | a0001c0001t0040 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1542C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1542 | chr16 | 87831428 | ||||||
chr16:87831433 | A | G | 2 | a0001c0001t0016 a0001c0002t0016 |
6 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1537T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1537 | chr16 | 87831433 | ||||||
chr16:87831491 | C | T | 2 | a0002c0004t0043 a0002c0004t0044 |
2 | HG02630.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1479G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1479 | chr16 | 87831491 | ||||||
chr16:87831492 | G | A | 1 | a0003c0008t0064 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1478C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1478 | chr16 | 87831492 | ||||||
chr16:87831515 | GAC | G | 29 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(26): Show |
110 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1453_*1454delGT | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1453 | chr16 | 87831515 | ||||||
chr16:87831595 | T | A | 9 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0025 others(6): Show |
34 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1375A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1375 | chr16 | 87831595 | ||||||
chr16:87831619 | G | A | 2 | a0001c0001t0065 a0003c0015t0042 |
2 | HG02451.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1351C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1351 | chr16 | 87831619 | ||||||
chr16:87831638 | C | G | 1 | a0001c0002t0055 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1332G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1332 | chr16 | 87831638 | ||||||
chr16:87831643 | C | T | 1 | a0001c0001t0050 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1327G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1327 | chr16 | 87831643 | ||||||
chr16:87831663 | C | CGGG | 71 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(68): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*1304_*1306dupCCC | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1306 | chr16 | 87831663 | ||||||
chr16:87831688 | C | T | 44 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(41): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*1282G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1282 | chr16 | 87831688 | ||||||
chr16:87831735 | T | C | 1 | a0001c0002t0041 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1235A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1235 | chr16 | 87831735 | ||||||
chr16:87831902 | A | T | 2 | a0002c0004t0043 a0002c0004t0044 |
2 | HG02630.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1068T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1068 | chr16 | 87831902 | ||||||
chr16:87831953 | G | A | 1 | a0001c0002t0055 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1017C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 1017 | chr16 | 87831953 | ||||||
chr16:87831995 | G | A | 1 | a0001c0001t0060 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*975C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 975 | chr16 | 87831995 | ||||||
chr16:87832086 | G | T | 4 | a0002c0004t0019 a0002c0004t0043 a0002c0004t0044 others(1): Show |
5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*884C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 884 | chr16 | 87832086 | ||||||
chr16:87832225 | C | T | 1 | a0001c0001t0056 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*745G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 745 | chr16 | 87832225 | ||||||
chr16:87832313 | G | A | 2 | a0001c0001t0016 a0001c0002t0016 |
6 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*657C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 657 | chr16 | 87832313 | ||||||
chr16:87832342 | G | A | 2 | a0001c0001t0071 a0001c0002t0055 |
2 | HG03225.hp2 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*628C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 628 | chr16 | 87832342 | ||||||
chr16:87832391 | C | T | 1 | a0001c0001t0018 | 4 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*579G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 579 | chr16 | 87832391 | ||||||
chr16:87832477 | C | CGAATGTC others(4): Show |
1 | a0001c0001t0068 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*482_*492dupTTGTGA others(5): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 492 | chr16 | 87832477 | ||||||
chr16:87832501 | G | T | 2 | a0001c0001t0065 a0003c0015t0042 |
2 | HG02451.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*469C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 469 | chr16 | 87832501 | ||||||
chr16:87832512 | C | T | 12 | a0001c0001t0008 a0001c0001t0026 a0001c0001t0034 others(9): Show |
20 | HG01081.hp2 HG01167.hp1 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*458G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 458 | chr16 | 87832512 | ||||||
chr16:87832532 | G | C | 26 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0011 others(23): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*438C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 438 | chr16 | 87832532 | ||||||
chr16:87832681 | A | T | 11 | a0001c0001t0006 a0001c0001t0023 a0001c0001t0037 others(8): Show |
29 | HG00733.hp2 HG01884.hp2 HG01891.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*289T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 289 | chr16 | 87832681 | ||||||
chr16:87832768 | TGG | T | 2 | a0002c0004t0019 a0002c0016t0019 |
3 | HG02970.hp1 HG03225.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*200_*201delCC | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 200 | chr16 | 87832768 | ||||||
chr16:87832894 | C | T | 1 | a0001c0001t0036 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*76G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 10/10 | 76 | chr16 | 87832894 | ||||||
chr16:87869453 | C | G | 2 | a0001c0001t0034 a0003c0014t0035 |
2 | HG03209.hp1 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-31G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | 31 | chr16 | 87869453 | ||||||
chr16:87869471 | G | A | 3 | a0001c0001t0018 a0001c0001t0030 a0001c0001t0073 |
7 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-49C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | chr16 | 87869471 | |||||||
chr16:87869471 | G | C | 1 | a0001c0001t0072 | 1 | HG03710.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-49C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | chr16 | 87869471 | |||||||
chr16:87869476 | G | C | 23 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0011 others(20): Show |
69 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(66): Show |
5_prime_UTR_variant | MODIFIER | c.-54C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/10 | 54 | chr16 | 87869476 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:87833084 | C | T | 3 | a0001c0001t0020g0226 a0001c0002t0020g0031 a0001c0002t0020g0032 |
3 | HG02258.hp2 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1469-59G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833084 | |||||||
chr16:87833128 | C | T | 1 | a0007c0009t0001g0198 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1469-103G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833128 | |||||||
chr16:87833133 | G | A | 13 | a0001c0001t0008g0145 a0001c0001t0008g0146 a0001c0001t0008g0147 others(10): Show |
13 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1469-108C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833133 | |||||||
chr16:87833138 | T | C | 1 | a0001c0001t0061g0335 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1469-113A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833138 | |||||||
chr16:87833182 | G | C | 2 | a0001c0001t0065g0371 a0003c0015t0042g0059 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1469-157C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833182 | |||||||
chr16:87833193 | C | T | 1 | a0001c0001t0030g0311 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1469-168G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833193 | |||||||
chr16:87833195 | G | A | 1 | a0001c0001t0004g0243 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1469-170C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833195 | |||||||
chr16:87833204 | A | G | 6 | a0001c0001t0026g0127 a0001c0001t0034g0009 a0001c0001t0040g0164 others(3): Show |
6 | HG01081.hp2 HG01167.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469-179T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833204 | |||||||
chr16:87833252 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1469-227G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833252 | |||||||
chr16:87833259 | C | T | 2 | a0001c0001t0002g0083 a0001c0001t0002g0084 |
2 | HG01099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1469-234G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833259 | |||||||
chr16:87833275 | C | T | 2 | a0001c0001t0003g0340 a0001c0001t0003g0345 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1469-250G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833275 | |||||||
chr16:87833291 | C | T | 3 | a0002c0004t0019g0013 a0002c0004t0019g0046 a0002c0016t0019g0251 |
3 | HG02970.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1469-266G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833291 | |||||||
chr16:87833308 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1469-283C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833308 | |||||||
chr16:87833420 | G | C | 1 | a0001c0001t0012g0129 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1469-395C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833420 | |||||||
chr16:87833424 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1469-399C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833424 | |||||||
chr16:87833463 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1469-438G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833463 | |||||||
chr16:87833509 | G | A | 17 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0086 others(14): Show |
19 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.1469-484C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833509 | |||||||
chr16:87833534 | G | A | 2 | a0001c0001t0004g0074 a0001c0001t0004g0282 |
2 | HG00280.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1469-509C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833534 | |||||||
chr16:87833540 | A | C | 5 | a0002c0004t0019g0013 a0002c0004t0019g0046 a0002c0004t0043g0047 others(2): Show |
5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469-515T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833540 | |||||||
chr16:87833618 | G | A | 15 | a0001c0001t0002g0253 a0001c0001t0002g0259 a0001c0001t0002g0260 others(12): Show |
15 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1469-593C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833618 | |||||||
chr16:87833631 | TGGGGTAG others(6): Show |
T | 40 | a0001c0001t0008g0145 a0001c0001t0008g0146 a0001c0001t0008g0147 others(37): Show |
40 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.1469-619_1469-607d others(15): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833631 | |||||||
chr16:87833642 | T | C | 19 | a0001c0001t0006g0130 a0001c0001t0006g0131 a0001c0001t0006g0132 others(16): Show |
19 | HG00733.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1469-617A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833642 | |||||||
chr16:87833724 | G | A | 1 | a0001c0001t0015g0199 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1468+690C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833724 | |||||||
chr16:87833775 | G | A | 8 | a0001c0001t0012g0061 a0001c0001t0012g0062 a0001c0001t0017g0117 others(5): Show |
8 | HG01109.hp1 HG01256.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1468+639C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833775 | |||||||
chr16:87833789 | G | C | 1 | a0001c0001t0037g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1468+625C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833789 | |||||||
chr16:87833803 | C | T | 1 | a0001c0001t0012g0129 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1468+611G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833803 | |||||||
chr16:87833818 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1468+596G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833818 | |||||||
chr16:87833841 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1468+573C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833841 | |||||||
chr16:87833857 | CT | C | 205 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(202): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1468+556delA | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833857 | |||||||
chr16:87833896 | C | T | 1 | a0001c0001t0006g0069 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1468+518G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833896 | |||||||
chr16:87833901 | T | C | 1 | a0001c0001t0003g0375 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1468+513A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833901 | |||||||
chr16:87833910 | A | G | 1 | a0001c0001t0003g0375 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1468+504T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833910 | |||||||
chr16:87833914 | T | C | 1 | a0001c0001t0003g0375 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1468+500A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833914 | |||||||
chr16:87833939 | C | T | 1 | a0001c0001t0003g0375 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1468+475G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833939 | |||||||
chr16:87833940 | G | A | 4 | a0001c0001t0006g0069 a0001c0002t0006g0002 a0001c0002t0006g0048 others(1): Show |
5 | HG02055.hp2 HG02486.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1468+474C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833940 | |||||||
chr16:87833941 | T | C | 1 | a0001c0001t0003g0375 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1468+473A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833941 | |||||||
chr16:87833985 | C | T | 93 | a0001c0001t0002g0077 a0001c0001t0002g0180 a0001c0001t0003g0007 others(90): Show |
94 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1468+429G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87833985 | |||||||
chr16:87834043 | A | G | 18 | a0001c0001t0012g0129 a0001c0001t0017g0058 a0001c0001t0017g0094 others(15): Show |
18 | HG01081.hp2 HG01167.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1468+371T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87834043 | |||||||
chr16:87834176 | G | A | 10 | a0001c0001t0012g0129 a0001c0001t0026g0127 a0001c0001t0034g0009 others(7): Show |
10 | HG01081.hp2 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1468+238C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87834176 | |||||||
chr16:87834196 | C | G | 5 | a0002c0004t0019g0013 a0002c0004t0019g0046 a0002c0004t0043g0047 others(2): Show |
5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1468+218G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87834196 | |||||||
chr16:87834266 | G | A | 141 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(138): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1468+148C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87834266 | |||||||
chr16:87834344 | G | A | 1 | a0003c0008t0064g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1468+70C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87834344 | |||||||
chr16:87834403 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1468+11C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 9/9 | chr16 | 87834403 | |||||||
chr16:87834689 | C | T | 2 | a0001c0001t0004g0095 a0001c0001t0004g0219 |
2 | HG03704.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1291-98G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87834689 | |||||||
chr16:87834747 | G | A | 1 | a0001c0001t0034g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1291-156C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87834747 | |||||||
chr16:87834856 | C | T | 35 | a0001c0001t0002g0077 a0001c0001t0002g0180 a0001c0001t0005g0063 others(32): Show |
35 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1291-265G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87834856 | |||||||
chr16:87834921 | C | A | 141 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(138): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1291-330G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87834921 | |||||||
chr16:87834991 | C | T | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1291-400G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87834991 | |||||||
chr16:87835084 | C | T | 6 | a0001c0001t0073g0382 a0002c0004t0019g0013 a0002c0004t0019g0046 others(3): Show |
6 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291-493G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835084 | |||||||
chr16:87835224 | T | C | 145 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(142): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1291-633A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835224 | |||||||
chr16:87835225 | G | A | 141 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(138): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1291-634C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835225 | |||||||
chr16:87835259 | C | A | 1 | a0001c0001t0009g0119 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1291-668G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835259 | |||||||
chr16:87835276 | G | T | 1 | a0001c0001t0001g0232 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1291-685C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835276 | |||||||
chr16:87835335 | G | A | 2 | a0001c0001t0028g0239 a0001c0001t0028g0244 |
2 | HG01192.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1291-744C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835335 | |||||||
chr16:87835342 | G | A | 5 | a0002c0004t0019g0013 a0002c0004t0019g0046 a0002c0004t0043g0047 others(2): Show |
5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291-751C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835342 | |||||||
chr16:87835342 | G | C | 162 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(159): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1291-751C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835342 | |||||||
chr16:87835368 | C | G | 153 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(150): Show |
155 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.1291-777G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835368 | |||||||
chr16:87835373 | C | T | 6 | a0001c0001t0014g0055 a0001c0001t0014g0247 a0001c0001t0014g0248 others(3): Show |
6 | HG02622.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291-782G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835373 | |||||||
chr16:87835484 | A | T | 35 | a0001c0001t0002g0077 a0001c0001t0002g0180 a0001c0001t0004g0264 others(32): Show |
35 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1291-893T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835484 | |||||||
chr16:87835503 | T | C | 1 | a0001c0001t0003g0358 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1291-912A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835503 | |||||||
chr16:87835537 | T | G | 1 | a0001c0001t0004g0101 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1291-946A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835537 | |||||||
chr16:87835547 | T | C | 6 | a0001c0001t0014g0055 a0001c0001t0014g0247 a0001c0001t0014g0248 others(3): Show |
6 | HG02622.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1290+951A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835547 | |||||||
chr16:87835566 | C | T | 14 | a0001c0001t0012g0129 a0001c0001t0020g0226 a0001c0001t0026g0127 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1290+932G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835566 | |||||||
chr16:87835574 | T | C | 1 | a0001c0001t0002g0261 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1290+924A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835574 | |||||||
chr16:87835614 | T | C | 323 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(320): Show |
329 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.1290+884A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835614 | |||||||
chr16:87835619 | G | A | 2 | a0002c0004t0043g0047 a0002c0004t0044g0045 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1290+879C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835619 | |||||||
chr16:87835623 | G | A | 1 | a0001c0013t0012g0166 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1290+875C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835623 | |||||||
chr16:87835633 | C | G | 1 | a0001c0002t0016g0034 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1290+865G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835633 | |||||||
chr16:87835663 | A | G | 2 | a0001c0001t0013g0157 a0001c0002t0013g0011 |
2 | HG03831.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1290+835T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835663 | |||||||
chr16:87835664 | C | T | 26 | a0001c0001t0002g0077 a0001c0001t0002g0180 a0001c0001t0002g0259 others(23): Show |
26 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1290+834G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835664 | |||||||
chr16:87835676 | G | A | 1 | a0001c0001t0006g0175 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1290+822C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835676 | |||||||
chr16:87835690 | G | A | 1 | a0001c0001t0006g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1290+808C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835690 | |||||||
chr16:87835695 | C | T | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1290+803G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835695 | |||||||
chr16:87835696 | T | A | 1 | a0001c0001t0002g0083 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1290+802A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835696 | |||||||
chr16:87835696 | T | G | 28 | a0001c0001t0003g0329 a0001c0001t0003g0340 a0001c0001t0005g0080 others(25): Show |
29 | HG01167.hp1 HG01891.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1290+802A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835696 | |||||||
chr16:87835707 | T | C | 163 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(160): Show |
169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1290+791A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835707 | |||||||
chr16:87835709 | T | C | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1290+789A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835709 | |||||||
chr16:87835716 | T | C | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1290+782A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835716 | |||||||
chr16:87835717 | G | A | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1290+781C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835717 | |||||||
chr16:87835721 | G | T | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1290+777C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835721 | |||||||
chr16:87835761 | A | G | 13 | a0001c0001t0003g0357 a0001c0001t0010g0266 a0001c0001t0010g0287 others(10): Show |
13 | HG00639.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1290+737T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835761 | |||||||
chr16:87835763 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1290+735G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835763 | |||||||
chr16:87835764 | G | A | 14 | a0001c0001t0003g0357 a0001c0001t0010g0266 a0001c0001t0010g0287 others(11): Show |
14 | HG00639.hp2 HG02630.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1290+734C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835764 | |||||||
chr16:87835765 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1290+733G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835765 | |||||||
chr16:87835767 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1290+731G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835767 | |||||||
chr16:87835770 | A | C | 3 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0012g0270 |
3 | HG02015.hp2 NA18950.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1290+728T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835770 | |||||||
chr16:87835770 | A | G | 71 | a0001c0001t0001g0177 a0001c0001t0001g0235 a0001c0001t0001g0273 others(68): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1290+728T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835770 | |||||||
chr16:87835788 | C | T | 1 | a0001c0001t0004g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1290+710G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835788 | |||||||
chr16:87835809 | G | C | 1 | a0001c0001t0011g0330 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1290+689C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835809 | |||||||
chr16:87835910 | C | G | 78 | a0001c0001t0002g0077 a0001c0001t0002g0180 a0001c0001t0002g0253 others(75): Show |
78 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.1290+588G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835910 | |||||||
chr16:87835934 | C | T | 47 | a0001c0001t0002g0077 a0001c0001t0002g0180 a0001c0001t0002g0253 others(44): Show |
47 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1290+564G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87835934 | |||||||
chr16:87836034 | G | A | 107 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(104): Show |
108 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.1290+464C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87836034 | |||||||
chr16:87836105 | C | T | 71 | a0001c0001t0002g0077 a0001c0001t0002g0180 a0001c0001t0002g0253 others(68): Show |
71 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1290+393G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87836105 | |||||||
chr16:87836386 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1290+112C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87836386 | |||||||
chr16:87836438 | G | A | 1 | a0003c0014t0035g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1290+60C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 8/9 | chr16 | 87836438 | |||||||
chr16:87836686 | C | T | 14 | a0001c0001t0008g0145 a0001c0001t0008g0146 a0001c0001t0008g0147 others(11): Show |
14 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1141-39G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836686 | |||||||
chr16:87836703 | G | A | 1 | a0008c0010t0001g0210 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1141-56C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836703 | |||||||
chr16:87836706 | C | T | 71 | a0001c0001t0002g0077 a0001c0001t0002g0180 a0001c0001t0002g0253 others(68): Show |
71 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1141-59G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836706 | |||||||
chr16:87836740 | G | A | 1 | a0003c0008t0064g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1141-93C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836740 | |||||||
chr16:87836773 | A | G | 71 | a0001c0001t0002g0077 a0001c0001t0002g0180 a0001c0001t0002g0253 others(68): Show |
71 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1141-126T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836773 | |||||||
chr16:87836867 | A | G | 1 | a0001c0002t0041g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1141-220T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836867 | |||||||
chr16:87836948 | T | C | 9 | a0001c0001t0001g0177 a0001c0001t0006g0130 a0001c0001t0006g0175 others(6): Show |
9 | HG00733.hp2 HG02965.hp2 HG03654.hp2 others(6): Show |
intron_variant | MODIFIER | c.1141-301A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836948 | |||||||
chr16:87836968 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1141-321G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87836968 | |||||||
chr16:87837001 | A | G | 65 | a0001c0001t0002g0077 a0001c0001t0002g0180 a0001c0001t0002g0298 others(62): Show |
65 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.1141-354T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837001 | |||||||
chr16:87837045 | C | T | 4 | a0001c0001t0065g0371 a0003c0008t0064g0318 a0003c0014t0035g0008 others(1): Show |
4 | HG02451.hp1 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-398G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837045 | |||||||
chr16:87837067 | G | A | 43 | a0001c0001t0001g0293 a0001c0001t0003g0007 a0001c0001t0003g0329 others(40): Show |
44 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.1141-420C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837067 | |||||||
chr16:87837117 | G | C | 87 | a0001c0001t0003g0007 a0001c0001t0003g0329 a0001c0001t0003g0332 others(84): Show |
89 | HG00438.hp1 HG00639.hp2 HG01167.hp1 others(86): Show |
intron_variant | MODIFIER | c.1141-470C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837117 | |||||||
chr16:87837204 | T | G | 13 | a0001c0001t0008g0145 a0001c0001t0008g0146 a0001c0001t0008g0147 others(10): Show |
13 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1141-557A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837204 | |||||||
chr16:87837260 | T | C | 315 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(312): Show |
321 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.1140+585A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837260 | |||||||
chr16:87837297 | T | TG | 73 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(70): Show |
73 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.1140+547dupC | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837297 | |||||||
chr16:87837321 | C | G | 1 | a0001c0001t0034g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1140+524G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837321 | |||||||
chr16:87837407 | T | A | 5 | a0001c0001t0017g0058 a0001c0001t0017g0094 a0001c0001t0017g0117 others(2): Show |
5 | HG03041.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140+438A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837407 | |||||||
chr16:87837490 | A | G | 73 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(70): Show |
73 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.1140+355T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837490 | |||||||
chr16:87837535 | C | T | 3 | a0001c0001t0005g0155 a0001c0001t0005g0158 a0001c0001t0005g0159 |
3 | NA18959.hp1 NA18966.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1140+310G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837535 | |||||||
chr16:87837550 | C | G | 1 | a0001c0002t0001g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1140+295G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837550 | |||||||
chr16:87837595 | G | A | 6 | a0001c0001t0011g0374 a0001c0001t0030g0310 a0001c0001t0030g0311 others(3): Show |
8 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1140+250C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837595 | |||||||
chr16:87837607 | G | A | 71 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(68): Show |
71 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1140+238C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837607 | |||||||
chr16:87837622 | G | A | 3 | a0001c0001t0005g0155 a0001c0001t0005g0158 a0001c0001t0005g0159 |
3 | NA18959.hp1 NA18966.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1140+223C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837622 | |||||||
chr16:87837637 | T | A | 1 | a0003c0014t0035g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1140+208A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837637 | |||||||
chr16:87837658 | A | G | 310 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(307): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.1140+187T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837658 | |||||||
chr16:87837734 | C | T | 27 | a0001c0001t0006g0069 a0001c0001t0006g0130 a0001c0001t0008g0145 others(24): Show |
28 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1140+111G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837734 | |||||||
chr16:87837760 | G | C | 71 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(68): Show |
71 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1140+85C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837760 | |||||||
chr16:87837797 | C | T | 4 | a0001c0001t0001g0099 a0001c0001t0001g0188 a0001c0001t0001g0191 others(1): Show |
4 | HG02027.hp2 HG02040.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140+48G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 7/9 | chr16 | 87837797 | |||||||
chr16:87837976 | G | A | 70 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(67): Show |
70 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.1044-35C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87837976 | |||||||
chr16:87838022 | G | C | 1 | a0001c0001t0062g0352 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1044-81C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838022 | |||||||
chr16:87838108 | T | G | 311 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(308): Show |
317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.1044-167A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838108 | |||||||
chr16:87838157 | C | G | 2 | a0002c0004t0043g0047 a0002c0004t0044g0045 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1044-216G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838157 | |||||||
chr16:87838215 | C | G | 1 | a0001c0001t0073g0382 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1044-274G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838215 | |||||||
chr16:87838291 | C | CT | 71 | a0001c0001t0001g0299 a0001c0001t0003g0007 a0001c0001t0003g0329 others(68): Show |
73 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(70): Show |
intron_variant | MODIFIER | c.1044-351dupA | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838291 | |||||||
chr16:87838291 | C | CTT | 6 | a0001c0001t0003g0363 a0001c0001t0004g0263 a0001c0001t0023g0351 others(3): Show |
6 | HG00438.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044-352_1044-351d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838291 | |||||||
chr16:87838291 | CT | C | 163 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(160): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1044-351delA | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838291 | |||||||
chr16:87838291 | CTTTTTT | C | 69 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(66): Show |
69 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.1044-356_1044-351d others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838291 | |||||||
chr16:87838403 | G | C | 72 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(69): Show |
72 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1043+311C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838403 | |||||||
chr16:87838433 | G | A | 4 | a0001c0001t0003g0357 a0001c0001t0024g0355 a0001c0001t0024g0356 others(1): Show |
4 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+281C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838433 | |||||||
chr16:87838482 | G | A | 4 | a0001c0001t0067g0323 a0001c0002t0027g0018 a0001c0002t0027g0019 others(1): Show |
4 | HG02145.hp1 HG02965.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+232C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838482 | |||||||
chr16:87838708 | G | A | 13 | a0001c0001t0008g0145 a0001c0001t0008g0146 a0001c0001t0008g0147 others(10): Show |
13 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1043+6C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 6/9 | chr16 | 87838708 | |||||||
chr16:87838882 | G | A | 71 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(68): Show |
71 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.940-65C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87838882 | |||||||
chr16:87839010 | C | G | 1 | a0001c0001t0017g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.940-193G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839010 | |||||||
chr16:87839057 | T | A | 1 | a0001c0001t0034g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.940-240A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839057 | |||||||
chr16:87839111 | C | G | 2 | a0002c0004t0043g0047 a0002c0004t0044g0045 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.940-294G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839111 | |||||||
chr16:87839112 | G | C | 325 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(322): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.940-295C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839112 | |||||||
chr16:87839136 | C | T | 2 | a0002c0004t0043g0047 a0002c0004t0044g0045 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.940-319G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839136 | |||||||
chr16:87839137 | G | A | 40 | a0001c0001t0003g0007 a0001c0001t0003g0329 a0001c0001t0003g0332 others(37): Show |
41 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.940-320C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839137 | |||||||
chr16:87839147 | C | T | 2 | a0001c0001t0005g0063 a0001c0002t0005g0012 |
2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.940-330G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839147 | |||||||
chr16:87839238 | A | G | 324 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(321): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.940-421T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839238 | |||||||
chr16:87839245 | G | A | 7 | a0001c0001t0006g0069 a0001c0001t0067g0323 a0001c0002t0006g0002 others(4): Show |
8 | HG02055.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.940-428C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839245 | |||||||
chr16:87839250 | C | A | 4 | a0001c0001t0006g0069 a0001c0002t0006g0002 a0001c0002t0006g0048 others(1): Show |
5 | HG02055.hp2 HG02486.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-433G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839250 | |||||||
chr16:87839338 | C | T | 1 | a0001c0001t0009g0205 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.939+364G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839338 | |||||||
chr16:87839430 | G | A | 3 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0011g0324 |
3 | HG00140.hp2 HG00738.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.939+272C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839430 | |||||||
chr16:87839526 | C | T | 50 | a0001c0001t0003g0007 a0001c0001t0003g0329 a0001c0001t0003g0332 others(47): Show |
51 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.939+176G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839526 | |||||||
chr16:87839584 | G | A | 2 | a0002c0004t0043g0047 a0002c0004t0044g0045 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.939+118C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839584 | |||||||
chr16:87839614 | G | A | 1 | a0001c0001t0034g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.939+88C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839614 | |||||||
chr16:87839641 | A | C | 217 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(214): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.939+61T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 5/9 | chr16 | 87839641 | |||||||
chr16:87839830 | A | G | 1 | a0001c0001t0011g0365 | 1 | NA19066.hp1 | splice_region_variant&intron_variant | LOW | c.816-5T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839830 | |||||||
chr16:87839836 | C | G | 3 | a0001c0001t0002g0179 a0001c0001t0007g0326 a0001c0001t0007g0327 |
3 | HG01106.hp1 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.816-11G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839836 | |||||||
chr16:87839865 | G | A | 40 | a0001c0001t0003g0007 a0001c0001t0003g0329 a0001c0001t0003g0332 others(37): Show |
41 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.816-40C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839865 | |||||||
chr16:87839914 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.816-89C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839914 | |||||||
chr16:87839918 | T | G | 1 | a0001c0002t0001g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.816-93A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839918 | |||||||
chr16:87839971 | A | G | 79 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(76): Show |
80 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.816-146T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839971 | |||||||
chr16:87839983 | G | C | 1 | a0001c0001t0004g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.816-158C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839983 | |||||||
chr16:87839991 | G | C | 13 | a0001c0001t0008g0145 a0001c0001t0008g0146 a0001c0001t0008g0147 others(10): Show |
13 | HG01167.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.816-166C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87839991 | |||||||
chr16:87840026 | T | C | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.816-201A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87840026 | |||||||
chr16:87840146 | G | A | 3 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0003c0008t0064g0318 |
3 | HG03579.hp1 NA18950.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.815+283C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87840146 | |||||||
chr16:87840320 | G | T | 1 | a0003c0008t0064g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.815+109C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 4/9 | chr16 | 87840320 | |||||||
chr16:87840501 | TATATG | T | 70 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(67): Show |
70 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.771-33_771-29delCA others(3): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840501 | |||||||
chr16:87840534 | G | A | 39 | a0001c0001t0003g0007 a0001c0001t0003g0329 a0001c0001t0003g0332 others(36): Show |
40 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.771-61C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840534 | |||||||
chr16:87840576 | T | C | 70 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(67): Show |
70 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.771-103A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840576 | |||||||
chr16:87840600 | C | T | 8 | a0001c0001t0001g0177 a0001c0001t0006g0175 a0001c0001t0006g0223 others(5): Show |
8 | HG00733.hp2 HG03654.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.771-127G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840600 | |||||||
chr16:87840611 | TGGGA | T | 70 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(67): Show |
70 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.771-142_771-139del others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840611 | |||||||
chr16:87840633 | C | T | 2 | a0003c0008t0064g0318 a0003c0014t0035g0008 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.771-160G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840633 | |||||||
chr16:87840640 | C | T | 10 | a0001c0001t0006g0131 a0001c0001t0006g0132 a0001c0001t0006g0165 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.771-167G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840640 | |||||||
chr16:87840723 | G | A | 1 | a0001c0001t0016g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.771-250C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840723 | |||||||
chr16:87840730 | G | A | 70 | a0001c0001t0001g0177 a0001c0001t0002g0077 a0001c0001t0002g0180 others(67): Show |
70 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.771-257C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840730 | |||||||
chr16:87840786 | C | T | 2 | a0001c0002t0027g0018 a0001c0002t0027g0019 |
2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.770+264G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840786 | |||||||
chr16:87840787 | G | A | 1 | a0001c0001t0004g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.770+263C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840787 | |||||||
chr16:87840817 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0003g0354 |
2 | HG01243.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.770+233C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840817 | |||||||
chr16:87840820 | G | A | 38 | a0001c0001t0003g0007 a0001c0001t0003g0329 a0001c0001t0003g0332 others(35): Show |
39 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.770+230C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840820 | |||||||
chr16:87840907 | TCTTTAAC others(37): Show |
T | 2 | a0001c0001t0006g0130 a0001c0001t0034g0009 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.770+99_770+142delG others(43): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840907 | |||||||
chr16:87840943 | G | A | 1 | a0001c0001t0070g0366 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.770+107C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 3/9 | chr16 | 87840943 | |||||||
chr16:87841250 | A | G | 10 | a0001c0001t0006g0069 a0001c0002t0006g0002 a0001c0002t0006g0048 others(7): Show |
11 | HG02055.hp2 HG02486.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.665-95T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841250 | |||||||
chr16:87841292 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.665-137C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841292 | |||||||
chr16:87841347 | A | G | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665-192T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841347 | |||||||
chr16:87841502 | G | A | 1 | a0001c0001t0018g0315 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.665-347C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841502 | |||||||
chr16:87841557 | C | A | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665-402G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841557 | |||||||
chr16:87841558 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.665-403C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841558 | |||||||
chr16:87841623 | C | T | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665-468G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841623 | |||||||
chr16:87841678 | T | C | 20 | a0001c0001t0006g0131 a0001c0001t0006g0132 a0001c0001t0014g0055 others(17): Show |
20 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.665-523A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841678 | |||||||
chr16:87841794 | C | T | 1 | a0001c0001t0009g0107 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.665-639G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841794 | |||||||
chr16:87841797 | G | A | 2 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.665-642C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841797 | |||||||
chr16:87841893 | T | C | 2 | a0001c0001t0003g0357 a0003c0008t0064g0318 |
2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.665-738A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87841893 | |||||||
chr16:87842102 | AAAG | A | 3 | a0001c0001t0013g0281 a0001c0001t0032g0346 a0001c0001t0032g0347 |
3 | HG00323.hp2 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.665-950_665-948del others(3): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842102 | |||||||
chr16:87842272 | C | T | 1 | a0003c0014t0035g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.665-1117G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842272 | |||||||
chr16:87842312 | G | T | 1 | a0001c0001t0003g0363 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-1157C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842312 | |||||||
chr16:87842313 | T | G | 1 | a0001c0001t0003g0363 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-1158A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842313 | |||||||
chr16:87842324 | G | A | 1 | a0001c0002t0020g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665-1169C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842324 | |||||||
chr16:87842403 | G | A | 1 | a0001c0001t0003g0337 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.665-1248C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842403 | |||||||
chr16:87842520 | C | A | 8 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0273 others(5): Show |
8 | HG00140.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.665-1365G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842520 | |||||||
chr16:87842558 | T | C | 22 | a0001c0001t0006g0069 a0001c0001t0006g0130 a0001c0001t0006g0131 others(19): Show |
23 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.665-1403A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842558 | |||||||
chr16:87842569 | C | T | 155 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(152): Show |
159 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.665-1414G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842569 | |||||||
chr16:87842666 | G | C | 2 | a0001c0001t0029g0162 a0001c0001t0029g0163 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.665-1511C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842666 | |||||||
chr16:87842696 | C | T | 1 | a0003c0008t0064g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.665-1541G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842696 | |||||||
chr16:87842769 | T | C | 140 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(137): Show |
141 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.665-1614A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842769 | |||||||
chr16:87842777 | CCAGGTGG others(4): Show |
C | 1 | a0001c0002t0010g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.665-1633_665-1623d others(13): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842777 | |||||||
chr16:87842868 | G | A | 1 | a0001c0001t0004g0095 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.665-1713C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842868 | |||||||
chr16:87842869 | G | GCCAAGAC others(3): Show |
316 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(313): Show |
322 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.665-1715_665-1714i others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842869 | |||||||
chr16:87842869 | G | GCCAAGAT others(3): Show |
1 | a0003c0014t0035g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.665-1715_665-1714i others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842869 | |||||||
chr16:87842894 | A | G | 123 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(120): Show |
124 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.665-1739T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842894 | |||||||
chr16:87842935 | C | T | 3 | a0001c0001t0022g0169 a0001c0001t0022g0192 a0001c0001t0022g0193 |
3 | HG00735.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.665-1780G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842935 | |||||||
chr16:87842961 | C | T | 133 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(130): Show |
134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.665-1806G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87842961 | |||||||
chr16:87843025 | C | A | 134 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(131): Show |
135 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.665-1870G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843025 | |||||||
chr16:87843109 | G | A | 1 | a0001c0001t0003g0363 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-1954C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843109 | |||||||
chr16:87843206 | T | C | 135 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(132): Show |
136 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.665-2051A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843206 | |||||||
chr16:87843214 | A | G | 1 | a0001c0001t0001g0294 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.665-2059T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843214 | |||||||
chr16:87843226 | G | C | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665-2071C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843226 | |||||||
chr16:87843253 | T | C | 322 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(319): Show |
328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.665-2098A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843253 | |||||||
chr16:87843292 | T | C | 1 | a0001c0002t0041g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.665-2137A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843292 | |||||||
chr16:87843347 | C | CT | 11 | a0001c0001t0001g0071 a0001c0001t0001g0273 a0001c0001t0001g0274 others(8): Show |
11 | HG00140.hp2 HG00738.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.665-2193dupA | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CT | C | 7 | a0001c0001t0002g0137 a0001c0001t0002g0179 a0001c0001t0002g0206 others(4): Show |
7 | HG01070.hp1 HG01106.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.665-2193delA | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CTTTTTTT | C | 18 | a0001c0001t0006g0069 a0001c0001t0006g0132 a0001c0001t0014g0055 others(15): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.665-2199_665-2193d others(9): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CTTTTTTT others(1): Show |
C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0154 others(23): Show |
27 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.665-2200_665-2193d others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CTTTTTTT others(2): Show |
C | 108 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0068 others(105): Show |
111 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.665-2201_665-2193d others(11): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CTTTTTTT others(3): Show |
C | 20 | a0001c0001t0001g0150 a0001c0001t0001g0240 a0001c0001t0001g0242 others(17): Show |
20 | HG00323.hp1 HG00408.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.665-2202_665-2193d others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0006g0130 a0001c0001t0033g0353 |
2 | HG02965.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.665-2203_665-2193d others(13): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CTTTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0072 a0001c0001t0003g0364 a0001c0001t0003g0368 others(5): Show |
8 | HG01346.hp1 HG02109.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.665-2204_665-2193d others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CTTTTTTT others(6): Show |
C | 40 | a0001c0001t0001g0265 a0001c0001t0003g0007 a0001c0001t0003g0329 others(37): Show |
41 | HG00438.hp1 HG00639.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.665-2205_665-2193d others(15): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CTTTTTTT others(7): Show |
C | 73 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0002g0084 others(70): Show |
73 | HG00423.hp2 HG00642.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.665-2206_665-2193d others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CTTTTTTT others(8): Show |
C | 14 | a0001c0001t0002g0077 a0001c0001t0003g0363 a0001c0001t0008g0145 others(11): Show |
14 | HG00323.hp2 HG01123.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.665-2207_665-2193d others(17): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0008g0147 a0001c0002t0008g0039 |
2 | HG01167.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.665-2208_665-2193d others(18): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CTTTTTTT others(15): Show |
C | 5 | a0001c0001t0001g0085 a0001c0001t0003g0340 a0001c0001t0003g0345 others(2): Show |
5 | HG00438.hp2 HG02683.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.665-2214_665-2193d others(24): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843347 | CTTTTTTT others(16): Show |
C | 1 | a0001c0011t0001g0098 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.665-2215_665-2193d others(25): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843347 | |||||||
chr16:87843407 | T | C | 134 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(131): Show |
135 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.665-2252A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843407 | |||||||
chr16:87843494 | C | T | 135 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(132): Show |
136 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.665-2339G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843494 | |||||||
chr16:87843591 | C | T | 1 | a0001c0001t0034g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.665-2436G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843591 | |||||||
chr16:87843613 | G | A | 3 | a0001c0001t0005g0092 a0001c0001t0005g0113 a0001c0001t0013g0160 |
3 | HG01361.hp1 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.665-2458C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843613 | |||||||
chr16:87843640 | T | C | 136 | a0001c0001t0001g0177 a0001c0001t0001g0202 a0001c0001t0001g0265 others(133): Show |
137 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.665-2485A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843640 | |||||||
chr16:87843695 | G | A | 1 | a0001c0011t0001g0098 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.665-2540C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843695 | |||||||
chr16:87843706 | G | A | 135 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(132): Show |
136 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.665-2551C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843706 | |||||||
chr16:87843707 | C | G | 135 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(132): Show |
136 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.665-2552G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843707 | |||||||
chr16:87843766 | G | A | 1 | a0001c0001t0025g0331 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.665-2611C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843766 | |||||||
chr16:87843962 | G | C | 2 | a0003c0014t0035g0008 a0003c0015t0042g0059 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.665-2807C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87843962 | |||||||
chr16:87844152 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.665-2997T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844152 | |||||||
chr16:87844155 | G | A | 1 | a0001c0001t0011g0372 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.665-3000C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844155 | |||||||
chr16:87844258 | G | A | 1 | a0001c0001t0002g0221 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.665-3103C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844258 | |||||||
chr16:87844289 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.665-3134C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844289 | |||||||
chr16:87844297 | C | T | 1 | a0001c0001t0034g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.665-3142G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844297 | |||||||
chr16:87844298 | G | A | 2 | a0001c0001t0007g0339 a0001c0001t0053g0081 |
2 | NA18983.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.665-3143C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844298 | |||||||
chr16:87844309 | C | G | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-3154G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844309 | |||||||
chr16:87844317 | C | T | 12 | a0001c0001t0006g0130 a0001c0001t0006g0165 a0001c0001t0017g0058 others(9): Show |
12 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.665-3162G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844317 | |||||||
chr16:87844323 | T | C | 14 | a0001c0001t0006g0130 a0001c0001t0006g0165 a0001c0001t0017g0058 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.665-3168A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844323 | |||||||
chr16:87844333 | G | A | 2 | a0001c0001t0005g0063 a0001c0002t0005g0012 |
2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.665-3178C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844333 | |||||||
chr16:87844346 | G | A | 14 | a0001c0001t0006g0130 a0001c0001t0006g0165 a0001c0001t0017g0058 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.665-3191C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844346 | |||||||
chr16:87844358 | C | T | 1 | a0001c0001t0024g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.665-3203G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844358 | |||||||
chr16:87844424 | C | T | 1 | a0004c0006t0014g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.665-3269G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844424 | |||||||
chr16:87844456 | G | A | 1 | a0001c0001t0003g0363 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-3301C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844456 | |||||||
chr16:87844466 | C | A | 141 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(138): Show |
142 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.665-3311G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844466 | |||||||
chr16:87844470 | G | A | 141 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(138): Show |
142 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.665-3315C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844470 | |||||||
chr16:87844527 | C | T | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665-3372G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844527 | |||||||
chr16:87844556 | T | G | 141 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(138): Show |
142 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.665-3401A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844556 | |||||||
chr16:87844559 | T | C | 141 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(138): Show |
142 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.665-3404A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844559 | |||||||
chr16:87844560 | G | T | 1 | a0001c0001t0003g0007 | 2 | HG03688.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.665-3405C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844560 | |||||||
chr16:87844613 | T | G | 38 | a0001c0001t0003g0007 a0001c0001t0003g0329 a0001c0001t0003g0332 others(35): Show |
39 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.665-3458A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844613 | |||||||
chr16:87844618 | G | A | 1 | a0001c0001t0005g0156 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.665-3463C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844618 | |||||||
chr16:87844662 | G | A | 37 | a0001c0001t0003g0007 a0001c0001t0003g0329 a0001c0001t0003g0332 others(34): Show |
38 | HG00438.hp1 HG00639.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.665-3507C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844662 | |||||||
chr16:87844662 | G | C | 1 | a0003c0014t0035g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.665-3507C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844662 | |||||||
chr16:87844760 | G | A | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-3605C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844760 | |||||||
chr16:87844767 | T | G | 1 | a0001c0002t0041g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.665-3612A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844767 | |||||||
chr16:87844788 | C | T | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-3633G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844788 | |||||||
chr16:87844793 | TCCAACCA others(8): Show |
T | 2 | a0001c0001t0004g0097 a0001c0001t0004g0189 |
2 | NA18954.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.665-3653_665-3639d others(17): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844793 | |||||||
chr16:87844870 | G | A | 140 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(137): Show |
141 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.665-3715C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844870 | |||||||
chr16:87844907 | G | A | 1 | a0001c0002t0008g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.665-3752C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844907 | |||||||
chr16:87844964 | G | A | 127 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(124): Show |
128 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.665-3809C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87844964 | |||||||
chr16:87845045 | C | A | 127 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(124): Show |
128 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.665-3890G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845045 | |||||||
chr16:87845081 | G | C | 2 | a0001c0001t0029g0162 a0001c0001t0029g0163 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.665-3926C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845081 | |||||||
chr16:87845102 | A | G | 318 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(315): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.665-3947T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845102 | |||||||
chr16:87845177 | C | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(152): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.665-4022G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845177 | |||||||
chr16:87845181 | G | A | 1 | a0001c0001t0002g0276 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.665-4026C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845181 | |||||||
chr16:87845193 | C | CT | 141 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(138): Show |
142 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.665-4039_665-4038i others(3): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845193 | |||||||
chr16:87845216 | G | A | 141 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(138): Show |
142 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.665-4061C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845216 | |||||||
chr16:87845235 | G | A | 1 | a0001c0001t0069g0321 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.665-4080C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845235 | |||||||
chr16:87845277 | C | G | 140 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(137): Show |
141 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.665-4122G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845277 | |||||||
chr16:87845343 | C | T | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-4188G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845343 | |||||||
chr16:87845356 | G | T | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665-4201C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845356 | |||||||
chr16:87845358 | A | G | 321 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(318): Show |
327 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.665-4203T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845358 | |||||||
chr16:87845362 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0059g0212 |
2 | NA18986.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.665-4207C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845362 | |||||||
chr16:87845404 | G | C | 2 | a0001c0002t0027g0018 a0001c0002t0027g0019 |
2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.665-4249C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845404 | |||||||
chr16:87845411 | T | TGCCCACC others(13): Show |
1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-4276_665-4257d others(22): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845411 | |||||||
chr16:87845472 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.665-4317C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845472 | |||||||
chr16:87845478 | C | G | 1 | a0001c0001t0046g0109 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.665-4323G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845478 | |||||||
chr16:87845491 | C | T | 1 | a0001c0001t0006g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.665-4336G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845491 | |||||||
chr16:87845509 | T | TGCCCACC others(53): Show |
1 | a0001c0001t0003g0359 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.665-4355_665-4354i others(62): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845509 | |||||||
chr16:87845510 | G | A | 1 | a0001c0002t0001g0016 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.665-4355C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845510 | |||||||
chr16:87845516 | T | C | 1 | a0001c0001t0003g0359 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.665-4361A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845516 | |||||||
chr16:87845516 | T | TCCAGGCA others(135): Show |
1 | a0001c0001t0034g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.665-4362_665-4361i others(144): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845516 | |||||||
chr16:87845516 | T | TCCAGGCA others(75): Show |
138 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(135): Show |
139 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.665-4362_665-4361i others(84): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845516 | |||||||
chr16:87845531 | C | T | 1 | a0001c0001t0003g0363 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-4376G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845531 | |||||||
chr16:87845543 | G | A | 1 | a0001c0001t0003g0363 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-4388C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845543 | |||||||
chr16:87845552 | G | A | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-4397C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845552 | |||||||
chr16:87845557 | C | CCCCAGAG others(76): Show |
1 | a0001c0001t0003g0363 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-4403_665-4402i others(85): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845557 | |||||||
chr16:87845557 | C | T | 139 | a0001c0001t0001g0177 a0001c0001t0001g0265 a0001c0001t0001g0268 others(136): Show |
140 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.665-4402G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845557 | |||||||
chr16:87845643 | T | A | 1 | a0001c0001t0003g0363 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.665-4488A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845643 | |||||||
chr16:87845695 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.665-4540C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845695 | |||||||
chr16:87845753 | C | G | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-4598G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845753 | |||||||
chr16:87845786 | G | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(170): Show |
178 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.665-4631C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845786 | |||||||
chr16:87845798 | T | G | 1 | a0001c0002t0001g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.665-4643A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845798 | |||||||
chr16:87845823 | G | C | 1 | a0001c0001t0004g0189 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.665-4668C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845823 | |||||||
chr16:87845849 | G | A | 1 | a0003c0008t0064g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.665-4694C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845849 | |||||||
chr16:87845880 | G | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(170): Show |
178 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.665-4725C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845880 | |||||||
chr16:87845916 | G | T | 179 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(176): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.665-4761C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845916 | |||||||
chr16:87845927 | C | T | 6 | a0001c0001t0014g0055 a0001c0001t0014g0247 a0001c0001t0014g0248 others(3): Show |
6 | HG02622.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.665-4772G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845927 | |||||||
chr16:87845956 | C | A | 179 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(176): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.665-4801G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845956 | |||||||
chr16:87845970 | G | A | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665-4815C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87845970 | |||||||
chr16:87846060 | T | G | 23 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(20): Show |
24 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.665-4905A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846060 | |||||||
chr16:87846119 | C | T | 2 | a0001c0001t0065g0371 a0003c0015t0042g0059 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.665-4964G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846119 | |||||||
chr16:87846138 | GGCCCAGG others(14): Show |
G | 1 | a0001c0001t0004g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.665-5004_665-4984d others(23): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846138 | |||||||
chr16:87846163 | A | G | 25 | a0001c0001t0006g0069 a0001c0001t0006g0130 a0001c0001t0006g0131 others(22): Show |
26 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.665-5008T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846163 | |||||||
chr16:87846210 | G | C | 1 | a0003c0008t0064g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.665-5055C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846210 | |||||||
chr16:87846233 | A | C | 23 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(20): Show |
24 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.665-5078T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846233 | |||||||
chr16:87846259 | T | C | 23 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(20): Show |
24 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.665-5104A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846259 | |||||||
chr16:87846362 | C | A | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665-5207G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846362 | |||||||
chr16:87846405 | G | A | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.665-5250C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846405 | |||||||
chr16:87846454 | C | T | 5 | a0002c0004t0019g0013 a0002c0004t0019g0046 a0002c0004t0043g0047 others(2): Show |
5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+5270G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846454 | |||||||
chr16:87846483 | G | A | 15 | a0001c0001t0006g0131 a0001c0001t0006g0132 a0001c0001t0014g0055 others(12): Show |
15 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.664+5241C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846483 | |||||||
chr16:87846609 | A | G | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+5115T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846609 | |||||||
chr16:87846624 | G | T | 1 | a0001c0002t0008g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.664+5100C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846624 | |||||||
chr16:87846660 | C | G | 1 | a0001c0001t0014g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.664+5064G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846660 | |||||||
chr16:87846779 | C | T | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+4945G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846779 | |||||||
chr16:87846797 | C | T | 1 | a0001c0001t0005g0113 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.664+4927G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846797 | |||||||
chr16:87846814 | A | G | 23 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(20): Show |
24 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.664+4910T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846814 | |||||||
chr16:87846855 | G | A | 1 | a0001c0001t0070g0366 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.664+4869C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846855 | |||||||
chr16:87846879 | C | T | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.664+4845G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846879 | |||||||
chr16:87846964 | C | T | 1 | a0001c0002t0005g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.664+4760G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846964 | |||||||
chr16:87846975 | G | C | 1 | a0001c0001t0003g0375 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.664+4749C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87846975 | |||||||
chr16:87847063 | C | T | 40 | a0001c0001t0002g0077 a0001c0001t0002g0121 a0001c0001t0002g0122 others(37): Show |
40 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.664+4661G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847063 | |||||||
chr16:87847096 | C | T | 11 | a0001c0001t0006g0165 a0001c0001t0017g0058 a0001c0001t0017g0094 others(8): Show |
11 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.664+4628G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847096 | |||||||
chr16:87847097 | G | A | 1 | a0003c0014t0035g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.664+4627C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847097 | |||||||
chr16:87847186 | C | T | 11 | a0001c0001t0006g0165 a0001c0001t0017g0058 a0001c0001t0017g0094 others(8): Show |
11 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.664+4538G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847186 | |||||||
chr16:87847286 | T | C | 5 | a0002c0004t0019g0013 a0002c0004t0019g0046 a0002c0004t0043g0047 others(2): Show |
5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+4438A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847286 | |||||||
chr16:87847307 | G | A | 1 | a0001c0001t0013g0218 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.664+4417C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847307 | |||||||
chr16:87847325 | G | A | 1 | a0001c0002t0066g0319 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.664+4399C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847325 | |||||||
chr16:87847340 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.664+4384C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847340 | |||||||
chr16:87847361 | A | G | 183 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(180): Show |
188 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.664+4363T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847361 | |||||||
chr16:87847368 | G | C | 1 | a0001c0002t0041g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.664+4356C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847368 | |||||||
chr16:87847387 | AGCCAGAT others(4): Show |
A | 6 | a0001c0001t0001g0099 a0001c0001t0001g0188 a0001c0001t0001g0191 others(3): Show |
6 | HG00673.hp1 HG02027.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.664+4326_664+4336d others(13): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847387 | |||||||
chr16:87847414 | C | T | 10 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0006g0130 others(7): Show |
10 | HG00733.hp2 HG02965.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.664+4310G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847414 | |||||||
chr16:87847523 | C | T | 1 | a0001c0002t0020g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.664+4201G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847523 | |||||||
chr16:87847587 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG00140.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.664+4137C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847587 | |||||||
chr16:87847608 | G | C | 5 | a0002c0004t0019g0013 a0002c0004t0019g0046 a0002c0004t0043g0047 others(2): Show |
5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+4116C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847608 | |||||||
chr16:87847682 | C | G | 1 | a0001c0002t0001g0016 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.664+4042G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847682 | |||||||
chr16:87847683 | C | T | 2 | a0001c0002t0006g0048 a0001c0002t0039g0050 |
2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.664+4041G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847683 | |||||||
chr16:87847684 | A | G | 23 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(20): Show |
24 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.664+4040T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847684 | |||||||
chr16:87847689 | C | T | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+4035G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847689 | |||||||
chr16:87847709 | A | G | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+4015T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847709 | |||||||
chr16:87847759 | G | C | 4 | a0001c0001t0006g0165 a0001c0001t0026g0127 a0001c0001t0040g0164 others(1): Show |
4 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+3965C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847759 | |||||||
chr16:87847777 | C | T | 26 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(23): Show |
27 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.664+3947G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847777 | |||||||
chr16:87847828 | A | G | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+3896T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847828 | |||||||
chr16:87847850 | A | G | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664+3874T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847850 | |||||||
chr16:87847868 | G | A | 4 | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0023 others(1): Show |
4 | HG00099.hp1 HG00323.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+3856C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847868 | |||||||
chr16:87847961 | C | A | 1 | a0003c0014t0035g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.664+3763G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847961 | |||||||
chr16:87847979 | G | A | 2 | a0001c0001t0007g0339 a0001c0001t0053g0081 |
2 | NA18983.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.664+3745C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87847979 | |||||||
chr16:87848021 | G | A | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+3703C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848021 | |||||||
chr16:87848124 | G | C | 13 | a0001c0001t0008g0145 a0001c0001t0008g0146 a0001c0001t0008g0147 others(10): Show |
13 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.664+3600C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848124 | |||||||
chr16:87848139 | T | TC | 157 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0002g0077 others(154): Show |
159 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.664+3584_664+3585i others(3): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848139 | |||||||
chr16:87848238 | A | G | 2 | a0001c0001t0067g0323 a0003c0014t0035g0008 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.664+3486T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848238 | |||||||
chr16:87848282 | C | T | 1 | a0001c0001t0011g0365 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.664+3442G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848282 | |||||||
chr16:87848438 | C | A | 2 | a0001c0001t0003g0368 a0001c0001t0003g0369 |
2 | HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.664+3286G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848438 | |||||||
chr16:87848480 | G | A | 1 | a0001c0001t0005g0167 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.664+3244C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848480 | |||||||
chr16:87848518 | T | C | 173 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0002g0077 others(170): Show |
175 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.664+3206A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848518 | |||||||
chr16:87848528 | T | C | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.664+3196A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848528 | |||||||
chr16:87848562 | G | C | 2 | a0001c0002t0020g0031 a0001c0002t0020g0032 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.664+3162C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848562 | |||||||
chr16:87848603 | A | G | 172 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0002g0077 others(169): Show |
174 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.664+3121T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848603 | |||||||
chr16:87848691 | A | G | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+3033T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848691 | |||||||
chr16:87848729 | C | T | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+2995G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848729 | |||||||
chr16:87848773 | C | G | 1 | a0001c0001t0030g0311 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.664+2951G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848773 | |||||||
chr16:87848824 | C | T | 22 | a0001c0001t0002g0070 a0001c0001t0006g0069 a0001c0001t0006g0131 others(19): Show |
23 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.664+2900G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848824 | |||||||
chr16:87848827 | C | G | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0273 others(2): Show |
5 | HG00140.hp2 HG00738.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+2897G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848827 | |||||||
chr16:87848829 | T | C | 3 | a0001c0001t0002g0086 a0001c0001t0002g0206 a0001c0001t0009g0082 |
3 | HG00544.hp2 NA18988.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.664+2895A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848829 | |||||||
chr16:87848835 | C | T | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+2889G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848835 | |||||||
chr16:87848876 | G | T | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664+2848C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848876 | |||||||
chr16:87848890 | CA | C | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+2833delT | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848890 | |||||||
chr16:87848903 | C | T | 167 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0002g0077 others(164): Show |
169 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.664+2821G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848903 | |||||||
chr16:87848915 | A | AGGCAAGA others(8): Show |
167 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0002g0077 others(164): Show |
169 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.664+2808_664+2809i others(17): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848915 | |||||||
chr16:87848933 | A | G | 167 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0002g0077 others(164): Show |
169 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.664+2791T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848933 | |||||||
chr16:87848964 | C | G | 1 | a0003c0008t0064g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.664+2760G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87848964 | |||||||
chr16:87849037 | C | A | 1 | a0001c0001t0068g0376 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.664+2687G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849037 | |||||||
chr16:87849089 | C | A | 152 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0002g0077 others(149): Show |
153 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.664+2635G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849089 | |||||||
chr16:87849223 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.664+2501G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849223 | |||||||
chr16:87849230 | TG | T | 165 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0002g0077 others(162): Show |
167 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.664+2493delC | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849230 | |||||||
chr16:87849234 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.664+2490C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849234 | |||||||
chr16:87849451 | T | C | 19 | a0001c0001t0001g0056 a0001c0001t0001g0151 a0001c0001t0001g0153 others(16): Show |
19 | HG00438.hp2 HG00597.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.664+2273A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849451 | |||||||
chr16:87849483 | C | T | 105 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0001c0001t0002g0077 others(102): Show |
106 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.664+2241G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849483 | |||||||
chr16:87849536 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.664+2188G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849536 | |||||||
chr16:87849553 | G | A | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+2171C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849553 | |||||||
chr16:87849592 | C | T | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.664+2132G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849592 | |||||||
chr16:87849638 | A | G | 1 | a0001c0002t0041g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.664+2086T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849638 | |||||||
chr16:87849645 | C | T | 5 | a0001c0001t0065g0371 a0001c0002t0001g0037 a0001c0002t0041g0038 others(2): Show |
5 | HG02451.hp1 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+2079G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849645 | |||||||
chr16:87849657 | A | G | 5 | a0001c0001t0003g0362 a0001c0001t0003g0363 a0001c0001t0003g0364 others(2): Show |
5 | NA18939.hp2 NA18963.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+2067T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849657 | |||||||
chr16:87849712 | G | C | 1 | a0001c0001t0060g0144 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.664+2012C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849712 | |||||||
chr16:87849853 | A | T | 1 | a0001c0001t0030g0311 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.664+1871T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849853 | |||||||
chr16:87849861 | G | A | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.664+1863C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87849861 | |||||||
chr16:87850115 | A | C | 330 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(327): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.664+1609T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850115 | |||||||
chr16:87850127 | G | A | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664+1597C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850127 | |||||||
chr16:87850129 | C | T | 1 | a0001c0001t0013g0281 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.664+1595G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850129 | |||||||
chr16:87850130 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.664+1594C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850130 | |||||||
chr16:87850139 | C | G | 1 | a0001c0001t0054g0120 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.664+1585G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850139 | |||||||
chr16:87850213 | G | T | 2 | a0001c0001t0065g0371 a0003c0015t0042g0059 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.664+1511C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850213 | |||||||
chr16:87850236 | C | T | 1 | a0001c0001t0071g0338 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.664+1488G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850236 | |||||||
chr16:87850312 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0151 |
2 | NA18960.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.664+1412C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850312 | |||||||
chr16:87850335 | C | T | 1 | a0001c0002t0045g0035 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.664+1389G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850335 | |||||||
chr16:87850383 | T | C | 2 | a0001c0001t0067g0323 a0003c0014t0035g0008 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.664+1341A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850383 | |||||||
chr16:87850391 | G | A | 2 | a0001c0001t0004g0074 a0001c0001t0011g0330 |
2 | HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.664+1333C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850391 | |||||||
chr16:87850502 | G | A | 1 | a0001c0001t0015g0152 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.664+1222C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850502 | |||||||
chr16:87850503 | A | G | 1 | a0001c0001t0015g0152 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.664+1221T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850503 | |||||||
chr16:87850729 | A | T | 1 | a0001c0001t0015g0152 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.664+995T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850729 | |||||||
chr16:87850734 | T | C | 3 | a0001c0001t0065g0371 a0001c0002t0041g0038 a0003c0015t0042g0059 |
3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.664+990A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850734 | |||||||
chr16:87850735 | G | A | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.664+989C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850735 | |||||||
chr16:87850758 | T | C | 3 | a0001c0001t0065g0371 a0001c0002t0041g0038 a0003c0015t0042g0059 |
3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.664+966A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850758 | |||||||
chr16:87850765 | G | A | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.664+959C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850765 | |||||||
chr16:87850839 | A | G | 1 | a0001c0002t0001g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.664+885T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850839 | |||||||
chr16:87850873 | G | C | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.664+851C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850873 | |||||||
chr16:87850941 | A | G | 151 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0177 others(148): Show |
152 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.664+783T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87850941 | |||||||
chr16:87851092 | A | G | 1 | a0001c0001t0024g0355 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.664+632T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851092 | |||||||
chr16:87851156 | G | GTCTGAGT others(27): Show |
6 | a0001c0001t0015g0065 a0001c0001t0015g0066 a0001c0001t0015g0067 others(3): Show |
6 | NA18948.hp1 NA18964.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.664+534_664+567dup others(34): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851156 | |||||||
chr16:87851192 | C | T | 3 | a0001c0001t0065g0371 a0001c0002t0041g0038 a0003c0015t0042g0059 |
3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.664+532G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851192 | |||||||
chr16:87851289 | G | A | 1 | a0001c0001t0006g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.664+435C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851289 | |||||||
chr16:87851295 | C | T | 2 | a0001c0001t0020g0226 a0001c0002t0020g0032 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.664+429G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851295 | |||||||
chr16:87851308 | G | A | 3 | a0001c0001t0065g0371 a0001c0002t0041g0038 a0003c0015t0042g0059 |
3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.664+416C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851308 | |||||||
chr16:87851359 | T | G | 3 | a0001c0001t0065g0371 a0001c0002t0041g0038 a0003c0015t0042g0059 |
3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.664+365A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851359 | |||||||
chr16:87851446 | G | A | 2 | a0001c0001t0020g0226 a0001c0002t0020g0032 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.664+278C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851446 | |||||||
chr16:87851663 | G | A | 1 | a0001c0001t0068g0376 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.664+61C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851663 | |||||||
chr16:87851696 | G | A | 5 | a0001c0001t0002g0259 a0001c0001t0002g0260 a0001c0001t0002g0261 others(2): Show |
5 | HG00738.hp1 HG01978.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+28C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 2/9 | chr16 | 87851696 | |||||||
chr16:87851867 | A | G | 3 | a0001c0001t0065g0371 a0001c0002t0041g0038 a0003c0015t0042g0059 |
3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.539-18T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87851867 | |||||||
chr16:87851936 | C | A | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539-87G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87851936 | |||||||
chr16:87851999 | T | C | 2 | a0001c0001t0006g0130 a0003c0008t0064g0318 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.539-150A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87851999 | |||||||
chr16:87852006 | C | G | 4 | a0001c0001t0065g0371 a0001c0002t0001g0037 a0001c0002t0041g0038 others(1): Show |
4 | HG02451.hp1 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.539-157G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852006 | |||||||
chr16:87852007 | G | A | 1 | a0001c0001t0067g0323 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.539-158C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852007 | |||||||
chr16:87852110 | C | G | 1 | a0001c0001t0002g0149 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.539-261G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852110 | |||||||
chr16:87852129 | T | C | 7 | a0001c0001t0065g0371 a0001c0001t0067g0323 a0001c0002t0001g0037 others(4): Show |
7 | HG02451.hp1 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.539-280A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852129 | |||||||
chr16:87852163 | G | A | 1 | a0001c0001t0009g0107 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.539-314C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852163 | |||||||
chr16:87852357 | C | T | 5 | a0002c0004t0019g0013 a0002c0004t0019g0046 a0002c0004t0043g0047 others(2): Show |
5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-508G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852357 | |||||||
chr16:87852365 | C | T | 1 | a0001c0001t0014g0250 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.539-516G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852365 | |||||||
chr16:87852366 | G | A | 3 | a0001c0001t0002g0091 a0001c0001t0067g0323 a0003c0014t0035g0008 |
3 | HG02965.hp1 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.539-517C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852366 | |||||||
chr16:87852393 | C | T | 5 | a0002c0004t0019g0013 a0002c0004t0019g0046 a0002c0004t0043g0047 others(2): Show |
5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-544G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852393 | |||||||
chr16:87852423 | T | C | 1 | a0003c0008t0064g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.539-574A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852423 | |||||||
chr16:87852427 | G | A | 12 | a0001c0001t0006g0069 a0001c0001t0014g0055 a0001c0001t0014g0247 others(9): Show |
13 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.539-578C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852427 | |||||||
chr16:87852429 | G | A | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-580C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852429 | |||||||
chr16:87852435 | C | A | 1 | a0001c0002t0016g0034 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.539-586G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852435 | |||||||
chr16:87852531 | A | G | 3 | a0001c0001t0065g0371 a0001c0002t0041g0038 a0003c0015t0042g0059 |
3 | HG02451.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.539-682T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852531 | |||||||
chr16:87852557 | T | C | 176 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0177 others(173): Show |
178 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.539-708A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852557 | |||||||
chr16:87852636 | C | CCTCTGTC others(9): Show |
1 | a0001c0001t0004g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-788_539-787ins others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852636 | |||||||
chr16:87852636 | CTCTGTGT others(5): Show |
C | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539-799_539-788del others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852636 | |||||||
chr16:87852638 | C | CTG | 28 | a0001c0001t0001g0093 a0001c0001t0001g0104 a0001c0001t0001g0142 others(25): Show |
28 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.539-791_539-790dup others(2): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | C | CTGTG | 22 | a0001c0001t0001g0202 a0001c0001t0001g0231 a0001c0001t0001g0257 others(19): Show |
22 | HG00544.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.539-793_539-790dup others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | C | CTGTGTG | 26 | a0001c0001t0001g0154 a0001c0001t0001g0213 a0001c0001t0001g0230 others(23): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.539-795_539-790dup others(6): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | C | CTGTGTGT others(1): Show |
19 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0068 others(16): Show |
21 | HG00423.hp1 HG00621.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.539-797_539-790dup others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | C | CTGTGTGT others(3): Show |
32 | a0001c0001t0001g0056 a0001c0001t0001g0143 a0001c0001t0001g0148 others(29): Show |
32 | HG00140.hp1 HG00438.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.539-799_539-790dup others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | C | CTGTGTGT others(5): Show |
41 | a0001c0001t0001g0075 a0001c0001t0001g0100 a0001c0001t0001g0102 others(38): Show |
41 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.539-801_539-790dup others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | C | CTGTGTGT others(7): Show |
24 | a0001c0001t0001g0099 a0001c0001t0001g0116 a0001c0001t0001g0126 others(21): Show |
24 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.539-803_539-790dup others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | C | CTGTGTGT others(9): Show |
1 | a0001c0001t0028g0244 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.539-805_539-790dup others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | C | CTGTGTGT others(11): Show |
2 | a0001c0001t0001g0106 a0001c0001t0001g0139 |
2 | NA19085.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.539-807_539-790dup others(18): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | C | G | 2 | a0001c0001t0004g0076 a0003c0015t0042g0059 |
2 | HG02451.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.539-789G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | CTG | C | 31 | a0001c0001t0001g0108 a0001c0001t0001g0274 a0001c0001t0002g0003 others(28): Show |
33 | HG00140.hp2 HG00558.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.539-791_539-790del others(2): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | CTGTG | C | 29 | a0001c0001t0001g0268 a0001c0001t0002g0183 a0001c0001t0002g0272 others(26): Show |
29 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.539-793_539-790del others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | CTGTGTG | C | 45 | a0001c0001t0001g0078 a0001c0001t0001g0177 a0001c0001t0001g0265 others(42): Show |
46 | HG00438.hp1 HG00733.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.539-795_539-790del others(6): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | CTGTGTGT others(1): Show |
C | 4 | a0001c0001t0005g0063 a0001c0001t0017g0058 a0001c0001t0017g0094 others(1): Show |
4 | HG02258.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.539-797_539-790del others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | CTGTGTGT others(3): Show |
C | 6 | a0001c0001t0006g0165 a0001c0001t0017g0117 a0001c0001t0017g0217 others(3): Show |
6 | HG01081.hp2 HG01167.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.539-799_539-790del others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0005g0167 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.539-801_539-790del others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0002g0280 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.539-803_539-790del others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852638 | CTGTGTGT others(15): Show |
C | 1 | a0001c0002t0055g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.539-811_539-790del others(22): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852638 | |||||||
chr16:87852641 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0011g0374 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.539-793_539-792ins others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852641 | |||||||
chr16:87852643 | T | TGTGTGTG others(5): Show |
3 | a0001c0001t0030g0310 a0001c0001t0030g0311 a0001c0002t0001g0001 |
5 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-795_539-794ins others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852643 | |||||||
chr16:87852657 | T | C | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-808A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852657 | |||||||
chr16:87852665 | T | A | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-816A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852665 | |||||||
chr16:87852669 | TGTGTGTG others(8): Show |
T | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-835_539-821del others(15): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852669 | |||||||
chr16:87852686 | G | T | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-837C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852686 | |||||||
chr16:87852687 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0299 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.539-839_539-838ins others(11): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852687 | |||||||
chr16:87852687 | T | TGTGTGTG others(6): Show |
1 | a0001c0001t0001g0237 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.539-839_539-838ins others(13): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852687 | |||||||
chr16:87852688 | T | G | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-839A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852688 | |||||||
chr16:87852689 | G | T | 1 | a0001c0001t0001g0299 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.539-840C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852689 | |||||||
chr16:87852708 | A | G | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-859T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852708 | |||||||
chr16:87852736 | T | C | 5 | a0002c0004t0019g0013 a0002c0004t0019g0046 a0002c0004t0043g0047 others(2): Show |
5 | HG02630.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-887A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852736 | |||||||
chr16:87852742 | T | C | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-893A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852742 | |||||||
chr16:87852770 | C | T | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-921G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852770 | |||||||
chr16:87852772 | A | T | 1 | a0001c0001t0072g0381 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.539-923T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852772 | |||||||
chr16:87852778 | G | A | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-929C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852778 | |||||||
chr16:87852779 | C | G | 176 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0177 others(173): Show |
178 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.539-930G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852779 | |||||||
chr16:87852780 | G | A | 1 | a0001c0001t0033g0377 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.539-931C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852780 | |||||||
chr16:87852830 | C | T | 1 | a0001c0002t0001g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.539-981G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852830 | |||||||
chr16:87852833 | C | T | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539-984G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852833 | |||||||
chr16:87852884 | C | T | 142 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(139): Show |
146 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.539-1035G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852884 | |||||||
chr16:87852933 | G | C | 3 | a0001c0001t0020g0226 a0001c0002t0020g0031 a0001c0002t0020g0032 |
3 | HG02258.hp2 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.539-1084C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852933 | |||||||
chr16:87852934 | G | A | 18 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0086 others(15): Show |
20 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.539-1085C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852934 | |||||||
chr16:87852939 | C | T | 170 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(167): Show |
175 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.539-1090G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852939 | |||||||
chr16:87852944 | G | A | 4 | a0001c0001t0006g0269 a0001c0001t0022g0169 a0001c0001t0022g0192 others(1): Show |
4 | HG00735.hp2 HG01433.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-1095C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852944 | |||||||
chr16:87852947 | G | A | 1 | a0001c0001t0006g0269 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.539-1098C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87852947 | |||||||
chr16:87853020 | A | G | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.539-1171T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853020 | |||||||
chr16:87853040 | C | G | 1 | a0001c0001t0006g0269 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.539-1191G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853040 | |||||||
chr16:87853043 | T | C | 1 | a0001c0001t0004g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-1194A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853043 | |||||||
chr16:87853044 | C | T | 1 | a0001c0001t0004g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-1195G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853044 | |||||||
chr16:87853053 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.539-1204C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853053 | |||||||
chr16:87853094 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.539-1245G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853094 | |||||||
chr16:87853095 | G | A | 1 | a0001c0002t0045g0035 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.539-1246C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853095 | |||||||
chr16:87853105 | CTT | C | 21 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.539-1258_539-1257d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853105 | |||||||
chr16:87853120 | T | A | 144 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(141): Show |
148 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.539-1271A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853120 | |||||||
chr16:87853123 | G | T | 1 | a0003c0014t0035g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.539-1274C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853123 | |||||||
chr16:87853130 | C | T | 2 | a0001c0001t0009g0181 a0001c0001t0009g0291 |
2 | NA18980.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.539-1281G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853130 | |||||||
chr16:87853132 | C | T | 1 | a0001c0001t0004g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-1283G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853132 | |||||||
chr16:87853228 | C | T | 22 | a0001c0001t0006g0069 a0001c0001t0006g0131 a0001c0001t0006g0132 others(19): Show |
23 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.539-1379G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853228 | |||||||
chr16:87853266 | G | A | 1 | a0001c0001t0003g0332 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.539-1417C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853266 | |||||||
chr16:87853296 | C | T | 1 | a0001c0001t0005g0167 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.539-1447G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853296 | |||||||
chr16:87853300 | T | C | 1 | a0001c0002t0010g0014 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.539-1451A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853300 | |||||||
chr16:87853328 | G | A | 3 | a0001c0002t0026g0017 a0001c0002t0027g0018 a0001c0002t0027g0019 |
3 | HG02145.hp1 HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.539-1479C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853328 | |||||||
chr16:87853443 | A | G | 11 | a0001c0001t0002g0005 a0001c0001t0002g0086 a0001c0001t0002g0088 others(8): Show |
12 | HG00544.hp2 HG02129.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.539-1594T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853443 | |||||||
chr16:87853498 | C | G | 1 | a0001c0001t0017g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539-1649G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853498 | |||||||
chr16:87853595 | T | C | 131 | a0001c0001t0001g0078 a0001c0001t0001g0085 a0001c0001t0001g0177 others(128): Show |
132 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.539-1746A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853595 | |||||||
chr16:87853601 | G | A | 1 | a0001c0002t0041g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.539-1752C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853601 | |||||||
chr16:87853656 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.539-1807C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853656 | |||||||
chr16:87853701 | G | A | 5 | a0001c0001t0001g0075 a0001c0001t0001g0142 a0001c0001t0004g0074 others(2): Show |
5 | HG01978.hp1 HG02293.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-1852C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853701 | |||||||
chr16:87853712 | A | AGCTTTCT others(1): Show |
17 | a0001c0001t0001g0056 a0001c0001t0001g0151 a0001c0001t0001g0153 others(14): Show |
17 | HG00438.hp2 HG00597.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.539-1871_539-1864d others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853712 | |||||||
chr16:87853713 | G | T | 1 | a0001c0001t0004g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-1864C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853713 | |||||||
chr16:87853734 | C | T | 1 | a0003c0008t0064g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.539-1885G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853734 | |||||||
chr16:87853735 | C | T | 1 | a0001c0001t0054g0120 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.539-1886G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853735 | |||||||
chr16:87853752 | C | T | 1 | a0001c0001t0012g0129 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.539-1903G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853752 | |||||||
chr16:87853781 | A | G | 5 | a0001c0001t0013g0218 a0001c0001t0018g0312 a0001c0001t0018g0313 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-1932T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853781 | |||||||
chr16:87853805 | G | A | 1 | a0001c0001t0017g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539-1956C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853805 | |||||||
chr16:87853825 | G | C | 2 | a0001c0002t0006g0002 a0001c0002t0010g0049 |
3 | HG02486.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.539-1976C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853825 | |||||||
chr16:87853836 | A | C | 1 | a0001c0001t0011g0324 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.539-1987T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853836 | |||||||
chr16:87853837 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.539-1988G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853837 | |||||||
chr16:87853845 | C | A | 11 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0240 others(8): Show |
11 | HG01123.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.539-1996G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853845 | |||||||
chr16:87853877 | G | C | 329 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(326): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.539-2028C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853877 | |||||||
chr16:87853885 | T | C | 1 | a0001c0001t0067g0323 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.539-2036A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853885 | |||||||
chr16:87853890 | A | G | 16 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0273 others(13): Show |
16 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.539-2041T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853890 | |||||||
chr16:87853898 | CGCGGCTG others(8): Show |
C | 39 | a0001c0001t0001g0075 a0001c0001t0001g0100 a0001c0001t0001g0168 others(36): Show |
39 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.539-2064_539-2050d others(17): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853898 | |||||||
chr16:87853915 | C | T | 3 | a0001c0002t0008g0044 a0002c0004t0019g0046 a0002c0004t0044g0045 |
3 | HG02630.hp2 HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.539-2066G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853915 | |||||||
chr16:87853924 | C | T | 1 | a0001c0002t0002g0015 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.539-2075G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853924 | |||||||
chr16:87853936 | G | A | 5 | a0001c0001t0002g0005 a0001c0001t0002g0088 a0001c0001t0002g0183 others(2): Show |
6 | HG02129.hp2 NA18947.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.539-2087C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853936 | |||||||
chr16:87853939 | TG | T | 19 | a0001c0001t0002g0298 a0001c0001t0006g0130 a0001c0001t0006g0165 others(16): Show |
19 | HG01167.hp2 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.539-2091delC | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853939 | |||||||
chr16:87853954 | G | A | 77 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0203 others(74): Show |
79 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.539-2105C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853954 | |||||||
chr16:87853960 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.539-2111G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853960 | |||||||
chr16:87853994 | C | T | 1 | a0001c0001t0006g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.539-2145G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87853994 | |||||||
chr16:87854072 | G | C | 10 | a0001c0001t0001g0139 a0001c0001t0001g0268 a0001c0001t0002g0091 others(7): Show |
10 | HG00642.hp2 HG01109.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.539-2223C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | |||||||
chr16:87854072 | G | GC | 121 | a0001c0001t0001g0071 a0001c0001t0001g0093 a0001c0001t0001g0106 others(118): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.539-2224dupG | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | |||||||
chr16:87854072 | G | GCC | 56 | a0001c0001t0001g0104 a0001c0001t0001g0128 a0001c0001t0001g0154 others(53): Show |
56 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.539-2225_539-2224d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | |||||||
chr16:87854072 | G | GCCC | 23 | a0001c0001t0001g0072 a0001c0001t0002g0122 a0001c0001t0002g0261 others(20): Show |
23 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.539-2226_539-2224d others(5): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | |||||||
chr16:87854072 | G | GCCCC | 30 | a0001c0001t0001g0213 a0001c0001t0001g0265 a0001c0001t0002g0121 others(27): Show |
31 | HG00280.hp2 HG00597.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.539-2227_539-2224d others(6): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | |||||||
chr16:87854072 | GC | G | 41 | a0001c0001t0001g0075 a0001c0001t0001g0102 a0001c0001t0001g0168 others(38): Show |
41 | HG00642.hp1 HG01081.hp2 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.539-2224delG | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | |||||||
chr16:87854072 | GCC | G | 58 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0078 others(55): Show |
59 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.539-2225_539-2224d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854072 | |||||||
chr16:87854074 | C | G | 1 | a0008c0010t0001g0210 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.539-2225G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854074 | |||||||
chr16:87854108 | C | A | 1 | a0001c0001t0067g0323 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.539-2259G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854108 | |||||||
chr16:87854111 | T | A | 50 | a0001c0001t0001g0085 a0001c0001t0001g0093 a0001c0001t0001g0274 others(47): Show |
52 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.539-2262A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854111 | |||||||
chr16:87854114 | C | T | 25 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0116 others(22): Show |
25 | HG00558.hp2 HG00673.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.539-2265G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854114 | |||||||
chr16:87854142 | G | T | 200 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0071 others(197): Show |
206 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.539-2293C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854142 | |||||||
chr16:87854145 | T | C | 203 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0071 others(200): Show |
209 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.539-2296A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854145 | |||||||
chr16:87854158 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.539-2309C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854158 | |||||||
chr16:87854194 | A | G | 3 | a0001c0001t0001g0187 a0001c0001t0002g0003 a0001c0001t0004g0079 |
4 | HG02056.hp2 NA18940.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-2345T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854194 | |||||||
chr16:87854200 | G | A | 72 | a0001c0001t0001g0085 a0001c0001t0001g0093 a0001c0001t0001g0116 others(69): Show |
73 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.539-2351C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854200 | |||||||
chr16:87854281 | T | C | 1 | a0001c0001t0062g0352 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.539-2432A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854281 | |||||||
chr16:87854350 | A | G | 2 | a0001c0002t0010g0014 a0002c0004t0019g0013 |
2 | HG00639.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.539-2501T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854350 | |||||||
chr16:87854352 | G | C | 1 | a0001c0001t0013g0277 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.539-2503C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854352 | |||||||
chr16:87854438 | A | G | 29 | a0001c0001t0004g0282 a0001c0001t0006g0165 a0001c0001t0010g0266 others(26): Show |
29 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.539-2589T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854438 | |||||||
chr16:87854462 | G | A | 4 | a0001c0002t0008g0044 a0002c0004t0019g0046 a0002c0004t0043g0047 others(1): Show |
4 | HG02630.hp2 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-2613C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854462 | |||||||
chr16:87854482 | C | A | 59 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0177 others(56): Show |
61 | HG00323.hp2 HG00642.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.539-2633G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854482 | |||||||
chr16:87854513 | T | C | 271 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(268): Show |
276 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(273): Show |
intron_variant | MODIFIER | c.539-2664A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854513 | |||||||
chr16:87854550 | G | T | 1 | a0003c0008t0064g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.539-2701C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854550 | |||||||
chr16:87854597 | T | A | 1 | a0001c0002t0041g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.539-2748A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854597 | |||||||
chr16:87854632 | G | A | 1 | a0001c0001t0067g0323 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.539-2783C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854632 | |||||||
chr16:87854633 | C | T | 1 | a0001c0001t0004g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-2784G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854633 | |||||||
chr16:87854635 | A | C | 1 | a0001c0001t0004g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-2786T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854635 | |||||||
chr16:87854636 | C | A | 1 | a0001c0001t0004g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-2787G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854636 | |||||||
chr16:87854657 | G | A | 1 | a0001c0001t0002g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.539-2808C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854657 | |||||||
chr16:87854696 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.539-2847C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854696 | |||||||
chr16:87854698 | C | G | 1 | a0001c0001t0004g0095 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.539-2849G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854698 | |||||||
chr16:87854707 | C | A | 1 | a0001c0001t0004g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.539-2858G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854707 | |||||||
chr16:87854711 | G | A | 8 | a0001c0001t0010g0266 a0001c0001t0010g0287 a0001c0002t0008g0039 others(5): Show |
8 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.539-2862C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854711 | |||||||
chr16:87854716 | G | A | 5 | a0001c0001t0004g0282 a0001c0001t0018g0312 a0001c0001t0018g0313 others(2): Show |
5 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-2867C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854716 | |||||||
chr16:87854954 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.539-3105C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854954 | |||||||
chr16:87854984 | C | T | 3 | a0001c0001t0005g0063 a0001c0001t0012g0061 a0001c0001t0012g0062 |
3 | HG01109.hp1 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.539-3135G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87854984 | |||||||
chr16:87855012 | C | G | 1 | a0001c0001t0002g0221 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.539-3163G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855012 | |||||||
chr16:87855127 | T | C | 275 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(272): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.539-3278A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855127 | |||||||
chr16:87855130 | G | A | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(256): Show |
262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.539-3281C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855130 | |||||||
chr16:87855137 | G | A | 3 | a0001c0001t0034g0009 a0001c0002t0001g0037 a0003c0014t0035g0008 |
3 | HG02723.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.539-3288C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855137 | |||||||
chr16:87855549 | C | T | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(256): Show |
262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.539-3700G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855549 | |||||||
chr16:87855554 | T | C | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(256): Show |
262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.539-3705A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855554 | |||||||
chr16:87855597 | G | A | 224 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(221): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.539-3748C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855597 | |||||||
chr16:87855806 | C | T | 258 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(255): Show |
261 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.539-3957G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855806 | |||||||
chr16:87855887 | C | T | 255 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(252): Show |
258 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.539-4038G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855887 | |||||||
chr16:87855889 | T | C | 258 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(255): Show |
261 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.539-4040A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855889 | |||||||
chr16:87855954 | G | A | 1 | a0001c0001t0023g0351 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.539-4105C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855954 | |||||||
chr16:87855956 | C | T | 70 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0004g0282 others(67): Show |
73 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.539-4107G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855956 | |||||||
chr16:87855959 | C | T | 40 | a0001c0001t0001g0068 a0001c0001t0001g0148 a0001c0001t0001g0265 others(37): Show |
41 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.539-4110G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855959 | |||||||
chr16:87855962 | T | C | 4 | a0001c0002t0006g0026 a0001c0002t0006g0027 a0001c0002t0006g0029 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-4113A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87855962 | |||||||
chr16:87856020 | CCTGTCTG others(12): Show |
C | 1 | a0001c0001t0047g0185 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.539-4190_539-4172d others(21): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856020 | |||||||
chr16:87856040 | C | T | 27 | a0001c0001t0005g0167 a0001c0001t0006g0069 a0001c0001t0007g0326 others(24): Show |
29 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.539-4191G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856040 | |||||||
chr16:87856108 | C | T | 214 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(211): Show |
216 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.539-4259G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856108 | |||||||
chr16:87856234 | G | A | 40 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0001g0265 others(37): Show |
41 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.539-4385C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856234 | |||||||
chr16:87856236 | G | A | 4 | a0001c0002t0026g0017 a0001c0002t0027g0018 a0001c0002t0027g0019 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-4387C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856236 | |||||||
chr16:87856254 | T | C | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(256): Show |
262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.539-4405A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856254 | |||||||
chr16:87856358 | G | A | 1 | a0001c0013t0012g0166 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.539-4509C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856358 | |||||||
chr16:87856439 | A | G | 4 | a0001c0001t0020g0226 a0001c0001t0065g0371 a0001c0002t0012g0052 others(1): Show |
4 | HG02258.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-4590T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856439 | |||||||
chr16:87856463 | C | T | 1 | a0001c0001t0020g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.539-4614G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856463 | |||||||
chr16:87856512 | C | A | 13 | a0001c0001t0001g0177 a0001c0001t0001g0267 a0001c0001t0001g0268 others(10): Show |
13 | HG00673.hp1 HG00733.hp2 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.539-4663G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856512 | |||||||
chr16:87856646 | G | A | 1 | a0001c0002t0010g0042 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.539-4797C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856646 | |||||||
chr16:87856661 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.539-4812G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856661 | |||||||
chr16:87856824 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.539-4975G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856824 | |||||||
chr16:87856835 | A | G | 108 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0001g0265 others(105): Show |
112 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.539-4986T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856835 | |||||||
chr16:87856849 | G | T | 49 | a0001c0001t0004g0282 a0001c0001t0005g0167 a0001c0001t0006g0165 others(46): Show |
50 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.539-5000C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856849 | |||||||
chr16:87856893 | G | A | 1 | a0001c0002t0041g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.539-5044C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856893 | |||||||
chr16:87856966 | C | T | 3 | a0001c0001t0004g0076 a0001c0001t0004g0173 a0001c0001t0004g0174 |
3 | NA18950.hp1 NA19060.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.539-5117G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87856966 | |||||||
chr16:87857008 | C | CT | 108 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0001g0265 others(105): Show |
112 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.539-5160_539-5159i others(3): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857008 | |||||||
chr16:87857096 | C | T | 2 | a0001c0001t0017g0058 a0001c0001t0017g0094 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.539-5247G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857096 | |||||||
chr16:87857136 | C | T | 31 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0001g0265 others(28): Show |
32 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.539-5287G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857136 | |||||||
chr16:87857225 | AT | A | 68 | a0001c0001t0004g0282 a0001c0001t0005g0167 a0001c0001t0006g0069 others(65): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.539-5377delA | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857225 | |||||||
chr16:87857308 | C | T | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0012g0270 |
3 | HG00673.hp1 HG02015.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.539-5459G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857308 | |||||||
chr16:87857365 | G | A | 1 | a0001c0001t0030g0311 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.539-5516C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857365 | |||||||
chr16:87857455 | G | A | 63 | a0001c0001t0004g0282 a0001c0001t0005g0167 a0001c0001t0006g0069 others(60): Show |
66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.539-5606C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857455 | |||||||
chr16:87857531 | C | T | 4 | a0001c0002t0008g0044 a0002c0004t0019g0046 a0002c0004t0043g0047 others(1): Show |
4 | HG02630.hp2 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-5682G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857531 | |||||||
chr16:87857541 | C | A | 8 | a0001c0001t0020g0226 a0001c0002t0006g0026 a0001c0002t0006g0027 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.539-5692G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857541 | |||||||
chr16:87857563 | G | A | 10 | a0001c0001t0010g0266 a0001c0001t0010g0287 a0001c0001t0073g0382 others(7): Show |
10 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.539-5714C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857563 | |||||||
chr16:87857584 | G | A | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG01433.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.539-5735C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857584 | |||||||
chr16:87857679 | A | G | 63 | a0001c0001t0004g0282 a0001c0001t0005g0167 a0001c0001t0006g0069 others(60): Show |
66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.539-5830T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857679 | |||||||
chr16:87857702 | T | G | 5 | a0001c0001t0067g0323 a0001c0002t0005g0012 a0001c0002t0010g0014 others(2): Show |
5 | HG00639.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-5853A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857702 | |||||||
chr16:87857738 | C | G | 30 | a0001c0001t0001g0148 a0001c0001t0001g0265 a0001c0001t0001g0289 others(27): Show |
31 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.539-5889G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857738 | |||||||
chr16:87857816 | T | G | 4 | a0001c0001t0001g0265 a0001c0001t0003g0334 a0001c0001t0004g0263 others(1): Show |
4 | HG00438.hp1 HG01993.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-5967A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857816 | |||||||
chr16:87857905 | G | A | 68 | a0001c0001t0004g0282 a0001c0001t0005g0167 a0001c0001t0006g0069 others(65): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.539-6056C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857905 | |||||||
chr16:87857907 | G | T | 2 | a0001c0001t0004g0173 a0001c0001t0004g0174 |
2 | NA18950.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.539-6058C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87857907 | |||||||
chr16:87858152 | T | G | 1 | a0001c0001t0021g0252 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.539-6303A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858152 | |||||||
chr16:87858269 | G | A | 106 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0001g0265 others(103): Show |
110 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.539-6420C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858269 | |||||||
chr16:87858286 | A | G | 36 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0001g0265 others(33): Show |
37 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.539-6437T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858286 | |||||||
chr16:87858308 | G | A | 3 | a0001c0001t0005g0063 a0001c0001t0012g0061 a0001c0001t0012g0062 |
3 | HG01109.hp1 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.539-6459C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858308 | |||||||
chr16:87858416 | C | T | 3 | a0001c0001t0005g0063 a0001c0001t0012g0061 a0001c0001t0012g0062 |
3 | HG01109.hp1 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.539-6567G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858416 | |||||||
chr16:87858418 | G | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(259): Show |
265 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.539-6569C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858418 | |||||||
chr16:87858431 | C | T | 1 | a0001c0001t0025g0331 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.539-6582G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858431 | |||||||
chr16:87858570 | C | T | 1 | a0001c0001t0036g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.539-6721G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858570 | |||||||
chr16:87858598 | T | A | 10 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0240 others(7): Show |
10 | HG01123.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.539-6749A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858598 | |||||||
chr16:87858665 | T | C | 325 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(322): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.539-6816A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858665 | |||||||
chr16:87858696 | C | T | 11 | a0001c0001t0004g0282 a0001c0001t0006g0165 a0001c0001t0018g0312 others(8): Show |
11 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.539-6847G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858696 | |||||||
chr16:87858698 | G | A | 1 | a0001c0001t0003g0336 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.539-6849C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858698 | |||||||
chr16:87858723 | C | T | 2 | a0001c0001t0007g0326 a0001c0001t0007g0327 |
2 | NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.539-6874G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858723 | |||||||
chr16:87858798 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.539-6949C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858798 | |||||||
chr16:87858813 | C | T | 36 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0001g0265 others(33): Show |
37 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.539-6964G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858813 | |||||||
chr16:87858848 | G | A | 2 | a0001c0001t0034g0009 a0001c0002t0001g0037 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.539-6999C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858848 | |||||||
chr16:87858885 | C | A | 5 | a0001c0001t0067g0323 a0001c0002t0005g0012 a0001c0002t0010g0014 others(2): Show |
5 | HG00639.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-7036G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858885 | |||||||
chr16:87858970 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0060g0144 |
2 | HG01074.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.539-7121C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87858970 | |||||||
chr16:87859091 | T | C | 1 | a0001c0001t0012g0270 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.539-7242A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859091 | |||||||
chr16:87859196 | G | A | 3 | a0001c0001t0013g0281 a0001c0001t0032g0346 a0001c0001t0032g0347 |
3 | HG00323.hp2 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.539-7347C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859196 | |||||||
chr16:87859197 | G | A | 1 | a0001c0001t0072g0381 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.539-7348C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859197 | |||||||
chr16:87859248 | G | C | 5 | a0001c0001t0006g0165 a0001c0001t0040g0164 a0001c0005t0031g0378 others(2): Show |
5 | HG01081.hp2 HG02109.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-7399C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859248 | |||||||
chr16:87859405 | C | G | 64 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0001g0265 others(61): Show |
67 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.539-7556G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859405 | |||||||
chr16:87859418 | G | A | 1 | a0001c0003t0001g0124 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.539-7569C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859418 | |||||||
chr16:87859504 | G | A | 11 | a0001c0001t0004g0282 a0001c0001t0006g0165 a0001c0001t0018g0312 others(8): Show |
11 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.539-7655C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859504 | |||||||
chr16:87859552 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.539-7703G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859552 | |||||||
chr16:87859576 | G | A | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.539-7727C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859576 | |||||||
chr16:87859754 | C | T | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539-7905G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859754 | |||||||
chr16:87859770 | C | T | 1 | a0001c0001t0011g0330 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.539-7921G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859770 | |||||||
chr16:87859803 | T | G | 1 | a0001c0001t0023g0351 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.539-7954A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859803 | |||||||
chr16:87859913 | A | AAAAAC | 32 | a0001c0001t0002g0077 a0001c0001t0002g0179 a0001c0001t0002g0180 others(29): Show |
33 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.539-8069_539-8065d others(7): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859913 | |||||||
chr16:87859913 | AAAAAC | A | 37 | a0001c0001t0005g0167 a0001c0001t0006g0069 a0001c0001t0007g0326 others(34): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.539-8069_539-8065d others(7): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87859913 | |||||||
chr16:87860145 | C | A | 42 | a0001c0001t0004g0282 a0001c0001t0005g0063 a0001c0001t0006g0165 others(39): Show |
43 | HG00280.hp2 HG00639.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.539-8296G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860145 | |||||||
chr16:87860265 | G | A | 1 | a0001c0002t0016g0034 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.539-8416C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860265 | |||||||
chr16:87860323 | C | A | 10 | a0001c0001t0010g0266 a0001c0001t0010g0287 a0001c0001t0073g0382 others(7): Show |
10 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.539-8474G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860323 | |||||||
chr16:87860325 | CA | C | 8 | a0001c0001t0067g0323 a0001c0002t0005g0012 a0001c0002t0006g0026 others(5): Show |
8 | HG00639.hp2 HG01884.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.539-8477delT | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860325 | |||||||
chr16:87860337 | A | T | 33 | a0001c0001t0001g0148 a0001c0001t0001g0265 a0001c0001t0001g0289 others(30): Show |
34 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.539-8488T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860337 | |||||||
chr16:87860337 | AAAATACA others(7): Show |
A | 2 | a0001c0001t0073g0382 a0001c0002t0045g0035 |
2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.539-8502_539-8489d others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860337 | |||||||
chr16:87860338 | AAATACAC others(4): Show |
A | 5 | a0001c0001t0002g0178 a0001c0001t0008g0297 a0001c0002t0001g0037 others(2): Show |
5 | HG00099.hp2 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-8500_539-8490d others(13): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860338 | |||||||
chr16:87860338 | AAATACAC others(6): Show |
A | 3 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0002t0008g0044 |
3 | NA19043.hp1 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.539-8502_539-8490d others(15): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860338 | |||||||
chr16:87860338 | AAATACAC others(8): Show |
A | 10 | a0001c0001t0006g0069 a0001c0001t0008g0145 a0001c0002t0001g0001 others(7): Show |
12 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.539-8504_539-8490d others(17): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860338 | |||||||
chr16:87860339 | A | T | 47 | a0001c0001t0001g0148 a0001c0001t0001g0265 a0001c0001t0001g0289 others(44): Show |
48 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.539-8490T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860339 | |||||||
chr16:87860341 | T | TAC | 3 | a0001c0001t0001g0177 a0001c0001t0002g0149 a0001c0002t0066g0319 |
3 | HG01192.hp1 HG03669.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.539-8494_539-8493d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | |||||||
chr16:87860341 | T | TACAC | 4 | a0001c0001t0006g0130 a0001c0001t0006g0223 a0001c0001t0009g0082 others(1): Show |
4 | HG01167.hp2 HG02965.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.539-8496_539-8493d others(6): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | |||||||
chr16:87860341 | TAC | T | 19 | a0001c0001t0002g0003 a0001c0001t0002g0084 a0001c0001t0002g0087 others(16): Show |
19 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.539-8494_539-8493d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | |||||||
chr16:87860341 | TACAC | T | 14 | a0001c0001t0001g0068 a0001c0001t0002g0077 a0001c0001t0002g0121 others(11): Show |
14 | HG00280.hp1 HG01123.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.539-8496_539-8493d others(6): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | |||||||
chr16:87860341 | TACACAC | T | 35 | a0001c0001t0001g0072 a0001c0001t0001g0099 a0001c0001t0001g0186 others(32): Show |
35 | HG00597.hp2 HG01192.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.539-8498_539-8493d others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | |||||||
chr16:87860341 | TACACACA others(1): Show |
T | 62 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0093 others(59): Show |
64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.539-8500_539-8493d others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | |||||||
chr16:87860341 | TACACACA others(3): Show |
T | 84 | a0001c0001t0001g0056 a0001c0001t0001g0078 a0001c0001t0001g0102 others(81): Show |
84 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.539-8502_539-8493d others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | |||||||
chr16:87860341 | TACACACA others(5): Show |
T | 31 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0001g0100 others(28): Show |
31 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.539-8504_539-8493d others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | |||||||
chr16:87860341 | TACACACA others(7): Show |
T | 13 | a0001c0001t0001g0126 a0001c0001t0001g0139 a0001c0001t0001g0142 others(10): Show |
13 | HG01106.hp2 HG01168.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.539-8506_539-8493d others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | |||||||
chr16:87860341 | TACACACA others(9): Show |
T | 5 | a0001c0001t0002g0221 a0001c0001t0008g0147 a0001c0002t0039g0050 others(2): Show |
5 | HG01167.hp1 HG02055.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-8508_539-8493d others(18): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | |||||||
chr16:87860341 | TACACACA others(11): Show |
T | 3 | a0001c0002t0006g0002 a0001c0002t0006g0048 a0001c0002t0010g0049 |
4 | HG02486.hp1 HG02717.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.539-8510_539-8493d others(20): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | |||||||
chr16:87860341 | TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0216 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.539-8514_539-8493d others(24): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860341 | |||||||
chr16:87860343 | C | T | 52 | a0001c0001t0001g0148 a0001c0001t0001g0265 a0001c0001t0001g0289 others(49): Show |
53 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.539-8494G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860343 | |||||||
chr16:87860345 | C | T | 36 | a0001c0001t0001g0148 a0001c0001t0001g0265 a0001c0001t0001g0289 others(33): Show |
37 | HG00438.hp1 HG00639.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.539-8496G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860345 | |||||||
chr16:87860347 | C | T | 11 | a0001c0001t0007g0360 a0001c0001t0014g0247 a0001c0001t0020g0226 others(8): Show |
11 | HG00639.hp2 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.539-8498G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860347 | |||||||
chr16:87860349 | C | T | 5 | a0001c0001t0005g0167 a0001c0001t0034g0009 a0001c0001t0062g0352 others(2): Show |
5 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-8500G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860349 | |||||||
chr16:87860351 | C | T | 10 | a0001c0001t0002g0178 a0001c0001t0005g0167 a0001c0001t0008g0297 others(7): Show |
10 | HG00099.hp2 HG00642.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.539-8502G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860351 | |||||||
chr16:87860353 | C | T | 9 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0008g0297 others(6): Show |
9 | HG02630.hp2 HG02723.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.539-8504G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860353 | |||||||
chr16:87860355 | C | T | 14 | a0001c0001t0006g0069 a0001c0001t0007g0326 a0001c0001t0007g0327 others(11): Show |
16 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-8506G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860355 | |||||||
chr16:87860357 | C | T | 13 | a0001c0001t0006g0069 a0001c0001t0008g0145 a0001c0002t0001g0001 others(10): Show |
15 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-8508G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860357 | |||||||
chr16:87860359 | C | T | 1 | a0001c0002t0039g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.539-8510G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860359 | |||||||
chr16:87860361 | C | T | 3 | a0001c0002t0006g0002 a0001c0002t0006g0048 a0001c0002t0010g0049 |
4 | HG02486.hp1 HG02717.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.539-8512G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860361 | |||||||
chr16:87860373 | CACACACA others(21): Show |
C | 1 | a0001c0001t0005g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.538+8484_538+8511d others(30): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860373 | |||||||
chr16:87860377 | CACACACA others(17): Show |
C | 2 | a0001c0001t0012g0061 a0001c0001t0012g0062 |
2 | HG01109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.538+8484_538+8507d others(26): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860377 | |||||||
chr16:87860385 | CACACACA others(9): Show |
C | 1 | a0001c0001t0003g0329 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.538+8484_538+8499d others(18): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860385 | |||||||
chr16:87860387 | CACACACA others(7): Show |
C | 4 | a0001c0001t0002g0103 a0001c0001t0003g0336 a0001c0001t0003g0348 others(1): Show |
4 | HG02683.hp2 HG03492.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+8484_538+8497d others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860387 | |||||||
chr16:87860389 | CACACACA others(5): Show |
C | 14 | a0001c0001t0001g0148 a0001c0001t0001g0265 a0001c0001t0001g0289 others(11): Show |
14 | HG00438.hp1 HG01069.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.538+8484_538+8495d others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860389 | |||||||
chr16:87860391 | CACACACA others(3): Show |
C | 19 | a0001c0001t0001g0138 a0001c0001t0002g0137 a0001c0001t0003g0007 others(16): Show |
19 | HG00280.hp2 HG00609.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.538+8484_538+8493d others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860391 | |||||||
chr16:87860393 | CACACACA others(1): Show |
C | 3 | a0001c0001t0003g0007 a0001c0002t0026g0017 a0001c0013t0012g0166 |
3 | HG01256.hp1 HG02572.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.538+8484_538+8491d others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860393 | |||||||
chr16:87860393 | CACACACA others(3): Show |
C | 4 | a0001c0001t0003g0357 a0001c0001t0024g0355 a0001c0001t0024g0356 others(1): Show |
4 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+8482_538+8491d others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860393 | |||||||
chr16:87860395 | C | T | 1 | a0001c0001t0005g0167 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.538+8490G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860395 | |||||||
chr16:87860395 | CACACAT | C | 3 | a0001c0002t0005g0012 a0001c0002t0010g0014 a0001c0002t0012g0052 |
3 | HG00639.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.538+8484_538+8489d others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860395 | |||||||
chr16:87860397 | C | T | 12 | a0001c0001t0002g0088 a0001c0001t0005g0167 a0001c0001t0010g0266 others(9): Show |
12 | HG00642.hp1 HG02630.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.538+8488G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860397 | |||||||
chr16:87860399 | C | CAT | 3 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0051g0090 |
4 | HG01884.hp1 HG02129.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+8484_538+8485d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860399 | |||||||
chr16:87860399 | C | T | 48 | a0001c0001t0002g0088 a0001c0001t0002g0183 a0001c0001t0004g0174 others(45): Show |
50 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.538+8486G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860399 | |||||||
chr16:87860401 | T | C | 1 | a0001c0001t0026g0127 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.538+8484A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860401 | |||||||
chr16:87860409 | T | A | 1 | a0001c0001t0024g0361 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.538+8476A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860409 | |||||||
chr16:87860437 | C | T | 42 | a0001c0001t0001g0148 a0001c0001t0001g0265 a0001c0001t0001g0289 others(39): Show |
43 | HG00438.hp1 HG00639.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.538+8448G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860437 | |||||||
chr16:87860485 | G | A | 2 | a0001c0001t0007g0339 a0001c0001t0007g0349 |
2 | NA18983.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.538+8400C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860485 | |||||||
chr16:87860560 | TCCAGCTG others(4): Show |
T | 8 | a0001c0002t0005g0051 a0001c0002t0006g0002 a0001c0002t0006g0048 others(5): Show |
9 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+8314_538+8324d others(13): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860560 | |||||||
chr16:87860767 | G | A | 5 | a0001c0001t0067g0323 a0001c0002t0005g0012 a0001c0002t0010g0014 others(2): Show |
5 | HG00639.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+8118C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860767 | |||||||
chr16:87860773 | C | T | 1 | a0001c0001t0014g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.538+8112G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860773 | |||||||
chr16:87860903 | G | C | 1 | a0001c0001t0021g0258 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.538+7982C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860903 | |||||||
chr16:87860930 | C | T | 2 | a0001c0001t0073g0382 a0001c0002t0045g0035 |
2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.538+7955G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860930 | |||||||
chr16:87860950 | C | T | 12 | a0001c0001t0001g0177 a0001c0001t0001g0267 a0001c0001t0001g0268 others(9): Show |
12 | HG00673.hp1 HG00733.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.538+7935G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860950 | |||||||
chr16:87860955 | G | A | 5 | a0001c0001t0002g0259 a0001c0001t0002g0260 a0001c0001t0002g0261 others(2): Show |
5 | HG00738.hp1 HG01978.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.538+7930C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860955 | |||||||
chr16:87860986 | C | T | 8 | a0001c0002t0005g0051 a0001c0002t0006g0002 a0001c0002t0006g0048 others(5): Show |
9 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+7899G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87860986 | |||||||
chr16:87861055 | G | C | 2 | a0001c0001t0003g0375 a0001c0001t0013g0160 |
2 | HG01168.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.538+7830C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861055 | |||||||
chr16:87861085 | G | A | 5 | a0001c0001t0067g0323 a0001c0002t0005g0012 a0001c0002t0010g0014 others(2): Show |
5 | HG00639.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+7800C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861085 | |||||||
chr16:87861116 | G | C | 31 | a0001c0001t0005g0167 a0001c0001t0006g0069 a0001c0001t0006g0165 others(28): Show |
33 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.538+7769C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861116 | |||||||
chr16:87861151 | G | A | 1 | a0001c0001t0003g0369 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.538+7734C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861151 | |||||||
chr16:87861215 | G | A | 1 | a0001c0001t0005g0125 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.538+7670C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861215 | |||||||
chr16:87861255 | G | A | 1 | a0001c0002t0001g0001 | 3 | HG01069.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.538+7630C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861255 | |||||||
chr16:87861448 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.538+7437C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861448 | |||||||
chr16:87861493 | G | A | 1 | a0001c0002t0005g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.538+7392C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861493 | |||||||
chr16:87861500 | C | A | 1 | a0001c0001t0067g0323 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538+7385G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861500 | |||||||
chr16:87861565 | GGCCAAGA others(14): Show |
G | 1 | a0001c0001t0002g0221 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.538+7299_538+7319d others(23): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861565 | |||||||
chr16:87861680 | C | G | 5 | a0001c0001t0005g0063 a0001c0001t0012g0061 a0001c0001t0012g0062 others(2): Show |
5 | HG01109.hp1 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+7205G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861680 | |||||||
chr16:87861838 | C | G | 3 | a0001c0001t0005g0170 a0001c0001t0005g0171 a0001c0001t0005g0172 |
3 | HG01175.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.538+7047G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861838 | |||||||
chr16:87861888 | C | T | 2 | a0001c0005t0031g0378 a0001c0005t0031g0380 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.538+6997G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861888 | |||||||
chr16:87861930 | A | G | 1 | a0001c0002t0066g0319 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.538+6955T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87861930 | |||||||
chr16:87862216 | C | T | 4 | a0001c0002t0026g0017 a0001c0002t0027g0018 a0001c0002t0027g0019 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+6669G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862216 | |||||||
chr16:87862228 | T | G | 5 | a0001c0002t0006g0026 a0001c0002t0006g0027 a0001c0002t0006g0028 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+6657A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862228 | |||||||
chr16:87862253 | T | C | 5 | a0001c0001t0067g0323 a0001c0002t0005g0012 a0001c0002t0010g0014 others(2): Show |
5 | HG00639.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+6632A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862253 | |||||||
chr16:87862415 | G | A | 3 | a0004c0006t0008g0308 a0004c0006t0008g0309 a0004c0006t0014g0307 |
3 | HG02615.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.538+6470C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862415 | |||||||
chr16:87862443 | A | G | 3 | a0001c0001t0001g0075 a0001c0001t0004g0074 a0006c0007t0001g0010 |
3 | HG01978.hp1 HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.538+6442T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862443 | |||||||
chr16:87862454 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.538+6431A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862454 | |||||||
chr16:87862639 | G | C | 7 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0286 others(4): Show |
7 | HG01167.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.538+6246C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862639 | |||||||
chr16:87862851 | T | C | 3 | a0001c0001t0005g0063 a0001c0001t0012g0061 a0001c0001t0012g0062 |
3 | HG01109.hp1 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.538+6034A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862851 | |||||||
chr16:87862992 | C | T | 1 | a0001c0001t0022g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.538+5893G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87862992 | |||||||
chr16:87863010 | G | A | 1 | a0004c0006t0008g0309 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.538+5875C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863010 | |||||||
chr16:87863130 | C | T | 1 | a0001c0001t0033g0353 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.538+5755G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863130 | |||||||
chr16:87863131 | G | A | 25 | a0001c0001t0004g0282 a0001c0001t0010g0266 a0001c0001t0010g0287 others(22): Show |
26 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.538+5754C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863131 | |||||||
chr16:87863272 | T | C | 1 | a0001c0002t0012g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.538+5613A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863272 | |||||||
chr16:87863354 | G | A | 2 | a0001c0001t0002g0301 a0001c0001t0009g0222 |
2 | HG02738.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.538+5531C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863354 | |||||||
chr16:87863443 | C | T | 1 | a0001c0001t0003g0329 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.538+5442G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863443 | |||||||
chr16:87863452 | A | T | 6 | a0001c0001t0014g0055 a0001c0001t0014g0247 a0001c0001t0014g0248 others(3): Show |
6 | HG02897.hp2 HG02970.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.538+5433T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863452 | |||||||
chr16:87863610 | G | A | 1 | a0001c0001t0006g0223 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.538+5275C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863610 | |||||||
chr16:87863731 | G | A | 8 | a0001c0002t0005g0051 a0001c0002t0006g0002 a0001c0002t0006g0048 others(5): Show |
9 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+5154C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863731 | |||||||
chr16:87863788 | C | G | 1 | a0001c0001t0001g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.538+5097G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863788 | |||||||
chr16:87863792 | C | T | 1 | a0001c0002t0020g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.538+5093G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863792 | |||||||
chr16:87863872 | G | A | 3 | a0001c0005t0031g0378 a0001c0005t0031g0380 a0001c0005t0063g0379 |
3 | HG01081.hp2 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.538+5013C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863872 | |||||||
chr16:87863892 | T | C | 1 | a0001c0001t0049g0161 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.538+4993A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863892 | |||||||
chr16:87863913 | A | C | 1 | a0001c0001t0001g0168 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.538+4972T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863913 | |||||||
chr16:87863967 | TTATGTGT others(25): Show |
T | 1 | a0001c0003t0001g0073 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.538+4886_538+4917d others(34): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863967 | |||||||
chr16:87863982 | T | TAAAAAA | 8 | a0001c0001t0010g0266 a0001c0001t0010g0287 a0001c0002t0008g0039 others(5): Show |
8 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.538+4902_538+4903i others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863982 | |||||||
chr16:87863984 | A | ATATATAT others(8): Show |
1 | a0001c0001t0003g0345 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.538+4900_538+4901i others(17): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863984 | |||||||
chr16:87863986 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.538+4898_538+4899i others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AAAAAAAA others(11): Show |
6 | a0001c0001t0004g0282 a0001c0001t0018g0312 a0001c0001t0018g0313 others(3): Show |
6 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.538+4898_538+4899i others(20): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AAAATATA others(11): Show |
1 | a0001c0001t0005g0080 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.538+4898_538+4899i others(20): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AAAATATA others(13): Show |
1 | a0001c0013t0012g0166 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.538+4898_538+4899i others(22): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AAT | 8 | a0001c0002t0005g0051 a0001c0002t0006g0002 a0001c0002t0006g0048 others(5): Show |
9 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+4897_538+4898d others(4): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATACATA others(5): Show |
3 | a0001c0001t0001g0265 a0001c0001t0004g0263 a0001c0001t0004g0264 |
3 | HG00438.hp1 HG02165.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.538+4898_538+4899i others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATAT | 4 | a0001c0002t0012g0052 a0001c0002t0026g0017 a0001c0002t0027g0018 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+4895_538+4898d others(6): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATAT | 9 | a0001c0001t0006g0069 a0001c0001t0006g0165 a0001c0001t0008g0145 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+4893_538+4898d others(8): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(1): Show |
8 | a0001c0001t0005g0063 a0001c0001t0011g0374 a0001c0001t0012g0061 others(5): Show |
8 | HG01109.hp1 HG01516.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.538+4891_538+4898d others(10): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(3): Show |
15 | a0001c0001t0014g0055 a0001c0001t0014g0247 a0001c0001t0014g0248 others(12): Show |
17 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.538+4889_538+4898d others(12): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(5): Show |
89 | a0001c0001t0001g0006 a0001c0001t0001g0108 a0001c0001t0001g0116 others(86): Show |
91 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.538+4887_538+4898d others(14): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(7): Show |
43 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0068 others(40): Show |
44 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.538+4885_538+4898d others(16): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(9): Show |
43 | a0001c0001t0001g0072 a0001c0001t0001g0100 a0001c0001t0001g0186 others(40): Show |
43 | HG00673.hp1 HG00733.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.538+4883_538+4898d others(18): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(11): Show |
48 | a0001c0001t0001g0099 a0001c0001t0001g0104 a0001c0001t0001g0154 others(45): Show |
48 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.538+4881_538+4898d others(20): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(13): Show |
31 | a0001c0001t0001g0071 a0001c0001t0001g0078 a0001c0001t0001g0213 others(28): Show |
31 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.538+4879_538+4898d others(22): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(15): Show |
17 | a0001c0001t0001g0153 a0001c0001t0002g0005 a0001c0001t0002g0278 others(14): Show |
17 | HG00140.hp1 HG01081.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.538+4877_538+4898d others(24): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(17): Show |
11 | a0001c0001t0002g0003 a0001c0001t0002g0070 a0001c0001t0002g0149 others(8): Show |
11 | HG00738.hp1 HG01192.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.538+4898_538+4899i others(26): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(19): Show |
10 | a0001c0001t0002g0003 a0001c0001t0002g0083 a0001c0001t0002g0084 others(7): Show |
10 | HG00741.hp2 HG01099.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.538+4898_538+4899i others(28): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(21): Show |
4 | a0001c0001t0002g0283 a0001c0001t0003g0367 a0001c0001t0030g0310 others(1): Show |
4 | HG00280.hp1 HG01074.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+4898_538+4899i others(30): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(23): Show |
3 | a0001c0001t0001g0085 a0001c0001t0001g0102 a0001c0001t0002g0259 |
3 | HG01993.hp2 HG02683.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.538+4898_538+4899i others(32): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(25): Show |
4 | a0001c0001t0007g0343 a0001c0001t0007g0344 a0001c0001t0013g0218 others(1): Show |
4 | HG00639.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+4898_538+4899i others(34): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(27): Show |
1 | a0005c0012t0002g0292 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.538+4898_538+4899i others(36): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(33): Show |
1 | a0001c0001t0007g0328 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.538+4898_538+4899i others(42): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(37): Show |
3 | a0001c0001t0001g0093 a0001c0001t0007g0341 a0001c0001t0007g0342 |
3 | HG02071.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.538+4898_538+4899i others(46): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | AATATATA others(39): Show |
1 | a0001c0001t0002g0134 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.538+4898_538+4899i others(48): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0142 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.538+4898_538+4899i others(15): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0332 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.538+4898_538+4899i others(23): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863986 | A | T | 1 | a0001c0001t0003g0345 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.538+4899T>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863986 | |||||||
chr16:87863998 | T | C | 6 | a0001c0001t0004g0282 a0001c0001t0018g0312 a0001c0001t0018g0313 others(3): Show |
6 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.538+4887A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87863998 | |||||||
chr16:87864020 | G | A | 2 | a0001c0002t0023g0316 a0001c0002t0023g0317 |
2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.538+4865C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864020 | |||||||
chr16:87864030 | G | A | 4 | a0001c0001t0025g0350 a0001c0002t0005g0012 a0001c0002t0010g0014 others(1): Show |
4 | HG00639.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+4855C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864030 | |||||||
chr16:87864108 | G | A | 1 | a0001c0001t0006g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.538+4777C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864108 | |||||||
chr16:87864269 | A | G | 64 | a0001c0001t0004g0282 a0001c0001t0005g0063 a0001c0001t0005g0167 others(61): Show |
67 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.538+4616T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864269 | |||||||
chr16:87864279 | C | A | 2 | a0001c0001t0029g0162 a0001c0001t0029g0163 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.538+4606G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864279 | |||||||
chr16:87864435 | G | A | 9 | a0001c0001t0010g0266 a0001c0001t0010g0287 a0001c0002t0008g0039 others(6): Show |
9 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+4450C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864435 | |||||||
chr16:87864571 | A | C | 7 | a0001c0002t0005g0012 a0001c0002t0010g0014 a0001c0002t0012g0052 others(4): Show |
7 | HG00639.hp2 HG01081.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+4314T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864571 | |||||||
chr16:87864598 | T | C | 19 | a0001c0001t0001g0128 a0001c0001t0001g0229 a0001c0001t0001g0230 others(16): Show |
19 | HG00408.hp1 HG00544.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.538+4287A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864598 | |||||||
chr16:87864754 | A | G | 1 | a0001c0001t0003g0340 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.538+4131T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864754 | |||||||
chr16:87864886 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.538+3999T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864886 | |||||||
chr16:87864935 | G | A | 4 | a0001c0001t0006g0130 a0001c0001t0006g0131 a0001c0001t0006g0132 others(1): Show |
4 | HG01243.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+3950C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864935 | |||||||
chr16:87864990 | C | G | 1 | a0001c0002t0020g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.538+3895G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87864990 | |||||||
chr16:87865144 | T | C | 1 | a0001c0001t0062g0352 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.538+3741A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865144 | |||||||
chr16:87865327 | C | T | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG01070.hp2 HG01071.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.538+3558G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865327 | |||||||
chr16:87865436 | T | C | 62 | a0001c0001t0004g0282 a0001c0001t0005g0063 a0001c0001t0006g0069 others(59): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.538+3449A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865436 | |||||||
chr16:87865480 | G | A | 2 | a0001c0005t0031g0378 a0001c0005t0031g0380 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.538+3405C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865480 | |||||||
chr16:87865621 | C | T | 1 | a0001c0005t0031g0378 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.538+3264G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865621 | |||||||
chr16:87865663 | T | C | 34 | a0001c0001t0006g0069 a0001c0001t0006g0165 a0001c0001t0008g0145 others(31): Show |
37 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.538+3222A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865663 | |||||||
chr16:87865708 | G | C | 8 | a0001c0001t0020g0226 a0001c0002t0006g0026 a0001c0002t0006g0027 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.538+3177C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865708 | |||||||
chr16:87865732 | T | A | 8 | a0001c0001t0020g0226 a0001c0002t0006g0026 a0001c0002t0006g0027 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.538+3153A>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865732 | |||||||
chr16:87865787 | T | G | 3 | a0001c0001t0034g0009 a0001c0002t0001g0037 a0003c0014t0035g0008 |
3 | HG02723.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.538+3098A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865787 | |||||||
chr16:87865832 | C | G | 11 | a0001c0001t0020g0226 a0001c0001t0034g0009 a0001c0002t0001g0037 others(8): Show |
11 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.538+3053G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865832 | |||||||
chr16:87865846 | G | A | 3 | a0001c0001t0034g0009 a0001c0002t0001g0037 a0003c0014t0035g0008 |
3 | HG02723.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.538+3039C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865846 | |||||||
chr16:87865849 | C | T | 1 | a0001c0013t0012g0166 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.538+3036G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865849 | |||||||
chr16:87865878 | T | C | 1 | a0001c0001t0004g0225 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.538+3007A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865878 | |||||||
chr16:87865892 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.538+2993G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865892 | |||||||
chr16:87865901 | G | A | 2 | a0001c0001t0006g0165 a0001c0001t0040g0164 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.538+2984C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865901 | |||||||
chr16:87865963 | G | A | 1 | a0001c0001t0067g0323 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538+2922C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865963 | |||||||
chr16:87865979 | G | C | 36 | a0001c0001t0001g0265 a0001c0001t0001g0289 a0001c0001t0003g0007 others(33): Show |
37 | HG00438.hp1 HG00438.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.538+2906C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87865979 | |||||||
chr16:87866015 | A | G | 10 | a0001c0001t0020g0226 a0001c0002t0006g0026 a0001c0002t0006g0027 others(7): Show |
10 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.538+2870T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866015 | |||||||
chr16:87866091 | T | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0148 a0001c0001t0001g0150 others(83): Show |
90 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.538+2794A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866091 | |||||||
chr16:87866097 | G | C | 3 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 |
3 | NA18977.hp1 NA19009.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.538+2788C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866097 | |||||||
chr16:87866110 | T | G | 147 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0138 others(144): Show |
152 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.538+2775A>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866110 | |||||||
chr16:87866266 | G | A | 11 | a0001c0002t0001g0016 a0001c0002t0001g0021 a0001c0002t0001g0022 others(8): Show |
11 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.538+2619C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866266 | |||||||
chr16:87866267 | G | C | 7 | a0001c0002t0006g0026 a0001c0002t0006g0027 a0001c0002t0006g0028 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+2618C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866267 | |||||||
chr16:87866272 | C | T | 7 | a0001c0002t0006g0002 a0001c0002t0006g0048 a0001c0002t0010g0049 others(4): Show |
8 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.538+2613G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866272 | |||||||
chr16:87866300 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.538+2585C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866300 | |||||||
chr16:87866305 | A | G | 2 | a0001c0001t0011g0324 a0001c0001t0025g0325 |
2 | HG01070.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.538+2580T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866305 | |||||||
chr16:87866334 | G | C | 7 | a0001c0001t0010g0287 a0001c0001t0016g0284 a0001c0001t0016g0285 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+2551C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866334 | |||||||
chr16:87866383 | T | C | 153 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0068 others(150): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.538+2502A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866383 | |||||||
chr16:87866436 | G | A | 21 | a0001c0001t0001g0265 a0001c0001t0004g0263 a0001c0001t0004g0264 others(18): Show |
21 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.538+2449C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866436 | |||||||
chr16:87866478 | T | C | 10 | a0001c0001t0010g0266 a0001c0002t0001g0037 a0001c0002t0008g0039 others(7): Show |
10 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.538+2407A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866478 | |||||||
chr16:87866489 | G | A | 1 | a0001c0001t0065g0371 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.538+2396C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866489 | |||||||
chr16:87866496 | C | T | 1 | a0001c0001t0067g0323 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538+2389G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866496 | |||||||
chr16:87866503 | T | C | 2 | a0001c0001t0034g0009 a0003c0014t0035g0008 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.538+2382A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866503 | |||||||
chr16:87866506 | C | T | 9 | a0001c0002t0001g0037 a0001c0002t0008g0039 a0001c0002t0008g0040 others(6): Show |
9 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+2379G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866506 | |||||||
chr16:87866596 | G | C | 7 | a0001c0001t0010g0287 a0001c0001t0016g0284 a0001c0001t0016g0285 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+2289C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866596 | |||||||
chr16:87866647 | A | G | 1 | a0001c0001t0073g0382 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.538+2238T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866647 | |||||||
chr16:87866686 | C | T | 6 | a0001c0001t0010g0287 a0001c0001t0016g0284 a0001c0001t0016g0285 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.538+2199G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866686 | |||||||
chr16:87866692 | C | T | 1 | a0001c0002t0045g0035 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.538+2193G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866692 | |||||||
chr16:87866763 | G | C | 22 | a0001c0002t0001g0016 a0001c0002t0001g0021 a0001c0002t0001g0022 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.538+2122C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866763 | |||||||
chr16:87866842 | C | A | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.538+2043G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866842 | |||||||
chr16:87866919 | G | C | 16 | a0001c0002t0001g0016 a0001c0002t0001g0021 a0001c0002t0001g0022 others(13): Show |
16 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.538+1966C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866919 | |||||||
chr16:87866934 | G | A | 9 | a0001c0002t0001g0001 a0001c0002t0005g0051 a0001c0002t0006g0002 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.538+1951C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866934 | |||||||
chr16:87866957 | A | G | 9 | a0001c0002t0001g0037 a0001c0002t0008g0039 a0001c0002t0008g0040 others(6): Show |
9 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+1928T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866957 | |||||||
chr16:87866994 | G | C | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0006g0269 others(1): Show |
4 | HG00673.hp1 HG02015.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+1891C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87866994 | |||||||
chr16:87867020 | A | G | 367 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0056 others(364): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.538+1865T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867020 | |||||||
chr16:87867033 | C | T | 1 | a0001c0001t0067g0323 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538+1852G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867033 | |||||||
chr16:87867071 | C | T | 9 | a0001c0002t0001g0001 a0001c0002t0005g0051 a0001c0002t0006g0002 others(6): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.538+1814G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867071 | |||||||
chr16:87867172 | G | A | 1 | a0001c0001t0016g0288 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.538+1713C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867172 | |||||||
chr16:87867200 | G | A | 23 | a0001c0002t0001g0016 a0001c0002t0001g0021 a0001c0002t0001g0022 others(20): Show |
23 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.538+1685C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867200 | |||||||
chr16:87867218 | C | A | 1 | a0001c0001t0036g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.538+1667G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867218 | |||||||
chr16:87867218 | C | T | 4 | a0001c0002t0008g0044 a0002c0004t0019g0046 a0002c0004t0043g0047 others(1): Show |
4 | HG02630.hp2 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+1667G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867218 | |||||||
chr16:87867254 | G | A | 6 | a0001c0001t0010g0287 a0001c0001t0016g0284 a0001c0001t0016g0285 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.538+1631C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867254 | |||||||
chr16:87867268 | C | T | 23 | a0001c0002t0001g0016 a0001c0002t0001g0021 a0001c0002t0001g0022 others(20): Show |
23 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.538+1617G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867268 | |||||||
chr16:87867303 | C | G | 1 | a0001c0001t0014g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.538+1582G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867303 | |||||||
chr16:87867306 | G | A | 7 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(4): Show |
7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+1579C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867306 | |||||||
chr16:87867309 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.538+1576C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867309 | |||||||
chr16:87867385 | C | A | 63 | a0001c0001t0001g0289 a0001c0001t0003g0007 a0001c0001t0003g0329 others(60): Show |
64 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.538+1500G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867385 | |||||||
chr16:87867429 | C | A | 1 | a0001c0001t0004g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.538+1456G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867429 | |||||||
chr16:87867472 | A | G | 86 | a0001c0001t0001g0289 a0001c0001t0003g0007 a0001c0001t0003g0329 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.538+1413T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867472 | |||||||
chr16:87867549 | C | G | 3 | a0001c0005t0031g0378 a0001c0005t0031g0380 a0001c0005t0063g0379 |
3 | HG01081.hp2 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.538+1336G>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867549 | |||||||
chr16:87867564 | C | T | 1 | a0001c0002t0055g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.538+1321G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867564 | |||||||
chr16:87867595 | C | T | 1 | a0001c0001t0006g0069 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.538+1290G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867595 | |||||||
chr16:87867681 | T | C | 7 | a0001c0001t0003g0367 a0001c0001t0003g0368 a0001c0001t0003g0369 others(4): Show |
7 | HG00438.hp2 HG02132.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+1204A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867681 | |||||||
chr16:87867703 | G | C | 85 | a0001c0001t0001g0289 a0001c0001t0003g0007 a0001c0001t0003g0329 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.538+1182C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867703 | |||||||
chr16:87867840 | G | A | 22 | a0001c0002t0001g0016 a0001c0002t0001g0021 a0001c0002t0001g0022 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.538+1045C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867840 | |||||||
chr16:87867853 | C | A | 2 | a0001c0001t0001g0304 a0001c0001t0004g0290 |
2 | HG02015.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.538+1032G>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867853 | |||||||
chr16:87867886 | C | T | 1 | a0001c0002t0001g0001 | 3 | HG01069.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.538+999G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87867886 | |||||||
chr16:87868057 | G | A | 123 | a0001c0001t0003g0007 a0001c0001t0003g0329 a0001c0001t0003g0332 others(120): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.538+828C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868057 | |||||||
chr16:87868104 | G | A | 51 | a0001c0002t0001g0001 a0001c0002t0001g0016 a0001c0002t0001g0021 others(48): Show |
54 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.538+781C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868104 | |||||||
chr16:87868115 | C | CA | 75 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0296 others(72): Show |
76 | HG00323.hp2 HG00673.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.538+769dupT | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868115 | |||||||
chr16:87868115 | C | CAA | 6 | a0001c0001t0005g0063 a0001c0001t0011g0372 a0001c0001t0011g0373 others(3): Show |
6 | HG00438.hp2 HG01109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.538+768_538+769dup others(2): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868115 | |||||||
chr16:87868129 | A | G | 1 | a0001c0002t0010g0043 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.538+756T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868129 | |||||||
chr16:87868130 | A | G | 47 | a0001c0001t0001g0068 a0001c0001t0015g0065 a0001c0001t0015g0066 others(44): Show |
50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.538+755T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868130 | |||||||
chr16:87868132 | A | G | 7 | a0001c0002t0006g0026 a0001c0002t0006g0027 a0001c0002t0006g0028 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+753T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868132 | |||||||
chr16:87868132 | AAG | A | 43 | a0001c0002t0001g0001 a0001c0002t0001g0016 a0001c0002t0001g0021 others(40): Show |
46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.538+751_538+752del others(2): Show |
SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868132 | |||||||
chr16:87868134 | G | A | 7 | a0001c0002t0006g0026 a0001c0002t0006g0027 a0001c0002t0006g0028 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+751C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868134 | |||||||
chr16:87868157 | A | G | 1 | a0001c0001t0036g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.538+728T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868157 | |||||||
chr16:87868258 | G | A | 1 | a0001c0002t0055g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.538+627C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868258 | |||||||
chr16:87868278 | A | C | 51 | a0001c0002t0001g0001 a0001c0002t0001g0016 a0001c0002t0001g0021 others(48): Show |
54 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.538+607T>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868278 | |||||||
chr16:87868320 | G | C | 10 | a0001c0002t0001g0037 a0001c0002t0008g0039 a0001c0002t0008g0040 others(7): Show |
10 | HG02630.hp1 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.538+565C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868320 | |||||||
chr16:87868350 | T | C | 51 | a0001c0002t0001g0001 a0001c0002t0001g0016 a0001c0002t0001g0021 others(48): Show |
54 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.538+535A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868350 | |||||||
chr16:87868361 | C | T | 1 | a0001c0001t0050g0060 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.538+524G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868361 | |||||||
chr16:87868378 | G | T | 37 | a0001c0002t0001g0016 a0001c0002t0001g0021 a0001c0002t0001g0022 others(34): Show |
37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.538+507C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868378 | |||||||
chr16:87868400 | G | A | 1 | a0001c0001t0011g0374 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.538+485C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868400 | |||||||
chr16:87868402 | G | C | 51 | a0001c0002t0001g0001 a0001c0002t0001g0016 a0001c0002t0001g0021 others(48): Show |
54 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.538+483C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868402 | |||||||
chr16:87868503 | G | A | 7 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(4): Show |
7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+382C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868503 | |||||||
chr16:87868510 | T | C | 1 | a0001c0001t0006g0305 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.538+375A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868510 | |||||||
chr16:87868542 | T | C | 1 | a0001c0001t0003g0375 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.538+343A>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868542 | |||||||
chr16:87868593 | G | C | 118 | a0001c0001t0003g0007 a0001c0001t0003g0329 a0001c0001t0003g0332 others(115): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.538+292C>G | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868593 | |||||||
chr16:87868606 | A | G | 117 | a0001c0001t0003g0007 a0001c0001t0003g0329 a0001c0001t0003g0332 others(114): Show |
121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.538+279T>C | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868606 | |||||||
chr16:87868610 | C | T | 1 | a0003c0015t0042g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.538+275G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868610 | |||||||
chr16:87868649 | G | T | 1 | a0001c0001t0017g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.538+236C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868649 | |||||||
chr16:87868654 | G | A | 7 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(4): Show |
7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+231C>T | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868654 | |||||||
chr16:87868721 | G | T | 1 | a0001c0001t0004g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.538+164C>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868721 | |||||||
chr16:87868737 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.538+148G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868737 | |||||||
chr16:87868767 | C | T | 1 | a0001c0001t0014g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.538+118G>A | SLC7A5 | ENSG00000103257.9 | transcript | ENST00000261622.5 | protein_coding | 1/9 | chr16 | 87868767 |