Item | Value |
---|---|
geneid | 5172 |
ensemblid | ENSG00000091137.14 |
hgncid | 8818 |
symbol | SLC26A4 |
name | solute carrier family 26 member 4 |
refseq_nuc | NM_000441.2 |
refseq_prot | NP_000432.1 |
ensembl_nuc | ENST00000644269.2 |
ensembl_prot | ENSP00000494017.1 |
mane_status | MANE Select |
chr | chr7 |
start | 107660828 |
end | 107717809 |
strand | + |
ver | v1.2 |
region | chr7:107660828-107717809 |
region5000 | chr7:107655828-107722809 |
regionname0 | SLC26A4_chr7_107660828_107717809 |
regionname5000 | SLC26A4_chr7_107655828_107722809 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 780 | 336 | 72 | 70 | 146 | 16 | 30 | 111 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0002 | 0/0 | 780 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0003 | 0/0 | 780 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0004 | 0/0 | 780 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0005 | 0/0 | 780 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0006 | 0/0 | 780 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0007 | 0/0 | 780 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0008 | 0/0 | 780 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0009 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0010 | 0/0 | 780 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0011 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0012 | 0/0 | 780 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0013 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0014 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0015 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
a0016 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | MAAPG others(775): Show |
chr7 | 107655828 | 107722809 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2340 | 329 | 67 | 70 | 145 | 16 | 29 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0001c0006 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0001c0011 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0001c0012 | 0/0 | 2340 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0001c0019 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0001c0022 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0002c0002 | 0/0 | 2340 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0002c0009 | 0/0 | 2340 | 2 | 1 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0003c0003 | 0/0 | 2340 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0004c0004 | 0/0 | 2340 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0005c0005 | 0/0 | 2340 | 3 | 0 | 0 | 0 | 0 | 3 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0006c0008 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0007c0010 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0008c0007 | 0/0 | 2340 | 2 | 0 | 0 | 0 | 0 | 2 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0009c0021 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0010c0013 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0011c0017 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0012c0020 | 0/0 | 2340 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0013c0015 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0014c0014 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0015c0016 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 | ||
a0016c0018 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATGGC others(2335): Show |
chr7 | 107655828 | 107722809 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4735 | 147 | 28 | 27 | 75 | 6 | 11 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0002 | 0/0 | 4734 | 73 | 1 | 17 | 41 | 4 | 10 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0003 | 1/0 | 4737 | 32 | 12 | 11 | 1 | 2 | 5 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0004 | 0/0 | 4735 | 15 | 2 | 2 | 11 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0005 | 0/0 | 4736 | 12 | 1 | 4 | 4 | 2 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4731): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0006 | 0/0 | 4734 | 8 | 1 | 3 | 2 | 1 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0007 | 0/0 | 4734 | 5 | 5 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0008 | 0/0 | 4738 | 7 | 4 | 2 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4733): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0009 | 0/0 | 4737 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0010 | 0/0 | 4737 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0011 | 0/0 | 4734 | 3 | 0 | 0 | 3 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0012 | 0/0 | 4737 | 3 | 1 | 0 | 1 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0013 | 0/0 | 4735 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0015 | 0/0 | 4735 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0016 | 0/0 | 4734 | 2 | 1 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0017 | 0/0 | 4737 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0019 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0020 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0021 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0022 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0023 | 0/0 | 4735 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0026 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0027 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0028 | 0/0 | 4722 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4717): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0029 | 0/1 | 4737 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0001c0001t0031 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0001c0006t0001 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0001c0006t0006 | 0/0 | 4734 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
a0001c0011t0007 | 0/0 | 4734 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
a0001c0012t0001 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0001c0019t0001 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0001c0022t0006 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
a0002c0002t0013 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0002c0002t0014 | 0/0 | 4735 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0002c0002t0018 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0002c0009t0024 | 0/0 | 4738 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4733): Show |
chr7 | 107655828 | 107722809 |
a0002c0009t0025 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0003c0003t0003 | 0/0 | 4737 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0004c0004t0009 | 0/0 | 4737 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0005c0005t0001 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0005c0005t0002 | 0/0 | 4734 | 2 | 0 | 0 | 0 | 0 | 2 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
a0006c0008t0014 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0006c0008t0030 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0007c0010t0003 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0007c0010t0005 | 0/0 | 4736 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4731): Show |
chr7 | 107655828 | 107722809 |
a0008c0007t0003 | 0/0 | 4737 | 2 | 0 | 0 | 0 | 0 | 2 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4732): Show |
chr7 | 107655828 | 107722809 |
a0009c0021t0001 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0010c0013t0006 | 0/0 | 4734 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
a0011c0017t0001 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0012c0020t0001 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0013c0015t0018 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0014c0014t0001 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4730): Show |
chr7 | 107655828 | 107722809 |
a0015c0016t0011 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
a0016c0018t0002 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | ATTCC others(4729): Show |
chr7 | 107655828 | 107722809 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0007g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0009g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0010g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0010g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0011g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0011g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0011g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0012g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0012g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0012g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0013g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0013g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0015g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0015g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0016g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0016g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0017g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0017g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0019g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0020g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0021g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0022g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0023g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0026g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0027g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0028g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0029g0328 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0031g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0006t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0006t0006g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0011t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0011t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0012t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0019t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0022t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0002c0002t0013g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0002c0002t0014g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0002c0002t0014g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0002c0002t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0002c0009t0024g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0002c0009t0025g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0003c0003t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0003c0003t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0003c0003t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0003c0003t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0004c0004t0009g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0004c0004t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0004c0004t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0005c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0005c0005t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0005c0005t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0006c0008t0014g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0006c0008t0030g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0007c0010t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0007c0010t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0008c0007t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0008c0007t0003g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0009c0021t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0010c0013t0006g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0011c0017t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0012c0020t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0013c0015t0018g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0014c0014t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0015c0016t0011g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0016c0018t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0294 | EUR | GBR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | GBR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0325 | EUR | GBR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0320 | EUR | FIN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0076 | EUR | FIN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00323 | hp2 | a0001 | c0001 | t0012 | g0271 | EUR | FIN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00408 | hp2 | a0001 | c0022 | t0006 | g0060 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00438 | hp2 | a0001 | c0001 | t0011 | g0268 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00544 | hp1 | a0009 | c0021 | t0001 | g0132 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00597 | hp1 | a0001 | c0001 | t0022 | g0090 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00639 | hp2 | a0001 | c0001 | t0017 | g0299 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00642 | hp2 | a0001 | c0001 | t0008 | g0289 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0279 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0287 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0045 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01074 | hp2 | a0002 | c0009 | t0024 | g0196 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0347 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01109 | hp1 | a0010 | c0013 | t0006 | g0109 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0317 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0246 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0301 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0326 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01243 | hp2 | a0001 | c0001 | t0008 | g0143 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0344 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0343 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01358 | hp1 | a0001 | c0001 | t0023 | g0312 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0327 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01433 | hp2 | a0001 | c0001 | t0016 | g0100 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0110 | EUR | IBS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0210 | EUR | IBS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0215 | EUR | IBS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0234 | EUR | IBS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01891 | hp2 | a0002 | c0009 | t0025 | g0311 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0098 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0214 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02055 | hp1 | a0006 | c0008 | t0030 | g0042 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02055 | hp2 | a0001 | c0001 | t0013 | g0334 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0267 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02148 | hp1 | a0001 | c0001 | t0017 | g0099 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | CDX | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | CDX | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CDX | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CDX | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02257 | hp1 | a0001 | c0011 | t0007 | g0324 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0198 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02280 | hp1 | a0001 | c0011 | t0007 | g0323 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0213 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0283 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02451 | hp2 | a0001 | c0006 | t0006 | g0341 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0043 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0252 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02615 | hp1 | a0001 | c0001 | t0016 | g0340 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02622 | hp2 | a0011 | c0017 | t0001 | g0138 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02698 | hp2 | a0008 | c0007 | t0003 | g0348 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02723 | hp1 | a0002 | c0002 | t0013 | g0084 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02723 | hp2 | a0007 | c0010 | t0003 | g0180 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02735 | hp1 | a0001 | c0001 | t0031 | g0175 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0313 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02738 | hp2 | a0012 | c0020 | t0001 | g0290 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0195 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02818 | hp2 | a0004 | c0004 | t0009 | g0024 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0068 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02895 | hp1 | a0004 | c0004 | t0009 | g0035 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02896 | hp1 | a0004 | c0004 | t0009 | g0013 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02922 | hp2 | a0003 | c0003 | t0003 | g0176 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02965 | hp1 | a0003 | c0003 | t0003 | g0027 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02970 | hp1 | a0001 | c0001 | t0027 | g0144 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02976 | hp1 | a0003 | c0003 | t0003 | g0177 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0248 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03098 | hp2 | a0002 | c0002 | t0014 | g0349 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03130 | hp1 | a0001 | c0001 | t0010 | g0003 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03139 | hp1 | a0013 | c0015 | t0018 | g0187 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0197 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0184 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0337 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03209 | hp2 | a0003 | c0003 | t0003 | g0022 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03225 | hp2 | a0001 | c0006 | t0001 | g0342 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03486 | hp1 | a0001 | c0001 | t0010 | g0062 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0335 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0339 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03579 | hp1 | a0006 | c0008 | t0014 | g0063 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03654 | hp1 | a0008 | c0007 | t0003 | g0303 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0345 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03834 | hp2 | a0005 | c0005 | t0002 | g0159 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03942 | hp1 | a0001 | c0012 | t0001 | g0064 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03942 | hp2 | a0005 | c0005 | t0002 | g0158 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | STU | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | STU | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0275 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG04184 | hp2 | a0005 | c0005 | t0001 | g0154 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | STU | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | YRI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | YRI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0351 | AFR | YRI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18906 | hp2 | a0001 | c0001 | t0021 | g0352 | AFR | YRI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18946 | hp1 | a0014 | c0014 | t0001 | g0052 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18966 | hp2 | a0001 | c0001 | t0015 | g0048 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18977 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18981 | hp1 | a0015 | c0016 | t0011 | g0117 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18984 | hp1 | a0001 | c0001 | t0012 | g0240 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18987 | hp1 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18989 | hp2 | a0001 | c0001 | t0020 | g0080 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18992 | hp2 | a0001 | c0001 | t0015 | g0123 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18998 | hp1 | a0016 | c0018 | t0002 | g0034 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19030 | hp1 | a0001 | c0019 | t0001 | g0174 | AFR | LWK | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | LWK | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19043 | hp2 | a0001 | c0001 | t0013 | g0336 | AFR | LWK | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19067 | hp2 | a0001 | c0001 | t0026 | g0212 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19068 | hp2 | a0001 | c0001 | t0011 | g0113 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19072 | hp1 | a0001 | c0001 | t0028 | g0227 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19074 | hp2 | a0001 | c0001 | t0011 | g0072 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19076 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19078 | hp2 | a0001 | c0001 | t0005 | g0293 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19082 | hp1 | a0001 | c0001 | t0008 | g0161 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ASW | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20129 | hp2 | a0001 | c0001 | t0010 | g0003 | AFR | ASW | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0315 | EUR | TSI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | GIH | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0310 | SAS | GIH | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02109 | hp1 | a0002 | c0002 | t0018 | g0020 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02109 | hp2 | a0002 | c0002 | t0014 | g0350 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02486 | hp2 | a0001 | c0001 | t0019 | g0189 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02559 | hp2 | a0007 | c0010 | t0005 | g0183 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03471 | hp2 | a0001 | c0001 | t0009 | g0190 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | USA | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG06807 | hp2 | a0001 | c0001 | t0010 | g0053 | AFR | USA | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | USA | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | USA | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | LWK | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA21309 | hp2 | a0001 | c0001 | t0008 | g0181 | AFR | LWK | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
homoSapiens | chm13v2 | a0001 | c0001 | t0029 | g0328 | REF | REF | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0087 | REF | REF | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:107661658 | G | T | 1 | a0005 | 3 | HG03834.hp2 HG03942.hp2 HG04184.hp2 |
missense_variant | MODERATE | c.17G>T | p.Gly6Val | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/21 | 48/4737 | 17/2343 | 6/780 | chr7 | 107661658 | |||
chr7:107683334 | A | C | 1 | a0004 | 3 | HG02818.hp2 HG02895.hp1 HG02896.hp1 |
missense_variant | MODERATE | c.898A>C | p.Ile300Leu | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 7/21 | 929/4737 | 898/2343 | 300/780 | chr7 | 107683334 | |||
chr7:107683506 | A | T | 1 | a0003 | 4 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
missense_variant | MODERATE | c.970A>T | p.Asn324Tyr | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/21 | 1001/4737 | 970/2343 | 324/780 | chr7 | 107683506 | |||
chr7:107689112 | T | C | 1 | a0010 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1061T>C | p.Phe354Ser | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/21 | 1092/4737 | 1061/2343 | 354/780 | chr7 | 107689112 | |||
chr7:107689120 | G | A | 1 | a0014 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.1069G>A | p.Ala357Thr | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/21 | 1100/4737 | 1069/2343 | 357/780 | chr7 | 107689120 | |||
chr7:107690148 | A | T | 1 | a0009 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.1174A>T | p.Asn392Tyr | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/21 | 1205/4737 | 1174/2343 | 392/780 | chr7 | 107690148 | |||
chr7:107694642 | A | T | 1 | a0012 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1363A>T | p.Ile455Phe | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/21 | 1394/4737 | 1363/2343 | 455/780 | chr7 | 107694642 | |||
chr7:107700084 | T | C | 1 | a0013 | 1 | HG03139.hp1 | missense_variant&splice_region_variant | MODERATE | c.1616T>C | p.Ile539Thr | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 15/21 | 1647/4737 | 1616/2343 | 539/780 | chr7 | 107700084 | |||
chr7:107701183 | T | C | 1 | a0008 | 2 | HG02698.hp2 HG03654.hp1 |
missense_variant | MODERATE | c.1790T>C | p.Leu597Ser | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 16/21 | 1821/4737 | 1790/2343 | 597/780 | chr7 | 107701183 | |||
chr7:107701849 | T | G | 4 | a0002 a0006 a0007 others(1): Show |
11 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
missense_variant | MODERATE | c.1826T>G | p.Val609Gly | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/21 | 1857/4737 | 1826/2343 | 609/780 | chr7 | 107701849 | |||
chr7:107701998 | G | C | 1 | a0015 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.1975G>C | p.Val659Leu | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/21 | 2006/4737 | 1975/2343 | 659/780 | chr7 | 107701998 | |||
chr7:107704355 | G | T | 1 | a0007 | 2 | HG02559.hp2 HG02723.hp2 |
missense_variant | MODERATE | c.2059G>T | p.Asp687Tyr | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/21 | 2090/4737 | 2059/2343 | 687/780 | chr7 | 107704355 | |||
chr7:107710132 | A | G | 1 | a0016 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.2168A>G | p.His723Arg | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/21 | 2199/4737 | 2168/2343 | 723/780 | chr7 | 107710132 | |||
chr7:107710154 | G | T | 1 | a0011 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.2190G>T | p.Gln730His | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/21 | 2221/4737 | 2190/2343 | 730/780 | chr7 | 107710154 | |||
chr7:107710182 | G | A | 2 | a0006 a0007 |
4 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
missense_variant | MODERATE | c.2218G>A | p.Gly740Ser | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/21 | 2249/4737 | 2218/2343 | 740/780 | chr7 | 107710182 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:107661656 | C | A | 1 | a0001c0006 | 2 | HG02451.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.15C>A | p.Gly5Gly | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/21 | 46/4737 | 15/2343 | 5/780 | chr7 | 107661656 | |||
chr7:107661716 | G | C | 1 | a0001c0012 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.75G>C | p.Pro25Pro | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/21 | 106/4737 | 75/2343 | 25/780 | chr7 | 107661716 | |||
chr7:107663356 | C | G | 1 | a0001c0022 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.225C>G | p.Leu75Leu | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/21 | 256/4737 | 225/2343 | 75/780 | chr7 | 107663356 | |||
chr7:107695983 | C | T | 1 | a0001c0011 | 2 | HG02257.hp1 HG02280.hp1 |
synonymous_variant | LOW | c.1488C>T | p.Leu496Leu | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/21 | 1519/4737 | 1488/2343 | 496/780 | chr7 | 107695983 | |||
chr7:107698111 | C | T | 1 | a0001c0019 | 1 | NA19030.hp1 | splice_region_variant&synonymous_variant | LOW | c.1614C>T | p.Asn538Asn | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/21 | 1645/4737 | 1614/2343 | 538/780 | chr7 | 107698111 | |||
chr7:107710094 | C | T | 3 | a0002c0009 a0006c0008 a0007c0010 |
6 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
synonymous_variant | LOW | c.2130C>T | p.Asp710Asp | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/21 | 2161/4737 | 2130/2343 | 710/780 | chr7 | 107710094 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:107660847 | C | T | 1 | a0001c0001t0031 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/21 | 795 | chr7 | 107660847 | ||||||
chr7:107715457 | G | A | 1 | a0001c0001t0010 | 4 | HG03130.hp1 HG03486.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 11 | chr7 | 107715457 | ||||||
chr7:107715515 | C | A | 1 | a0001c0001t0015 | 2 | NA18966.hp2 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*69C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 69 | chr7 | 107715515 | ||||||
chr7:107715796 | C | T | 1 | a0006c0008t0030 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*350C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 350 | chr7 | 107715796 | ||||||
chr7:107715822 | A | G | 2 | a0002c0002t0014 a0006c0008t0014 |
3 | HG02109.hp2 HG03098.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*376A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 376 | chr7 | 107715822 | ||||||
chr7:107716060 | C | T | 2 | a0001c0001t0011 a0015c0016t0011 |
4 | HG00438.hp2 NA18981.hp1 NA19068.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*614C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 614 | chr7 | 107716060 | ||||||
chr7:107716138 | C | A | 1 | a0001c0001t0016 | 2 | HG01433.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*692C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 692 | chr7 | 107716138 | ||||||
chr7:107716145 | G | A | 1 | a0001c0001t0019 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*699G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 699 | chr7 | 107716145 | ||||||
chr7:107716174 | GATCAAAA others(6): Show |
G | 1 | a0001c0001t0028 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*731_*743delCAAAAA others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 731 | INFO_REALIGN_3_PRIME | chr7 | 107716174 | |||||
chr7:107716252 | A | G | 2 | a0002c0002t0018 a0013c0015t0018 |
2 | HG02109.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*806A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 806 | chr7 | 107716252 | ||||||
chr7:107716314 | G | A | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(5): Show |
99 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*868G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 868 | chr7 | 107716314 | ||||||
chr7:107716505 | T | C | 1 | a0001c0001t0017 | 2 | HG00639.hp2 HG02148.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1059T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1059 | chr7 | 107716505 | ||||||
chr7:107716535 | T | C | 1 | a0001c0001t0021 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1089T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1089 | chr7 | 107716535 | ||||||
chr7:107716748 | T | G | 3 | a0001c0001t0009 a0001c0001t0010 a0004c0004t0009 |
9 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1302T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1302 | chr7 | 107716748 | ||||||
chr7:107716890 | T | C | 1 | a0001c0001t0022 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1444T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1444 | chr7 | 107716890 | ||||||
chr7:107717056 | C | T | 1 | a0001c0001t0020 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1610C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1610 | chr7 | 107717056 | ||||||
chr7:107717128 | C | T | 1 | a0001c0001t0027 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1682C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1682 | chr7 | 107717128 | ||||||
chr7:107717235 | G | A | 1 | a0001c0001t0023 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1789G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1789 | chr7 | 107717235 | ||||||
chr7:107717243 | G | C | 7 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0016 others(4): Show |
15 | HG01433.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1797G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1797 | chr7 | 107717243 | ||||||
chr7:107717351 | G | A | 2 | a0002c0009t0024 a0002c0009t0025 |
2 | HG01074.hp2 HG01891.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1905G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1905 | chr7 | 107717351 | ||||||
chr7:107717365 | C | CA | 2 | a0001c0001t0008 a0002c0009t0024 |
8 | HG00642.hp2 HG01074.hp2 HG01243.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1944dupA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1945 | INFO_REALIGN_3_PRIME | chr7 | 107717365 | |||||
chr7:107717365 | CA | C | 2 | a0001c0001t0005 a0007c0010t0005 |
13 | HG00140.hp2 HG01069.hp1 HG01169.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1944delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1944 | INFO_REALIGN_3_PRIME | chr7 | 107717365 | |||||
chr7:107717365 | CAA | C | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0013 others(19): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*1943_*1944delAA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1943 | INFO_REALIGN_3_PRIME | chr7 | 107717365 | |||||
chr7:107717365 | CAAA | C | 13 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(10): Show |
101 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1942_*1944delAAA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1942 | INFO_REALIGN_3_PRIME | chr7 | 107717365 | |||||
chr7:107717387 | AAAAG | A | 3 | a0001c0001t0009 a0001c0001t0010 a0004c0004t0009 |
9 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1943_*1946delAAGA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1943 | INFO_REALIGN_3_PRIME | chr7 | 107717387 | |||||
chr7:107717428 | C | A | 1 | a0001c0001t0026 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1982C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1982 | chr7 | 107717428 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:107660893 | G | A | 1 | a0004c0004t0009g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-4+38G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107660893 | |||||||
chr7:107660945 | T | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+90T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107660945 | |||||||
chr7:107660963 | G | A | 1 | a0004c0004t0009g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-4+108G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107660963 | |||||||
chr7:107660984 | C | T | 1 | a0001c0001t0001g0353 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-4+129C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107660984 | |||||||
chr7:107661086 | T | C | 1 | a0001c0001t0001g0021 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-4+231T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661086 | |||||||
chr7:107661121 | C | G | 5 | a0001c0001t0005g0351 a0001c0001t0021g0352 a0002c0002t0014g0349 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+266C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661121 | |||||||
chr7:107661268 | G | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-371G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661268 | |||||||
chr7:107661378 | C | T | 2 | a0001c0001t0002g0347 a0008c0007t0003g0348 |
2 | HG01106.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-3-261C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661378 | |||||||
chr7:107661395 | C | T | 2 | a0001c0001t0001g0346 a0001c0001t0003g0345 |
2 | HG01261.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-3-244C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661395 | |||||||
chr7:107661429 | G | A | 1 | a0003c0003t0003g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-3-210G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661429 | |||||||
chr7:107661444 | C | T | 2 | a0001c0001t0003g0343 a0001c0001t0003g0344 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-3-195C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661444 | |||||||
chr7:107661615 | T | A | 1 | a0001c0001t0001g0023 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-3-24T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661615 | |||||||
chr7:107661955 | T | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0003c0003t0003g0027 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+150T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107661955 | |||||||
chr7:107662005 | G | A | 1 | a0001c0001t0003g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.164+200G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107662005 | |||||||
chr7:107662463 | C | A | 1 | a0001c0001t0001g0029 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.164+658C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107662463 | |||||||
chr7:107662489 | A | G | 2 | a0001c0006t0001g0342 a0001c0006t0006g0341 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.164+684A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107662489 | |||||||
chr7:107662670 | T | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-626T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107662670 | |||||||
chr7:107662924 | A | G | 5 | a0001c0001t0005g0351 a0001c0001t0021g0352 a0002c0002t0014g0349 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-372A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107662924 | |||||||
chr7:107663177 | A | T | 258 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.165-119A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107663177 | |||||||
chr7:107663183 | C | T | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.165-113C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107663183 | |||||||
chr7:107663751 | C | T | 258 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.304+316C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663751 | |||||||
chr7:107663791 | C | T | 7 | a0001c0001t0001g0338 a0001c0001t0007g0335 a0001c0001t0007g0337 others(4): Show |
7 | HG02055.hp2 HG02615.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.304+356C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663791 | |||||||
chr7:107663828 | C | A | 5 | a0001c0001t0005g0351 a0001c0001t0021g0352 a0002c0002t0014g0349 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.304+393C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663828 | |||||||
chr7:107663832 | C | T | 5 | a0001c0001t0005g0351 a0001c0001t0021g0352 a0002c0002t0014g0349 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.304+397C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663832 | |||||||
chr7:107663926 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.304+491G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663926 | |||||||
chr7:107663933 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG00642.hp1 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.304+498T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663933 | |||||||
chr7:107663943 | A | C | 1 | a0001c0001t0002g0333 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.304+508A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663943 | |||||||
chr7:107663992 | A | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG00642.hp1 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.304+557A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663992 | |||||||
chr7:107664183 | C | T | 149 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(146): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.304+748C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664183 | |||||||
chr7:107664255 | A | G | 1 | a0001c0019t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.304+820A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664255 | |||||||
chr7:107664265 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.304+830T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664265 | |||||||
chr7:107664388 | T | A | 12 | a0001c0001t0001g0023 a0001c0001t0001g0125 a0001c0001t0001g0126 others(9): Show |
12 | HG00544.hp1 HG00621.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.304+953T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664388 | |||||||
chr7:107664395 | C | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.304+960C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664395 | |||||||
chr7:107664422 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.304+987G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664422 | |||||||
chr7:107664429 | G | A | 1 | a0001c0001t0003g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.304+994G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664429 | |||||||
chr7:107664521 | C | T | 1 | a0004c0004t0009g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.304+1086C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664521 | |||||||
chr7:107664670 | G | A | 128 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
131 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.304+1235G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664670 | |||||||
chr7:107664807 | C | G | 15 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(12): Show |
15 | HG00544.hp1 HG00621.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.304+1372C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664807 | |||||||
chr7:107664815 | C | G | 1 | a0001c0001t0001g0332 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.304+1380C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664815 | |||||||
chr7:107664883 | A | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.304+1448A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664883 | |||||||
chr7:107664886 | G | A | 1 | a0002c0009t0025g0311 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.304+1451G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664886 | |||||||
chr7:107664968 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.304+1533C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664968 | |||||||
chr7:107664985 | A | G | 1 | a0001c0001t0008g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.304+1550A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664985 | |||||||
chr7:107665079 | C | T | 2 | a0001c0001t0002g0310 a0001c0001t0021g0352 |
2 | NA18906.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.304+1644C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665079 | |||||||
chr7:107665145 | A | G | 1 | a0001c0001t0007g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.304+1710A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665145 | |||||||
chr7:107665243 | G | A | 6 | a0001c0001t0001g0178 a0001c0001t0001g0353 a0001c0001t0003g0179 others(3): Show |
6 | HG02723.hp2 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.304+1808G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665243 | |||||||
chr7:107665599 | T | C | 1 | a0001c0001t0021g0352 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.304+2164T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665599 | |||||||
chr7:107665657 | CA | C | 4 | a0001c0001t0001g0172 a0001c0001t0003g0171 a0001c0006t0001g0342 others(1): Show |
4 | HG00735.hp2 HG01255.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+2224delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 107665657 | ||||||
chr7:107665705 | C | T | 1 | a0001c0001t0007g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.304+2270C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665705 | |||||||
chr7:107665822 | C | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0112 others(47): Show |
51 | HG00544.hp1 HG00621.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.304+2387C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665822 | |||||||
chr7:107665976 | C | T | 44 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0016 others(41): Show |
46 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.304+2541C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665976 | |||||||
chr7:107666019 | C | T | 1 | a0004c0004t0009g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.304+2584C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666019 | |||||||
chr7:107666020 | T | C | 1 | a0004c0004t0009g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.304+2585T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666020 | |||||||
chr7:107666046 | A | C | 1 | a0007c0010t0003g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.304+2611A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666046 | |||||||
chr7:107666053 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0003c0003t0003g0027 others(1): Show |
4 | HG02559.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.304+2618G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666053 | |||||||
chr7:107666304 | C | G | 2 | a0001c0001t0008g0181 a0002c0009t0025g0311 |
2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.304+2869C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666304 | |||||||
chr7:107666379 | G | T | 23 | a0001c0001t0001g0006 a0001c0001t0001g0186 a0001c0001t0001g0188 others(20): Show |
25 | HG01074.hp2 HG02055.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.304+2944G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666379 | |||||||
chr7:107666404 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0008g0198 others(1): Show |
4 | HG02258.hp1 HG02559.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+2969T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666404 | |||||||
chr7:107666454 | T | C | 76 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0015 others(73): Show |
78 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.304+3019T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666454 | |||||||
chr7:107666465 | G | T | 1 | a0001c0001t0001g0346 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.304+3030G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666465 | |||||||
chr7:107666622 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.304+3187A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666622 | |||||||
chr7:107666676 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.304+3241A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666676 | |||||||
chr7:107666685 | A | G | 3 | a0001c0001t0001g0182 a0001c0006t0001g0342 a0001c0006t0006g0341 |
3 | HG02451.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.304+3250A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666685 | |||||||
chr7:107666761 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
88 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.304+3326C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666761 | |||||||
chr7:107666817 | T | C | 2 | a0001c0001t0004g0205 a0001c0001t0004g0206 |
2 | NA18983.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.304+3382T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666817 | |||||||
chr7:107666940 | A | G | 2 | a0001c0001t0002g0089 a0001c0001t0005g0326 |
2 | HG01175.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.304+3505A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666940 | |||||||
chr7:107667013 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.304+3578A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667013 | |||||||
chr7:107667092 | G | C | 3 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0209 |
3 | NA18940.hp1 NA18953.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.304+3657G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667092 | |||||||
chr7:107667141 | T | C | 3 | a0001c0001t0027g0144 a0001c0019t0001g0174 a0007c0010t0005g0183 |
3 | HG02559.hp2 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.304+3706T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667141 | |||||||
chr7:107667316 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.304+3881G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667316 | |||||||
chr7:107667458 | GT | G | 49 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0085 others(46): Show |
51 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.304+4026delT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 107667458 | ||||||
chr7:107667460 | T | TA | 14 | a0001c0001t0001g0018 a0001c0001t0002g0032 a0001c0001t0002g0033 others(11): Show |
14 | HG00099.hp1 HG00741.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.304+4025_304+4026i others(3): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667460 | |||||||
chr7:107667460 | T | TAA | 72 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0017 others(69): Show |
75 | HG00408.hp2 HG00544.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.304+4025_304+4026i others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667460 | |||||||
chr7:107667460 | T | TAAA | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.304+4025_304+4026i others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667460 | |||||||
chr7:107667460 | T | TAAAA | 19 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(16): Show |
19 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.304+4025_304+4026i others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667460 | |||||||
chr7:107667460 | TTAAAAAA others(4): Show |
T | 1 | a0001c0001t0002g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.304+4026_304+4036d others(13): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667460 | |||||||
chr7:107667461 | T | A | 303 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(300): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.304+4026T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667461 | |||||||
chr7:107667487 | C | T | 1 | a0003c0003t0003g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.304+4052C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667487 | |||||||
chr7:107667733 | G | A | 1 | a0001c0001t0007g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.304+4298G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667733 | |||||||
chr7:107667896 | C | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(225): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.305-4242C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667896 | |||||||
chr7:107667934 | A | C | 2 | a0001c0001t0003g0179 a0003c0003t0003g0022 |
2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.305-4204A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667934 | |||||||
chr7:107668131 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.305-4007C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668131 | |||||||
chr7:107668532 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.305-3606G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668532 | |||||||
chr7:107668611 | A | G | 3 | a0002c0002t0013g0084 a0002c0002t0014g0349 a0002c0002t0014g0350 |
3 | HG02109.hp2 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.305-3527A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668611 | |||||||
chr7:107668713 | G | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0071 others(17): Show |
21 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.305-3425G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668713 | |||||||
chr7:107668803 | C | T | 1 | a0012c0020t0001g0290 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.305-3335C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668803 | |||||||
chr7:107668804 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0071 others(2): Show |
6 | HG03225.hp2 HG03471.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.305-3334G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668804 | |||||||
chr7:107668992 | T | C | 11 | a0001c0001t0007g0197 a0001c0001t0016g0340 a0001c0011t0007g0323 others(8): Show |
11 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.305-3146T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668992 | |||||||
chr7:107669159 | T | C | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.305-2979T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669159 | |||||||
chr7:107669167 | G | A | 6 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0006g0045 others(3): Show |
6 | HG00408.hp2 HG01074.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.305-2971G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669167 | |||||||
chr7:107669217 | G | A | 1 | a0002c0009t0025g0311 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.305-2921G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669217 | |||||||
chr7:107669299 | C | T | 4 | a0001c0019t0001g0174 a0002c0009t0024g0196 a0002c0009t0025g0311 others(1): Show |
4 | HG01074.hp2 HG01891.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-2839C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669299 | |||||||
chr7:107669302 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
8 | HG02922.hp2 HG02976.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-2836G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669302 | |||||||
chr7:107669353 | A | G | 5 | a0001c0001t0001g0102 a0001c0001t0001g0142 a0001c0001t0001g0182 others(2): Show |
5 | HG02258.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-2785A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669353 | |||||||
chr7:107669367 | G | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(226): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.305-2771G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669367 | |||||||
chr7:107669419 | C | T | 4 | a0001c0001t0002g0280 a0001c0001t0002g0333 a0001c0001t0003g0281 others(1): Show |
4 | NA18977.hp2 NA19011.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.305-2719C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669419 | |||||||
chr7:107669690 | T | C | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.305-2448T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669690 | |||||||
chr7:107669802 | T | C | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.305-2336T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669802 | |||||||
chr7:107670018 | A | C | 2 | a0001c0001t0001g0233 a0001c0001t0001g0242 |
2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.305-2120A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670018 | |||||||
chr7:107670082 | T | C | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.305-2056T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670082 | |||||||
chr7:107670112 | A | AT | 216 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(213): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.305-2011dupT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 107670112 | ||||||
chr7:107670112 | AT | A | 9 | a0001c0001t0005g0246 a0001c0001t0016g0340 a0001c0019t0001g0174 others(6): Show |
9 | HG01074.hp2 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.305-2011delT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 107670112 | ||||||
chr7:107670177 | T | A | 1 | a0001c0001t0001g0014 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.305-1961T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670177 | |||||||
chr7:107670411 | C | T | 4 | a0001c0019t0001g0174 a0002c0009t0024g0196 a0002c0009t0025g0311 others(1): Show |
4 | HG01074.hp2 HG01891.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-1727C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670411 | |||||||
chr7:107670427 | G | A | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.305-1711G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670427 | |||||||
chr7:107670743 | A | G | 2 | a0001c0001t0003g0288 a0001c0001t0005g0279 |
2 | HG01069.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.305-1395A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670743 | |||||||
chr7:107670847 | ATG | A | 3 | a0002c0002t0014g0349 a0002c0002t0014g0350 a0003c0003t0003g0027 |
3 | HG02109.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.305-1289_305-1288d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 107670847 | ||||||
chr7:107670957 | A | G | 3 | a0001c0001t0007g0184 a0004c0004t0009g0013 a0004c0004t0009g0024 |
3 | HG02818.hp2 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.305-1181A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670957 | |||||||
chr7:107670973 | GTTGTC | G | 3 | a0001c0001t0001g0088 a0001c0001t0008g0198 a0013c0015t0018g0187 |
3 | HG02258.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.305-1158_305-1154d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 107670973 | ||||||
chr7:107671085 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.305-1053C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671085 | |||||||
chr7:107671102 | C | A | 1 | a0003c0003t0003g0027 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.305-1036C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671102 | |||||||
chr7:107671265 | C | T | 1 | a0001c0001t0002g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.305-873C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671265 | |||||||
chr7:107671308 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.305-830G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671308 | |||||||
chr7:107671345 | A | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0231 a0001c0001t0001g0232 others(4): Show |
7 | HG01069.hp2 HG01261.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.305-793A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671345 | |||||||
chr7:107671375 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0003g0046 a0001c0001t0003g0093 others(1): Show |
4 | HG00280.hp1 HG01109.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-763G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671375 | |||||||
chr7:107671396 | C | G | 7 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.305-742C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671396 | |||||||
chr7:107671495 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.305-643T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671495 | |||||||
chr7:107671594 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.305-544T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671594 | |||||||
chr7:107671632 | T | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(186): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.305-506T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671632 | |||||||
chr7:107671660 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.305-478G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671660 | |||||||
chr7:107671681 | A | C | 1 | a0001c0001t0003g0287 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.305-457A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671681 | |||||||
chr7:107671751 | G | A | 3 | a0001c0001t0003g0248 a0008c0007t0003g0303 a0008c0007t0003g0348 |
3 | HG02698.hp2 HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.305-387G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671751 | |||||||
chr7:107671904 | C | T | 1 | a0007c0010t0003g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.305-234C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671904 | |||||||
chr7:107672323 | T | C | 1 | a0001c0001t0007g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.415+75T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107672323 | |||||||
chr7:107672433 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.415+185G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107672433 | |||||||
chr7:107672488 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.415+240T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107672488 | |||||||
chr7:107672668 | A | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0071 others(7): Show |
11 | HG02818.hp2 HG02896.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.415+420A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107672668 | |||||||
chr7:107672879 | C | T | 4 | a0001c0001t0001g0139 a0001c0001t0003g0134 a0001c0001t0003g0137 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+631C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107672879 | |||||||
chr7:107673268 | C | T | 1 | a0007c0010t0003g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.416-896C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673268 | |||||||
chr7:107673282 | A | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
8 | HG02922.hp2 HG02976.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-882A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673282 | |||||||
chr7:107673407 | A | G | 6 | a0001c0001t0001g0125 a0001c0001t0002g0245 a0001c0001t0002g0277 others(3): Show |
6 | HG02015.hp1 HG02135.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-757A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673407 | |||||||
chr7:107673481 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.416-683T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673481 | |||||||
chr7:107673502 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(185): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.416-662G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673502 | |||||||
chr7:107673709 | C | T | 1 | a0001c0001t0003g0287 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.416-455C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673709 | |||||||
chr7:107673968 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
8 | HG02922.hp2 HG02976.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-196C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673968 | |||||||
chr7:107674041 | C | A | 2 | a0001c0011t0007g0323 a0001c0011t0007g0324 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.416-123C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107674041 | |||||||
chr7:107674148 | G | T | 4 | a0001c0001t0016g0340 a0002c0002t0014g0349 a0002c0002t0014g0350 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-16G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107674148 | |||||||
chr7:107674151 | T | C | 3 | a0001c0001t0003g0005 a0001c0001t0009g0190 a0001c0001t0019g0189 |
4 | HG02486.hp2 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-13T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107674151 | |||||||
chr7:107674157 | T | C | 1 | a0001c0001t0008g0198 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.416-7T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107674157 | |||||||
chr7:107674431 | C | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.600+83C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 5/20 | chr7 | 107674431 | |||||||
chr7:107674484 | G | A | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.600+136G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 5/20 | chr7 | 107674484 | |||||||
chr7:107674651 | G | A | 1 | a0001c0001t0003g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.601-294G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 5/20 | chr7 | 107674651 | |||||||
chr7:107674679 | T | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(232): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.601-266T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 5/20 | chr7 | 107674679 | |||||||
chr7:107675191 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.765+82C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675191 | |||||||
chr7:107675285 | T | TA | 6 | a0001c0001t0001g0147 a0001c0001t0001g0156 a0001c0001t0002g0170 others(3): Show |
6 | HG02027.hp1 HG02922.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.765+197dupA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675285 | ||||||
chr7:107675285 | TA | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.765+197delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675285 | ||||||
chr7:107675285 | TAA | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0353 a0001c0019t0001g0174 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+196_765+197del others(2): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675285 | ||||||
chr7:107675301 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.765+192A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675301 | |||||||
chr7:107675303 | A | AAAG | 8 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(5): Show |
8 | HG00741.hp2 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.765+196_765+197ins others(3): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675303 | ||||||
chr7:107675303 | A | G | 23 | a0001c0001t0001g0021 a0001c0001t0001g0086 a0001c0001t0001g0139 others(20): Show |
23 | HG00642.hp2 HG01074.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.765+194A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675303 | |||||||
chr7:107675358 | T | C | 1 | a0001c0001t0007g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.765+249T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675358 | |||||||
chr7:107675426 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.765+317G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675426 | |||||||
chr7:107675462 | G | A | 3 | a0001c0019t0001g0174 a0002c0009t0024g0196 a0002c0009t0025g0311 |
3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.765+353G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675462 | |||||||
chr7:107675500 | C | T | 1 | a0001c0001t0004g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.765+391C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675500 | |||||||
chr7:107675574 | C | CT | 20 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(17): Show |
20 | HG01433.hp1 HG01433.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.765+482dupT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675574 | ||||||
chr7:107675574 | CT | C | 9 | a0001c0001t0001g0115 a0001c0001t0001g0156 a0001c0001t0002g0318 others(6): Show |
9 | HG01891.hp2 HG02922.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.765+482delT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675574 | ||||||
chr7:107675574 | CTT | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(46): Show |
52 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.765+481_765+482del others(2): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675574 | ||||||
chr7:107675575 | T | C | 1 | a0002c0009t0024g0196 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.765+466T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675575 | |||||||
chr7:107675655 | C | T | 7 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.765+546C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675655 | |||||||
chr7:107675719 | G | A | 2 | a0001c0001t0002g0074 a0001c0001t0012g0271 |
2 | HG00323.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.765+610G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675719 | |||||||
chr7:107676207 | A | G | 1 | a0001c0001t0002g0274 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.765+1098A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676207 | |||||||
chr7:107676314 | G | C | 2 | a0007c0010t0003g0180 a0007c0010t0005g0183 |
2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.765+1205G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676314 | |||||||
chr7:107676392 | G | A | 5 | a0001c0019t0001g0174 a0002c0002t0014g0349 a0002c0002t0014g0350 others(2): Show |
5 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.765+1283G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676392 | |||||||
chr7:107676418 | A | G | 1 | a0001c0001t0008g0161 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.765+1309A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676418 | |||||||
chr7:107676436 | G | A | 3 | a0001c0001t0007g0197 a0001c0011t0007g0323 a0001c0011t0007g0324 |
3 | HG02257.hp1 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.765+1327G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676436 | |||||||
chr7:107676566 | G | A | 2 | a0001c0001t0002g0280 a0001c0001t0002g0333 |
2 | NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.765+1457G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676566 | |||||||
chr7:107676650 | T | G | 16 | a0001c0001t0001g0086 a0001c0001t0001g0139 a0001c0001t0002g0103 others(13): Show |
16 | HG00558.hp1 HG00642.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.765+1541T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676650 | |||||||
chr7:107676730 | G | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.765+1621G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676730 | |||||||
chr7:107676798 | C | T | 3 | a0001c0019t0001g0174 a0002c0009t0024g0196 a0002c0009t0025g0311 |
3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.765+1689C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676798 | |||||||
chr7:107677081 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0172 a0001c0001t0005g0325 |
4 | HG00140.hp2 HG00735.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+1972G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677081 | |||||||
chr7:107677099 | C | T | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.765+1990C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677099 | |||||||
chr7:107677210 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.765+2101C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677210 | |||||||
chr7:107677247 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.765+2138C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677247 | |||||||
chr7:107677265 | A | G | 182 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.765+2156A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677265 | |||||||
chr7:107677420 | G | A | 2 | a0001c0011t0007g0323 a0001c0011t0007g0324 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.765+2311G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677420 | |||||||
chr7:107677471 | C | T | 3 | a0004c0004t0009g0013 a0004c0004t0009g0024 a0004c0004t0009g0035 |
3 | HG02818.hp2 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.765+2362C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677471 | |||||||
chr7:107677608 | A | AT | 8 | a0001c0001t0001g0204 a0001c0001t0001g0222 a0001c0001t0002g0118 others(5): Show |
8 | HG01074.hp2 HG01928.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.765+2514dupT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107677608 | ||||||
chr7:107677608 | AT | A | 11 | a0001c0001t0001g0075 a0001c0001t0001g0229 a0001c0001t0002g0207 others(8): Show |
11 | HG01069.hp1 HG01169.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.765+2514delT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107677608 | ||||||
chr7:107677671 | T | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0065 a0001c0001t0001g0097 others(10): Show |
14 | HG00408.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.765+2562T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677671 | |||||||
chr7:107677792 | A | G | 2 | a0007c0010t0003g0180 a0007c0010t0005g0183 |
2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.765+2683A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677792 | |||||||
chr7:107677853 | G | A | 3 | a0001c0001t0002g0076 a0001c0001t0002g0215 a0001c0001t0002g0234 |
3 | HG00323.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.765+2744G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677853 | |||||||
chr7:107677970 | G | T | 174 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.765+2861G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677970 | |||||||
chr7:107678002 | C | G | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.765+2893C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107678002 | |||||||
chr7:107678342 | C | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0129 others(5): Show |
8 | HG00544.hp1 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.765+3233C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107678342 | |||||||
chr7:107678598 | C | T | 5 | a0001c0019t0001g0174 a0002c0002t0014g0349 a0002c0002t0014g0350 others(2): Show |
5 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.765+3489C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107678598 | |||||||
chr7:107678633 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.765+3524A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107678633 | |||||||
chr7:107678737 | G | GA | 12 | a0001c0001t0001g0102 a0001c0001t0001g0135 a0001c0001t0001g0140 others(9): Show |
12 | HG01891.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.765+3642dupA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107678737 | ||||||
chr7:107678737 | GA | G | 145 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(142): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.765+3642delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107678737 | ||||||
chr7:107678737 | GAA | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(47): Show |
53 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.765+3641_765+3642d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107678737 | ||||||
chr7:107678840 | T | A | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.765+3731T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107678840 | |||||||
chr7:107679047 | A | G | 1 | a0001c0001t0004g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.765+3938A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679047 | |||||||
chr7:107679526 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.766-3676G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679526 | |||||||
chr7:107679709 | C | CTTTATAT others(34): Show |
2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.766-3492_766-3491i others(43): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679709 | ||||||
chr7:107679711 | A | G | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.766-3491A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679711 | |||||||
chr7:107679781 | A | G | 1 | a0001c0001t0005g0326 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.766-3421A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679781 | |||||||
chr7:107679796 | A | AAATATAA others(16): Show |
1 | a0001c0001t0003g0171 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.766-3379_766-3357d others(25): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679796 | ||||||
chr7:107679800 | A | G | 1 | a0013c0015t0018g0187 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.766-3402A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679800 | |||||||
chr7:107679834 | T | TTATTATA others(31): Show |
1 | a0001c0001t0002g0304 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.766-3351_766-3314d others(40): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679834 | ||||||
chr7:107679858 | T | C | 4 | a0001c0001t0001g0139 a0001c0001t0003g0134 a0001c0001t0003g0137 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-3344T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679858 | |||||||
chr7:107679859 | A | C | 2 | a0001c0011t0007g0323 a0001c0011t0007g0324 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.766-3343A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679859 | |||||||
chr7:107679861 | T | A | 6 | a0001c0001t0002g0128 a0001c0001t0007g0184 a0002c0002t0013g0084 others(3): Show |
6 | HG02723.hp1 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-3341T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679861 | |||||||
chr7:107679869 | C | CTTA | 180 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.766-3331_766-3329d others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679869 | ||||||
chr7:107679869 | C | CTTATATT others(119): Show |
2 | a0004c0004t0009g0013 a0004c0004t0009g0024 |
2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.766-3324_766-3323i others(128): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679869 | ||||||
chr7:107679869 | C | CTTATATT others(78): Show |
2 | a0001c0001t0007g0184 a0004c0004t0009g0035 |
2 | HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.766-3324_766-3323i others(87): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679869 | ||||||
chr7:107679869 | C | CTTATATT others(37): Show |
2 | a0001c0001t0002g0128 a0002c0002t0013g0084 |
2 | HG02723.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.766-3324_766-3323i others(46): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679869 | ||||||
chr7:107679869 | C | CTTATTAT others(14): Show |
51 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(48): Show |
54 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.766-3329_766-3328i others(23): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679869 | ||||||
chr7:107679881 | A | G | 2 | a0001c0011t0007g0323 a0001c0011t0007g0324 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.766-3321A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679881 | |||||||
chr7:107679882 | A | C | 2 | a0001c0011t0007g0323 a0001c0011t0007g0324 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.766-3320A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679882 | |||||||
chr7:107679891 | T | A | 1 | a0001c0019t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766-3311T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679891 | |||||||
chr7:107679894 | A | C | 1 | a0001c0019t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766-3308A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679894 | |||||||
chr7:107679896 | A | T | 1 | a0001c0019t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766-3306A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679896 | |||||||
chr7:107679899 | C | A | 1 | a0001c0019t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766-3303C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679899 | |||||||
chr7:107679902 | A | ATAT | 185 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(182): Show |
192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.766-3296_766-3294d others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679902 | ||||||
chr7:107679911 | G | T | 5 | a0001c0001t0007g0184 a0002c0002t0013g0084 a0004c0004t0009g0013 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3291G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679911 | |||||||
chr7:107679944 | T | TATCTTAT others(26): Show |
1 | a0001c0001t0012g0271 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.766-3250_766-3218d others(35): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679944 | ||||||
chr7:107679947 | CTTATATA others(11): Show |
C | 7 | a0001c0011t0007g0323 a0001c0011t0007g0324 a0001c0019t0001g0174 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.766-3217_766-3200d others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679947 | ||||||
chr7:107679949 | T | C | 1 | a0001c0001t0007g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.766-3253T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679949 | |||||||
chr7:107679959 | A | AATCTTAT others(16): Show |
7 | a0001c0001t0005g0326 a0001c0001t0006g0210 a0001c0001t0007g0184 others(4): Show |
7 | HG01175.hp2 HG01358.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.766-3240_766-3218d others(25): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679959 | ||||||
chr7:107679995 | AATCTT | A | 3 | a0001c0001t0001g0131 a0001c0001t0003g0171 a0009c0021t0001g0132 |
3 | HG00544.hp1 HG01255.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.766-3199_766-3195d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679995 | ||||||
chr7:107680015 | T | C | 3 | a0001c0001t0003g0248 a0008c0007t0003g0303 a0008c0007t0003g0348 |
3 | HG02698.hp2 HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.766-3187T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680015 | |||||||
chr7:107680021 | CTTA | C | 9 | a0001c0001t0001g0075 a0001c0001t0001g0085 a0001c0001t0001g0247 others(6): Show |
9 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.766-3176_766-3174d others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680021 | ||||||
chr7:107680022 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.766-3180T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680022 | |||||||
chr7:107680059 | AATCTTAT others(16): Show |
A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3127_766-3105d others(25): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680059 | ||||||
chr7:107680063 | TTATTA | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3135_766-3131d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680063 | ||||||
chr7:107680063 | TTATTATA others(108): Show |
T | 3 | a0003c0003t0003g0027 a0003c0003t0003g0176 a0003c0003t0003g0177 |
3 | HG02922.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.766-3135_766-3021d others(2): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680063 | ||||||
chr7:107680078 | T | A | 9 | a0001c0001t0001g0071 a0001c0001t0001g0135 a0001c0001t0001g0140 others(6): Show |
9 | HG01255.hp1 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.766-3124T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680078 | |||||||
chr7:107680084 | T | A | 5 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3118T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680084 | |||||||
chr7:107680085 | C | T | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.766-3117C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680085 | |||||||
chr7:107680090 | T | A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3112T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680090 | |||||||
chr7:107680090 | T | TATATAAT others(39): Show |
5 | a0001c0001t0001g0031 a0001c0001t0001g0188 a0001c0001t0001g0194 others(2): Show |
5 | HG00438.hp2 HG02155.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.766-3030_766-2985d others(48): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680090 | ||||||
chr7:107680090 | TATATAAT others(16): Show |
T | 137 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(134): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.766-3007_766-2985d others(25): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680090 | ||||||
chr7:107680090 | TATATAAT others(39): Show |
T | 1 | a0001c0001t0004g0205 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.766-3030_766-2985d others(48): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680090 | ||||||
chr7:107680098 | C | A | 9 | a0001c0001t0001g0071 a0001c0001t0001g0135 a0001c0001t0001g0140 others(6): Show |
9 | HG01255.hp1 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.766-3104C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680098 | |||||||
chr7:107680100 | T | A | 9 | a0001c0001t0001g0071 a0001c0001t0001g0135 a0001c0001t0001g0140 others(6): Show |
9 | HG01255.hp1 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.766-3102T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680100 | |||||||
chr7:107680102 | T | A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3100T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680102 | |||||||
chr7:107680108 | TATATA | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3086_766-3082d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680108 | ||||||
chr7:107680113 | A | AATATATT others(11): Show |
2 | a0001c0001t0001g0071 a0001c0001t0003g0171 |
2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.766-3084_766-3083i others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680113 | ||||||
chr7:107680119 | A | T | 2 | a0001c0001t0001g0163 a0001c0001t0009g0068 |
2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-3083A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680119 | |||||||
chr7:107680122 | TTATCTTA others(3): Show |
T | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3076_766-3067d others(12): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680122 | ||||||
chr7:107680132 | A | G | 9 | a0001c0001t0001g0075 a0001c0001t0001g0085 a0001c0001t0001g0247 others(6): Show |
9 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.766-3070A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680132 | |||||||
chr7:107680136 | A | T | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3066A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680136 | |||||||
chr7:107680141 | AATCTTAT others(21): Show |
A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG00642.hp1 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.766-3053_766-3026d others(30): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680141 | ||||||
chr7:107680149 | C | A | 5 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3053C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680149 | |||||||
chr7:107680149 | CTTATTAT others(19): Show |
C | 1 | a0001c0001t0001g0172 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.766-3048_766-3023d others(28): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680149 | ||||||
chr7:107680154 | TATATA | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3040_766-3036d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680154 | ||||||
chr7:107680164 | A | G | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.766-3038A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680164 | |||||||
chr7:107680165 | A | G | 1 | a0001c0001t0003g0294 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.766-3037A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680165 | |||||||
chr7:107680168 | TTATCTTA others(3): Show |
T | 5 | a0001c0019t0001g0174 a0002c0002t0014g0349 a0002c0002t0014g0350 others(2): Show |
5 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.766-3030_766-3021d others(12): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680168 | ||||||
chr7:107680172 | C | A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3030C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680172 | |||||||
chr7:107680177 | T | A | 5 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3025T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680177 | |||||||
chr7:107680178 | A | ATATAATA others(6): Show |
1 | a0001c0001t0001g0332 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.766-3020_766-3008d others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680178 | ||||||
chr7:107680178 | A | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3024A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680178 | |||||||
chr7:107680182 | A | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3020A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680182 | |||||||
chr7:107680185 | A | C | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3017A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680185 | |||||||
chr7:107680187 | A | T | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3015A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680187 | |||||||
chr7:107680194 | T | A | 8 | a0001c0019t0001g0174 a0002c0002t0014g0349 a0002c0002t0014g0350 others(5): Show |
8 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.766-3008T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680194 | |||||||
chr7:107680194 | T | TAATATAA others(6): Show |
69 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.766-3008_766-3007i others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680194 | |||||||
chr7:107680194 | T | TCTTATTA others(75): Show |
1 | a0001c0001t0003g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.766-2985_766-2984i others(84): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680194 | ||||||
chr7:107680195 | C | A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3007C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680195 | |||||||
chr7:107680201 | ATATAATA others(6): Show |
A | 1 | a0001c0001t0003g0315 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.766-2985_766-2973d others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680201 | ||||||
chr7:107680208 | A | C | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-2994A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680208 | |||||||
chr7:107680208 | A | G | 5 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-2994A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680208 | |||||||
chr7:107680210 | A | T | 7 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.766-2992A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680210 | |||||||
chr7:107680213 | C | A | 5 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-2989C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680213 | |||||||
chr7:107680218 | A | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(83): Show |
89 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.766-2984A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680218 | |||||||
chr7:107680219 | A | G | 1 | a0001c0001t0002g0104 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.766-2983A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680219 | |||||||
chr7:107680226 | C | A | 2 | a0001c0001t0001g0163 a0001c0001t0009g0068 |
2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2976C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680226 | |||||||
chr7:107680226 | C | G | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-2976C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680226 | |||||||
chr7:107680228 | T | A | 2 | a0001c0001t0001g0163 a0001c0001t0009g0068 |
2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2974T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680228 | |||||||
chr7:107680230 | A | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(83): Show |
89 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.766-2972A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680230 | |||||||
chr7:107680231 | C | A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-2971C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680231 | |||||||
chr7:107680236 | T | A | 2 | a0001c0001t0001g0163 a0001c0001t0009g0068 |
2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2966T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680236 | |||||||
chr7:107680236 | TATATAAT others(57): Show |
T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-2958_766-2895d others(66): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680236 | ||||||
chr7:107680244 | A | C | 4 | a0001c0001t0001g0163 a0001c0001t0003g0101 a0001c0001t0003g0179 others(1): Show |
4 | HG02886.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2958A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680244 | |||||||
chr7:107680244 | A | T | 1 | a0001c0001t0002g0278 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.766-2958A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680244 | |||||||
chr7:107680246 | A | T | 4 | a0001c0001t0001g0163 a0001c0001t0003g0101 a0001c0001t0003g0179 others(1): Show |
4 | HG02886.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2956A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680246 | |||||||
chr7:107680246 | AATCTTAT others(11): Show |
A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0224 a0001c0001t0002g0055 others(3): Show |
6 | HG01496.hp1 HG01952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-2940_766-2923d others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680246 | ||||||
chr7:107680248 | T | A | 2 | a0001c0001t0001g0163 a0001c0001t0009g0068 |
2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2954T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680248 | |||||||
chr7:107680249 | C | CTTATA | 77 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(74): Show |
80 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.766-2949_766-2948i others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680249 | ||||||
chr7:107680249 | CTTATTAT others(93): Show |
C | 2 | a0001c0001t0016g0100 a0001c0001t0016g0340 |
2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.766-2922_766-2823d others(102): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680249 | ||||||
chr7:107680262 | C | A | 2 | a0001c0001t0001g0163 a0001c0001t0009g0068 |
2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2940C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680262 | |||||||
chr7:107680262 | C | G | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-2940C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680262 | |||||||
chr7:107680264 | T | A | 2 | a0001c0001t0001g0163 a0001c0001t0009g0068 |
2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2938T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680264 | |||||||
chr7:107680267 | C | A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0179 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-2935C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680267 | |||||||
chr7:107680272 | T | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(74): Show |
80 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.766-2930T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680272 | |||||||
chr7:107680272 | TATATA | T | 4 | a0001c0001t0001g0163 a0001c0001t0003g0101 a0001c0001t0003g0179 others(1): Show |
4 | HG02886.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2922_766-2918d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680272 | ||||||
chr7:107680273 | A | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(74): Show |
80 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.766-2929A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680273 | |||||||
chr7:107680277 | A | AATATAAT others(29): Show |
4 | a0001c0001t0001g0031 a0001c0001t0001g0188 a0001c0001t0001g0194 others(1): Show |
4 | HG02615.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2913_766-2912i others(38): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680277 | ||||||
chr7:107680277 | A | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(74): Show |
80 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.766-2925A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680277 | |||||||
chr7:107680277 | AATATAAT others(34): Show |
A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | NA18941.hp1 NA18946.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2899_766-2859d others(43): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680277 | ||||||
chr7:107680287 | T | TATTATAT others(6): Show |
6 | a0001c0001t0001g0008 a0001c0001t0001g0224 a0001c0001t0002g0055 others(3): Show |
6 | HG01496.hp1 HG01952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-2913_766-2912i others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680287 | ||||||
chr7:107680290 | C | A | 137 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(134): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.766-2912C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680290 | |||||||
chr7:107680295 | T | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0224 a0001c0001t0002g0055 others(3): Show |
6 | HG01496.hp1 HG01952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-2907T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680295 | |||||||
chr7:107680295 | TATATA | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(192): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.766-2899_766-2895d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680295 | ||||||
chr7:107680296 | A | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0224 a0001c0001t0002g0055 others(3): Show |
6 | HG01496.hp1 HG01952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-2906A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680296 | |||||||
chr7:107680300 | A | AATATAAT others(11): Show |
2 | a0001c0001t0001g0163 a0001c0001t0009g0068 |
2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2889_766-2872d others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | ||||||
chr7:107680300 | A | AATCTTAT others(6): Show |
1 | a0006c0008t0030g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766-2900_766-2899i others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | ||||||
chr7:107680300 | A | AATCTTAT others(24): Show |
4 | a0001c0001t0003g0005 a0001c0001t0003g0191 a0001c0001t0009g0190 others(1): Show |
5 | HG02486.hp2 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-2900_766-2899i others(33): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | ||||||
chr7:107680300 | A | AATCTTAT others(29): Show |
4 | a0001c0001t0007g0184 a0004c0004t0009g0013 a0004c0004t0009g0024 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-2900_766-2899i others(38): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | ||||||
chr7:107680300 | A | AATCTTAT others(65): Show |
1 | a0001c0001t0003g0171 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.766-2900_766-2899i others(74): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | ||||||
chr7:107680300 | A | AATGTTAT others(21): Show |
1 | a0001c0001t0001g0086 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.766-2900_766-2899i others(30): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | ||||||
chr7:107680300 | A | AATGTTAT others(24): Show |
13 | a0001c0001t0001g0139 a0001c0001t0003g0037 a0001c0001t0003g0134 others(10): Show |
13 | HG00642.hp2 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.766-2900_766-2899i others(33): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | ||||||
chr7:107680300 | A | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0224 a0001c0001t0002g0055 others(3): Show |
6 | HG01496.hp1 HG01952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-2902A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680300 | |||||||
chr7:107680303 | A | C | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766-2899A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680303 | |||||||
chr7:107680305 | A | T | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766-2897A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680305 | |||||||
chr7:107680308 | C | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(94): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.766-2894C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680308 | |||||||
chr7:107680313 | A | C | 1 | a0006c0008t0030g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766-2889A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680313 | |||||||
chr7:107680313 | A | T | 1 | a0001c0001t0031g0175 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.766-2889A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680313 | |||||||
chr7:107680326 | C | G | 1 | a0006c0008t0030g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766-2876C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680326 | |||||||
chr7:107680328 | T | TATATTAT others(6): Show |
1 | a0006c0008t0030g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766-2872_766-2871i others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680328 | ||||||
chr7:107680330 | T | G | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766-2872T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680330 | |||||||
chr7:107680331 | C | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | NA18941.hp1 NA18946.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2871C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680331 | |||||||
chr7:107680344 | G | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | NA18941.hp1 NA18946.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2858G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680344 | |||||||
chr7:107680361 | T | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(50): Show |
56 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.766-2841T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680361 | |||||||
chr7:107680380 | G | C | 1 | a0001c0001t0007g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.766-2822G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680380 | |||||||
chr7:107680380 | G | GTTATATT others(29): Show |
1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766-2805_766-2770d others(38): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680380 | ||||||
chr7:107680419 | A | G | 1 | a0001c0001t0006g0267 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.766-2783A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680419 | |||||||
chr7:107680489 | A | G | 1 | a0001c0001t0002g0081 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.766-2713A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680489 | |||||||
chr7:107680666 | G | A | 14 | a0001c0001t0001g0086 a0001c0001t0001g0139 a0001c0001t0003g0037 others(11): Show |
14 | HG00642.hp2 HG01243.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.766-2536G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680666 | |||||||
chr7:107680757 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(236): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.766-2445G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680757 | |||||||
chr7:107681081 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.766-2121T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681081 | |||||||
chr7:107681129 | A | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(265): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.766-2073A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681129 | |||||||
chr7:107681130 | A | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(265): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.766-2072A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681130 | |||||||
chr7:107681221 | T | A | 55 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(52): Show |
57 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.766-1981T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681221 | |||||||
chr7:107681270 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.766-1932A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681270 | |||||||
chr7:107681313 | C | T | 12 | a0001c0001t0001g0338 a0001c0001t0007g0335 a0001c0001t0007g0337 others(9): Show |
12 | HG01074.hp2 HG01433.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.766-1889C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681313 | |||||||
chr7:107681316 | T | C | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766-1886T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681316 | |||||||
chr7:107681567 | TAAAGA | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(56): Show |
62 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.766-1630_766-1626d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107681567 | ||||||
chr7:107681674 | G | C | 34 | a0001c0001t0001g0139 a0001c0001t0003g0028 a0001c0001t0003g0037 others(31): Show |
34 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.766-1528G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681674 | |||||||
chr7:107681703 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.766-1499A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681703 | |||||||
chr7:107681746 | C | T | 1 | a0016c0018t0002g0034 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.766-1456C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681746 | |||||||
chr7:107681779 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0330 others(1): Show |
4 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-1423T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681779 | |||||||
chr7:107681849 | T | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(7): Show |
10 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.766-1353T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681849 | |||||||
chr7:107681999 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.766-1203A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681999 | |||||||
chr7:107682021 | C | G | 1 | a0009c0021t0001g0132 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.766-1181C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682021 | |||||||
chr7:107682104 | T | TA | 37 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0070 others(34): Show |
37 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.766-1072dupA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107682104 | ||||||
chr7:107682104 | TA | T | 8 | a0001c0001t0002g0160 a0001c0001t0003g0137 a0001c0001t0003g0191 others(5): Show |
8 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.766-1072delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107682104 | ||||||
chr7:107682105 | A | T | 1 | a0001c0001t0005g0351 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.766-1097A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682105 | |||||||
chr7:107682130 | A | T | 3 | a0001c0001t0003g0179 a0002c0002t0014g0349 a0002c0002t0014g0350 |
3 | HG02109.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.766-1072A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682130 | |||||||
chr7:107682130 | AT | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0139 others(25): Show |
28 | HG01074.hp2 HG01243.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.766-1064delT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107682130 | ||||||
chr7:107682130 | ATT | A | 18 | a0001c0001t0001g0130 a0001c0001t0003g0239 a0001c0001t0003g0249 others(15): Show |
19 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.766-1065_766-1064d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107682130 | ||||||
chr7:107682131 | T | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(176): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.766-1071T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682131 | |||||||
chr7:107682132 | T | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.766-1070T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682132 | |||||||
chr7:107682133 | T | A | 6 | a0001c0001t0003g0294 a0001c0001t0007g0197 a0004c0004t0009g0013 others(3): Show |
6 | HG00099.hp2 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-1069T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682133 | |||||||
chr7:107682139 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.766-1063A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682139 | |||||||
chr7:107682235 | G | A | 1 | a0001c0001t0006g0267 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.766-967G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682235 | |||||||
chr7:107682247 | G | C | 1 | a0001c0012t0001g0064 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.766-955G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682247 | |||||||
chr7:107682661 | A | AAC | 3 | a0001c0001t0003g0179 a0002c0002t0014g0349 a0002c0002t0014g0350 |
3 | HG02109.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.766-525_766-524dup others(2): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107682661 | ||||||
chr7:107682699 | A | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0040 others(8): Show |
13 | HG00621.hp1 NA18940.hp2 NA18966.hp2 others(10): Show |
intron_variant | MODIFIER | c.766-503A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682699 | |||||||
chr7:107682744 | C | A | 4 | a0003c0003t0003g0022 a0003c0003t0003g0027 a0003c0003t0003g0176 others(1): Show |
4 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-458C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682744 | |||||||
chr7:107682746 | T | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(220): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.766-456T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682746 | |||||||
chr7:107682764 | C | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(232): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.766-438C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682764 | |||||||
chr7:107682804 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.766-398C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682804 | |||||||
chr7:107682830 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.766-372G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682830 | |||||||
chr7:107682847 | A | G | 1 | a0001c0001t0001g0329 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.766-355A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682847 | |||||||
chr7:107682989 | T | C | 1 | a0001c0001t0002g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.766-213T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682989 | |||||||
chr7:107683154 | G | A | 3 | a0001c0019t0001g0174 a0002c0009t0024g0196 a0002c0009t0025g0311 |
3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.766-48G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107683154 | |||||||
chr7:107683668 | G | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(232): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1001+131G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107683668 | |||||||
chr7:107683705 | A | G | 3 | a0001c0019t0001g0174 a0002c0009t0024g0196 a0002c0009t0025g0311 |
3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1001+168A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107683705 | |||||||
chr7:107683787 | G | C | 1 | a0001c0001t0003g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1001+250G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107683787 | |||||||
chr7:107683897 | C | G | 1 | a0001c0001t0009g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1001+360C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107683897 | |||||||
chr7:107683955 | A | G | 1 | a0001c0001t0003g0239 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1001+418A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107683955 | |||||||
chr7:107684130 | G | A | 1 | a0001c0006t0006g0341 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1001+593G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684130 | |||||||
chr7:107684224 | G | A | 1 | a0001c0001t0002g0304 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1001+687G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684224 | |||||||
chr7:107684235 | G | A | 6 | a0001c0001t0003g0005 a0001c0001t0003g0137 a0001c0001t0003g0191 others(3): Show |
7 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1001+698G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684235 | |||||||
chr7:107684285 | C | T | 3 | a0001c0001t0003g0179 a0002c0002t0014g0349 a0002c0002t0014g0350 |
3 | HG02109.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1001+748C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684285 | |||||||
chr7:107684329 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(239): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1001+792G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684329 | |||||||
chr7:107684345 | G | A | 2 | a0001c0001t0015g0048 a0001c0001t0015g0123 |
2 | NA18966.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1001+808G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684345 | |||||||
chr7:107684384 | G | T | 1 | a0001c0001t0003g0294 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1001+847G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684384 | |||||||
chr7:107684397 | G | C | 8 | a0001c0001t0003g0005 a0001c0001t0003g0137 a0001c0001t0003g0191 others(5): Show |
9 | HG02055.hp1 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1001+860G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684397 | |||||||
chr7:107684520 | A | C | 1 | a0001c0001t0001g0217 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1001+983A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684520 | |||||||
chr7:107684708 | A | C | 120 | a0001c0001t0001g0075 a0001c0001t0001g0082 a0001c0001t0001g0085 others(117): Show |
122 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1001+1171A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684708 | |||||||
chr7:107684799 | A | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0302 |
2 | NA18939.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1001+1262A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684799 | |||||||
chr7:107684835 | G | A | 3 | a0001c0019t0001g0174 a0002c0009t0024g0196 a0002c0009t0025g0311 |
3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1001+1298G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684835 | |||||||
chr7:107684936 | GTTTAGGG others(6): Show |
G | 115 | a0001c0001t0001g0075 a0001c0001t0001g0082 a0001c0001t0001g0085 others(112): Show |
116 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1001+1403_1001+141 others(17): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107684936 | ||||||
chr7:107685271 | C | T | 3 | a0001c0019t0001g0174 a0002c0009t0024g0196 a0002c0009t0025g0311 |
3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1001+1734C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685271 | |||||||
chr7:107685598 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1001+2061A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685598 | |||||||
chr7:107685610 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1001+2073T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685610 | |||||||
chr7:107685692 | C | G | 111 | a0001c0001t0001g0075 a0001c0001t0001g0082 a0001c0001t0001g0085 others(108): Show |
112 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1001+2155C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685692 | |||||||
chr7:107685771 | C | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(197): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1001+2234C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685771 | |||||||
chr7:107685861 | T | A | 6 | a0001c0001t0002g0092 a0001c0001t0002g0107 a0001c0001t0002g0170 others(3): Show |
6 | HG00438.hp2 HG02155.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001+2324T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685861 | |||||||
chr7:107685946 | T | A | 2 | a0001c0011t0007g0323 a0001c0011t0007g0324 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1001+2409T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685946 | |||||||
chr7:107686053 | A | C | 1 | a0001c0001t0001g0220 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1001+2516A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686053 | |||||||
chr7:107686108 | G | GGT | 4 | a0001c0001t0001g0125 a0001c0001t0001g0300 a0001c0001t0005g0293 others(1): Show |
4 | HG03017.hp2 HG03139.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+2586_1001+258 others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686108 | ||||||
chr7:107686121 | G | T | 1 | a0001c0001t0006g0214 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1001+2584G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686121 | |||||||
chr7:107686267 | T | C | 3 | a0001c0001t0007g0184 a0001c0011t0007g0323 a0001c0011t0007g0324 |
3 | HG02257.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1001+2730T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686267 | |||||||
chr7:107686267 | T | TCCTTCCC others(20): Show |
4 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0319 others(1): Show |
4 | HG00280.hp2 HG01258.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001+2753_1002-273 others(31): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686267 | ||||||
chr7:107686267 | TCCTTCCC others(29): Show |
T | 2 | a0001c0001t0001g0216 a0001c0001t0003g0185 |
2 | HG02622.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1002-2755_1002-272 others(40): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686267 | ||||||
chr7:107686290 | T | C | 3 | a0001c0001t0007g0184 a0001c0011t0007g0323 a0001c0011t0007g0324 |
3 | HG02257.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1001+2753T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686290 | |||||||
chr7:107686290 | TCCTACCT others(11): Show |
T | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1001+2757_1002-274 others(22): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686290 | ||||||
chr7:107686294 | A | C | 3 | a0001c0001t0007g0184 a0001c0011t0007g0323 a0001c0011t0007g0324 |
3 | HG02257.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1001+2757A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686294 | |||||||
chr7:107686294 | ACCTTCCC others(2): Show |
A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1002-2736_1002-272 others(13): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686294 | ||||||
chr7:107686298 | T | G | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1002-2755T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686298 | |||||||
chr7:107686300 | C | A | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1002-2753C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686300 | |||||||
chr7:107686303 | C | CCCTTCCC others(38): Show |
2 | a0001c0001t0001g0070 a0001c0001t0007g0184 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1002-2737_1002-273 others(49): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686303 | ||||||
chr7:107686303 | C | CCCTTTCC others(74): Show |
1 | a0001c0011t0007g0323 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1002-2746_1002-274 others(85): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686303 | ||||||
chr7:107686303 | C | CCCTTTCC others(65): Show |
1 | a0001c0011t0007g0324 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1002-2746_1002-274 others(76): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686303 | ||||||
chr7:107686309 | C | CCTCCCTT others(11): Show |
1 | a0001c0006t0001g0342 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1002-2737_1002-273 others(22): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686309 | ||||||
chr7:107686317 | C | T | 2 | a0001c0001t0001g0070 a0001c0006t0001g0342 |
2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1002-2736C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686317 | |||||||
chr7:107686324 | T | C | 2 | a0001c0001t0001g0070 a0001c0006t0001g0342 |
2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1002-2729T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686324 | |||||||
chr7:107686324 | TTTCCTAC others(20): Show |
T | 3 | a0001c0001t0004g0235 a0001c0001t0004g0254 a0001c0001t0004g0305 |
3 | NA18939.hp1 NA18992.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1002-2719_1002-269 others(31): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686324 | ||||||
chr7:107686334 | G | T | 2 | a0001c0001t0001g0070 a0001c0006t0001g0342 |
2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1002-2719G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686334 | |||||||
chr7:107686336 | A | ACTCCCTT others(20): Show |
1 | a0001c0001t0003g0171 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1002-2696_1002-267 others(31): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686336 | ||||||
chr7:107686336 | A | C | 2 | a0001c0001t0001g0070 a0001c0006t0001g0342 |
2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1002-2717A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686336 | |||||||
chr7:107686344 | T | C | 2 | a0001c0011t0007g0323 a0001c0011t0007g0324 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1002-2709T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686344 | |||||||
chr7:107686390 | C | T | 1 | a0001c0001t0004g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1002-2663C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686390 | |||||||
chr7:107686393 | C | T | 1 | a0001c0001t0004g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1002-2660C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686393 | |||||||
chr7:107686394 | C | T | 1 | a0001c0001t0004g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1002-2659C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686394 | |||||||
chr7:107686398 | C | T | 1 | a0001c0001t0004g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1002-2655C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686398 | |||||||
chr7:107686399 | T | A | 1 | a0005c0005t0001g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1002-2654T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686399 | |||||||
chr7:107686400 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1002-2653C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686400 | |||||||
chr7:107686405 | T | C | 1 | a0001c0001t0004g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1002-2648T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686405 | |||||||
chr7:107686405 | T | TC | 3 | a0001c0001t0001g0065 a0001c0001t0001g0096 a0001c0001t0004g0164 |
3 | HG02027.hp1 NA19003.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1002-2648_1002-264 others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686405 | |||||||
chr7:107686405 | T | TCTTTCTT others(26): Show |
1 | a0001c0001t0001g0226 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1002-2648_1002-264 others(37): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686405 | |||||||
chr7:107686405 | T | TTCTTTCT others(7): Show |
1 | a0001c0001t0001g0125 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1002-2647_1002-264 others(18): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | T | TTCTTTCT others(15): Show |
1 | a0001c0001t0005g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1002-2647_1002-264 others(26): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | T | TTTCTTCT others(11): Show |
1 | a0001c0001t0005g0155 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1002-2646_1002-264 others(22): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | T | TTTCTTTC others(20): Show |
1 | a0001c0001t0001g0241 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1002-2646_1002-264 others(31): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | T | TTTTC | 32 | a0001c0001t0001g0085 a0001c0001t0002g0002 a0001c0001t0002g0011 others(29): Show |
34 | HG00558.hp2 HG01123.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.1002-2600_1002-259 others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | T | TTTTCTTT others(1): Show |
22 | a0001c0001t0002g0061 a0001c0001t0002g0073 a0001c0001t0002g0160 others(19): Show |
22 | HG00639.hp2 HG01070.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1002-2604_1002-259 others(12): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | T | TTTTCTTT others(5): Show |
16 | a0001c0001t0001g0247 a0001c0001t0002g0010 a0001c0001t0002g0083 others(13): Show |
16 | HG00438.hp1 HG00438.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1002-2608_1002-259 others(16): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | T | TTTTCTTT others(9): Show |
4 | a0001c0001t0002g0128 a0001c0001t0002g0273 a0001c0001t0002g0318 others(1): Show |
4 | HG02148.hp1 HG02155.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-2612_1002-259 others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | T | TTTTCTTT others(13): Show |
2 | a0001c0001t0002g0274 a0001c0001t0016g0340 |
2 | HG00544.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1002-2616_1002-259 others(24): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | T | TTTTCTTT others(36): Show |
1 | a0001c0001t0001g0150 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1002-2626_1002-262 others(47): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | T | TTTTTTCT others(15): Show |
1 | a0001c0001t0006g0043 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1002-2645_1002-264 others(26): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | TTTTC | T | 10 | a0001c0001t0002g0103 a0001c0001t0002g0157 a0001c0001t0002g0261 others(7): Show |
10 | HG00558.hp1 HG00735.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1002-2600_1002-259 others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | TTTTCTTT others(1): Show |
T | 16 | a0001c0001t0002g0199 a0001c0001t0003g0028 a0001c0001t0003g0046 others(13): Show |
16 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1002-2604_1002-259 others(12): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686405 | TTTTCTTT others(5): Show |
T | 15 | a0001c0001t0001g0139 a0001c0001t0002g0074 a0001c0001t0003g0037 others(12): Show |
15 | HG00099.hp2 HG00642.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1002-2608_1002-259 others(16): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | ||||||
chr7:107686441 | C | CTGTTCTT others(14): Show |
1 | a0001c0001t0001g0148 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1002-2611_1002-261 others(25): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | ||||||
chr7:107686441 | C | CTT | 5 | a0001c0001t0001g0125 a0001c0001t0001g0241 a0001c0001t0005g0146 others(2): Show |
5 | HG01261.hp1 HG02602.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002-2610_1002-260 others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | ||||||
chr7:107686441 | C | CTTTCTTT others(3): Show |
9 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0001g0140 others(6): Show |
10 | HG01074.hp1 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1002-2610_1002-260 others(14): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | ||||||
chr7:107686441 | C | CTTTCTTT others(7): Show |
21 | a0001c0001t0001g0119 a0001c0001t0001g0135 a0001c0001t0001g0136 others(18): Show |
21 | HG01074.hp2 HG01099.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.1002-2609_1002-259 others(18): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | ||||||
chr7:107686441 | C | CTTTCTTT others(11): Show |
38 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0018 others(35): Show |
38 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(22): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | ||||||
chr7:107686441 | C | CTTTCTTT others(15): Show |
43 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(40): Show |
44 | HG00280.hp1 HG00408.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(26): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | ||||||
chr7:107686441 | C | CTTTCTTT others(19): Show |
41 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0026 others(38): Show |
41 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(30): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | ||||||
chr7:107686441 | C | CTTTCTTT others(30): Show |
1 | a0001c0001t0001g0225 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(41): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | ||||||
chr7:107686441 | C | CTTTCTTT others(23): Show |
16 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0056 others(13): Show |
17 | HG00544.hp1 HG00642.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(34): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | ||||||
chr7:107686441 | C | CTTTCTTT others(27): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(8): Show |
11 | HG00735.hp2 HG01099.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(38): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | ||||||
chr7:107686441 | C | CTTTCTTT others(31): Show |
5 | a0001c0001t0001g0012 a0001c0001t0001g0153 a0001c0001t0001g0233 others(2): Show |
5 | HG00741.hp1 HG01109.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(42): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | ||||||
chr7:107686441 | C | CTTTCTTT others(39): Show |
1 | a0001c0001t0001g0218 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(50): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | ||||||
chr7:107686442 | T | TTTCTTTC others(12): Show |
1 | a0001c0001t0005g0327 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(23): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686442 | ||||||
chr7:107686442 | T | TTTCTTTC others(16): Show |
1 | a0001c0001t0001g0204 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(27): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686442 | ||||||
chr7:107686442 | T | TTTCTTTC others(24): Show |
2 | a0001c0001t0001g0086 a0001c0001t0001g0122 |
2 | HG01081.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(35): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686442 | ||||||
chr7:107686443 | T | TTCTTTCT others(15): Show |
1 | a0001c0001t0001g0169 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(26): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686443 | ||||||
chr7:107686443 | T | TTCTTTCT others(19): Show |
3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0095 |
3 | NA19010.hp1 NA19063.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(30): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686443 | ||||||
chr7:107686443 | T | TTCTTTCT others(23): Show |
1 | a0001c0001t0001g0039 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(34): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686443 | ||||||
chr7:107686443 | T | TTCTTTCT others(27): Show |
1 | a0001c0001t0006g0094 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(38): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686443 | ||||||
chr7:107686454 | T | TTTCTTCT others(21): Show |
1 | a0001c0001t0005g0293 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(32): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686454 | ||||||
chr7:107686464 | T | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG00642.hp1 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1002-2589T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686464 | |||||||
chr7:107686557 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(182): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1002-2496G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686557 | |||||||
chr7:107686599 | T | C | 5 | a0002c0002t0013g0084 a0006c0008t0014g0063 a0006c0008t0030g0042 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-2454T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686599 | |||||||
chr7:107686600 | G | A | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1002-2453G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686600 | |||||||
chr7:107686623 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002-2430G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686623 | |||||||
chr7:107686663 | A | T | 2 | a0001c0011t0007g0323 a0001c0011t0007g0324 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1002-2390A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686663 | |||||||
chr7:107686736 | T | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1002-2317T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686736 | |||||||
chr7:107686790 | T | C | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1002-2263T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686790 | |||||||
chr7:107686829 | C | G | 1 | a0001c0001t0003g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002-2224C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686829 | |||||||
chr7:107686900 | C | T | 1 | a0002c0002t0018g0020 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1002-2153C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686900 | |||||||
chr7:107686961 | T | C | 1 | a0001c0001t0002g0272 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1002-2092T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686961 | |||||||
chr7:107687296 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1002-1757G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107687296 | |||||||
chr7:107687386 | C | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0112 a0001c0001t0001g0167 others(1): Show |
4 | HG00597.hp1 NA18970.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-1667C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107687386 | |||||||
chr7:107687407 | C | T | 106 | a0001c0001t0001g0247 a0001c0001t0001g0259 a0001c0001t0001g0284 others(103): Show |
108 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1002-1646C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107687407 | |||||||
chr7:107687504 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1002-1549A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107687504 | |||||||
chr7:107687870 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(184): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1002-1183G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107687870 | |||||||
chr7:107688038 | TTAGG | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0056 others(13): Show |
17 | HG01106.hp1 HG02071.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1002-1010_1002-100 others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107688038 | ||||||
chr7:107688039 | T | C | 1 | a0001c0001t0009g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1002-1014T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688039 | |||||||
chr7:107688051 | C | A | 1 | a0001c0001t0003g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002-1002C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688051 | |||||||
chr7:107688092 | A | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(309): Show |
322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1002-961A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688092 | |||||||
chr7:107688213 | C | G | 7 | a0001c0001t0009g0068 a0001c0001t0009g0190 a0001c0011t0007g0323 others(4): Show |
7 | HG02257.hp1 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1002-840C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688213 | |||||||
chr7:107688252 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1002-801A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688252 | |||||||
chr7:107688288 | G | A | 2 | a0001c0001t0002g0073 a0001c0001t0002g0263 |
2 | NA18963.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1002-765G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688288 | |||||||
chr7:107688369 | T | G | 20 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0031 others(17): Show |
21 | HG00140.hp2 HG00735.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.1002-684T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688369 | |||||||
chr7:107688511 | G | A | 2 | a0001c0001t0001g0332 a0001c0001t0001g0346 |
2 | HG01069.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1002-542G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688511 | |||||||
chr7:107688677 | A | T | 1 | a0001c0001t0007g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1002-376A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688677 | |||||||
chr7:107689367 | G | C | 1 | a0001c0001t0003g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1149+167G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/20 | chr7 | 107689367 | |||||||
chr7:107689391 | T | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0188 a0001c0001t0001g0192 |
3 | HG02896.hp2 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1149+191T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/20 | chr7 | 107689391 | |||||||
chr7:107689484 | G | T | 2 | a0001c0001t0001g0178 a0001c0001t0003g0193 |
2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1149+284G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/20 | chr7 | 107689484 | |||||||
chr7:107689536 | T | A | 5 | a0001c0001t0007g0184 a0003c0003t0003g0022 a0003c0003t0003g0027 others(2): Show |
5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149+336T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/20 | chr7 | 107689536 | |||||||
chr7:107689671 | C | T | 3 | a0001c0019t0001g0174 a0002c0009t0024g0196 a0002c0009t0025g0311 |
3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1150-453C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/20 | chr7 | 107689671 | |||||||
chr7:107689989 | C | T | 15 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0076 others(12): Show |
15 | HG00280.hp2 HG00323.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1150-135C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/20 | chr7 | 107689989 | |||||||
chr7:107690556 | T | C | 7 | a0001c0001t0009g0068 a0001c0001t0009g0190 a0001c0011t0007g0323 others(4): Show |
7 | HG02257.hp1 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1263+319T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107690556 | |||||||
chr7:107690646 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0211 others(1): Show |
4 | HG00140.hp1 HG00639.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263+409C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107690646 | |||||||
chr7:107691108 | T | TAC | 28 | a0001c0001t0001g0029 a0001c0001t0001g0070 a0001c0001t0001g0194 others(25): Show |
29 | HG00438.hp1 HG00438.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1263+905_1263+906d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | ||||||
chr7:107691108 | T | TACAC | 104 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
109 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1263+903_1263+906d others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | ||||||
chr7:107691108 | T | TACACAC | 112 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0086 others(109): Show |
115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1263+901_1263+906d others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | ||||||
chr7:107691108 | T | TACACACA others(1): Show |
43 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(40): Show |
43 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.1263+899_1263+906d others(10): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | ||||||
chr7:107691108 | T | TACACACA others(3): Show |
13 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0126 others(10): Show |
14 | HG00621.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1263+897_1263+906d others(12): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | ||||||
chr7:107691108 | T | TACACACA others(5): Show |
4 | a0001c0001t0001g0047 a0001c0001t0001g0127 a0001c0001t0001g0178 others(1): Show |
4 | HG00621.hp2 HG01928.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263+895_1263+906d others(14): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | ||||||
chr7:107691108 | TAC | T | 11 | a0001c0001t0001g0223 a0001c0001t0001g0329 a0001c0001t0003g0171 others(8): Show |
11 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1263+905_1263+906d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | ||||||
chr7:107691144 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0255 a0001c0001t0005g0008 |
3 | NA18960.hp1 NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1263+907T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691144 | |||||||
chr7:107691167 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(176): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1263+930C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691167 | |||||||
chr7:107691218 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1263+981T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691218 | |||||||
chr7:107691256 | C | T | 6 | a0001c0001t0001g0338 a0001c0001t0007g0335 a0001c0001t0007g0337 others(3): Show |
6 | HG02055.hp2 HG03209.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1263+1019C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691256 | |||||||
chr7:107691276 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0353 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1263+1039C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691276 | |||||||
chr7:107691307 | A | G | 1 | a0001c0001t0004g0164 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1263+1070A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691307 | |||||||
chr7:107691426 | T | C | 2 | a0001c0001t0003g0179 a0001c0001t0007g0197 |
2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1263+1189T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691426 | |||||||
chr7:107691481 | G | A | 1 | a0001c0001t0006g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1263+1244G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691481 | |||||||
chr7:107691504 | A | AAT | 96 | a0001c0001t0001g0259 a0001c0001t0001g0284 a0001c0001t0002g0002 others(93): Show |
98 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1263+1277_1263+127 others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691504 | ||||||
chr7:107691510 | T | TACACACA others(3): Show |
1 | a0001c0001t0001g0056 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1263+1274_1263+127 others(14): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691510 | ||||||
chr7:107691512 | T | C | 19 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0057 others(16): Show |
19 | HG00597.hp1 HG01891.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.1263+1275T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691512 | |||||||
chr7:107691512 | T | TACACACA others(3): Show |
13 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0147 others(10): Show |
14 | HG01106.hp1 HG02155.hp2 NA18953.hp2 others(11): Show |
intron_variant | MODIFIER | c.1263+1276_1263+127 others(14): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691512 | ||||||
chr7:107691514 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1263+1277T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691514 | |||||||
chr7:107691514 | T | TAC | 3 | a0001c0001t0003g0037 a0001c0001t0003g0179 a0001c0001t0007g0197 |
3 | HG03139.hp2 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1263+1307_1263+130 others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691514 | ||||||
chr7:107691514 | T | TACAC | 4 | a0001c0001t0007g0184 a0003c0003t0003g0022 a0003c0003t0003g0176 others(1): Show |
4 | HG02922.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263+1305_1263+130 others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691514 | ||||||
chr7:107691514 | T | TACACACA others(7): Show |
1 | a0003c0003t0003g0027 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1263+1295_1263+130 others(18): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691514 | ||||||
chr7:107691514 | T | TATAC | 5 | a0001c0001t0002g0274 a0001c0001t0004g0235 a0001c0001t0004g0254 others(2): Show |
5 | HG00544.hp2 HG02451.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+1278_1263+127 others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691514 | ||||||
chr7:107691514 | T | TATACAC | 5 | a0001c0001t0002g0061 a0001c0001t0002g0089 a0001c0001t0002g0111 others(2): Show |
5 | HG01123.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+1278_1263+127 others(10): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691514 | ||||||
chr7:107691514 | T | TATACACA others(3): Show |
2 | a0001c0001t0001g0178 a0001c0001t0003g0193 |
2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1263+1278_1263+127 others(14): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691514 | ||||||
chr7:107691516 | C | T | 2 | a0001c0001t0004g0054 a0002c0002t0013g0084 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1263+1279C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691516 | |||||||
chr7:107691546 | A | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(258): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1263+1309A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691546 | |||||||
chr7:107691548 | C | A | 101 | a0001c0001t0001g0178 a0001c0001t0001g0259 a0001c0001t0001g0284 others(98): Show |
103 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1263+1311C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691548 | |||||||
chr7:107691548 | C | CACAA | 9 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(6): Show |
9 | HG00597.hp1 HG00642.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1263+1312_1263+131 others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | ||||||
chr7:107691548 | C | CACACAA | 19 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0039 others(16): Show |
19 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1263+1312_1263+131 others(10): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | ||||||
chr7:107691548 | C | CACACACA others(1): Show |
85 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1263+1312_1263+131 others(12): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | ||||||
chr7:107691548 | C | CACACACA others(3): Show |
30 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0017 others(27): Show |
32 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1263+1312_1263+131 others(14): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | ||||||
chr7:107691548 | C | CACACACA others(4): Show |
1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1263+1312_1263+131 others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | ||||||
chr7:107691548 | C | CACACACA others(5): Show |
8 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0058 others(5): Show |
8 | HG03130.hp2 HG03491.hp2 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.1263+1312_1263+131 others(16): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | ||||||
chr7:107691548 | C | CACACACA others(6): Show |
2 | a0001c0001t0007g0337 a0001c0001t0013g0334 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1263+1312_1263+131 others(17): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | ||||||
chr7:107691548 | C | CACACACA others(7): Show |
1 | a0001c0001t0007g0335 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1263+1312_1263+131 others(18): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | ||||||
chr7:107691548 | C | CACACACA others(9): Show |
1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1263+1312_1263+131 others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | ||||||
chr7:107691548 | CAT | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0056 others(17): Show |
21 | HG01106.hp1 HG01358.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1263+1328_1263+132 others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | ||||||
chr7:107691550 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(256): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1263+1313T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691550 | |||||||
chr7:107691552 | T | TATATATA others(9): Show |
3 | a0001c0001t0004g0235 a0001c0001t0004g0254 a0001c0001t0004g0305 |
3 | NA18939.hp1 NA18992.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1263+1327_1263+132 others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691552 | ||||||
chr7:107691565 | A | T | 1 | a0001c0001t0012g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1263+1328A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691565 | |||||||
chr7:107691566 | T | C | 1 | a0001c0001t0012g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1263+1329T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691566 | |||||||
chr7:107691569 | T | A | 1 | a0001c0001t0012g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1263+1332T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691569 | |||||||
chr7:107691570 | C | T | 1 | a0001c0001t0012g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1263+1333C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691570 | |||||||
chr7:107691776 | T | A | 1 | a0001c0001t0028g0227 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1263+1539T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691776 | |||||||
chr7:107691777 | A | T | 1 | a0001c0001t0028g0227 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1263+1540A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691777 | |||||||
chr7:107691778 | T | A | 1 | a0001c0001t0028g0227 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1263+1541T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691778 | |||||||
chr7:107692029 | C | T | 2 | a0001c0001t0003g0251 a0001c0001t0005g0246 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1263+1792C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692029 | |||||||
chr7:107692058 | G | A | 2 | a0001c0001t0003g0134 a0001c0001t0008g0198 |
2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1263+1821G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692058 | |||||||
chr7:107692148 | T | C | 1 | a0001c0019t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1263+1911T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692148 | |||||||
chr7:107692151 | C | T | 1 | a0001c0019t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1263+1914C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692151 | |||||||
chr7:107692650 | A | T | 2 | a0001c0001t0003g0005 a0001c0001t0019g0189 |
3 | HG02486.hp2 HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1264-1753A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692650 | |||||||
chr7:107692869 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(184): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1264-1534A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692869 | |||||||
chr7:107692944 | A | T | 1 | a0001c0001t0028g0227 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1264-1459A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692944 | |||||||
chr7:107693133 | A | G | 2 | a0001c0001t0002g0103 a0001c0001t0002g0128 |
2 | HG00558.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1264-1270A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693133 | |||||||
chr7:107693176 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1264-1227C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693176 | |||||||
chr7:107693177 | G | A | 2 | a0002c0002t0018g0020 a0013c0015t0018g0187 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1264-1226G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693177 | |||||||
chr7:107693256 | T | A | 1 | a0001c0001t0028g0227 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1264-1147T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693256 | |||||||
chr7:107693425 | G | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0202 a0001c0001t0005g0146 |
3 | NA18983.hp2 NA19011.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1264-978G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693425 | |||||||
chr7:107693553 | GCTT | G | 8 | a0001c0001t0001g0139 a0001c0001t0003g0005 a0001c0001t0003g0134 others(5): Show |
9 | HG02258.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264-847_1264-845d others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107693553 | ||||||
chr7:107693558 | T | A | 1 | a0001c0001t0002g0318 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1264-845T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693558 | |||||||
chr7:107693581 | C | T | 105 | a0001c0001t0001g0259 a0001c0001t0001g0284 a0001c0001t0002g0002 others(102): Show |
107 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1264-822C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693581 | |||||||
chr7:107693738 | C | T | 2 | a0001c0001t0002g0270 a0001c0001t0002g0274 |
2 | HG00544.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1264-665C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693738 | |||||||
chr7:107694068 | T | A | 105 | a0001c0001t0001g0259 a0001c0001t0001g0284 a0001c0001t0002g0002 others(102): Show |
107 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1264-335T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107694068 | |||||||
chr7:107694216 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1264-187C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107694216 | |||||||
chr7:107694527 | T | C | 11 | a0001c0001t0001g0047 a0001c0001t0001g0091 a0001c0001t0001g0133 others(8): Show |
11 | HG02083.hp2 HG02135.hp1 HG03834.hp1 others(8): Show |
intron_variant | MODIFIER | c.1341+47T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 11/20 | chr7 | 107694527 | |||||||
chr7:107694903 | T | G | 4 | a0006c0008t0014g0063 a0006c0008t0030g0042 a0007c0010t0003g0180 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1437+187T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107694903 | |||||||
chr7:107694959 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0211 others(2): Show |
5 | HG00140.hp1 HG00639.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.1437+243T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107694959 | |||||||
chr7:107695180 | T | C | 1 | a0001c0001t0031g0175 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1437+464T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107695180 | |||||||
chr7:107695613 | C | A | 99 | a0001c0001t0001g0259 a0001c0001t0001g0284 a0001c0001t0002g0002 others(96): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1438-320C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107695613 | |||||||
chr7:107695675 | G | T | 4 | a0006c0008t0014g0063 a0006c0008t0030g0042 a0007c0010t0003g0180 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1438-258G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107695675 | |||||||
chr7:107695779 | C | T | 5 | a0001c0001t0003g0037 a0001c0001t0005g0351 a0001c0001t0008g0036 others(2): Show |
5 | HG00642.hp2 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1438-154C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107695779 | |||||||
chr7:107695919 | A | G | 2 | a0002c0002t0018g0020 a0013c0015t0018g0187 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1438-14A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107695919 | |||||||
chr7:107696135 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 |
4 | HG02015.hp2 NA18980.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1544+96C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696135 | |||||||
chr7:107696248 | G | T | 1 | a0001c0001t0007g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1544+209G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696248 | |||||||
chr7:107696308 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1544+269G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696308 | |||||||
chr7:107696333 | T | C | 1 | a0001c0001t0001g0029 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1544+294T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696333 | |||||||
chr7:107696431 | T | A | 2 | a0002c0002t0018g0020 a0013c0015t0018g0187 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1544+392T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696431 | |||||||
chr7:107696437 | T | G | 9 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0172 others(6): Show |
10 | HG00140.hp2 HG00735.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.1544+398T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696437 | |||||||
chr7:107696465 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1544+426C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696465 | |||||||
chr7:107696482 | C | A | 1 | a0003c0003t0003g0027 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1544+443C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696482 | |||||||
chr7:107696701 | A | G | 1 | a0001c0001t0005g0327 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1544+662A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696701 | |||||||
chr7:107696813 | G | T | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1544+774G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696813 | |||||||
chr7:107696950 | C | T | 2 | a0002c0009t0024g0196 a0002c0009t0025g0311 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1544+911C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696950 | |||||||
chr7:107696951 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0071 others(2): Show |
6 | HG03225.hp2 HG03471.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1544+912G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696951 | |||||||
chr7:107697012 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1544+973A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107697012 | |||||||
chr7:107697123 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0200 |
2 | HG00408.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1545-919C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107697123 | |||||||
chr7:107697865 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1545-177A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107697865 | |||||||
chr7:107697894 | A | G | 1 | a0001c0001t0028g0227 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1545-148A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107697894 | |||||||
chr7:107698037 | T | G | 2 | a0002c0002t0018g0020 a0013c0015t0018g0187 |
2 | HG02109.hp1 HG03139.hp1 |
splice_region_variant&intron_variant | LOW | c.1545-5T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107698037 | |||||||
chr7:107698316 | G | A | 1 | a0001c0011t0007g0324 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1614+205G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698316 | |||||||
chr7:107698539 | A | G | 2 | a0001c0001t0016g0100 a0001c0001t0016g0340 |
2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1614+428A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698539 | |||||||
chr7:107698554 | T | A | 1 | a0001c0001t0002g0273 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1614+443T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698554 | |||||||
chr7:107698563 | C | T | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1614+452C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698563 | |||||||
chr7:107698606 | T | C | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1614+495T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698606 | |||||||
chr7:107698651 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1614+540G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698651 | |||||||
chr7:107698702 | T | G | 1 | a0001c0001t0027g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1614+591T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698702 | |||||||
chr7:107698733 | G | A | 2 | a0001c0001t0002g0261 a0001c0001t0002g0308 |
2 | HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1614+622G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698733 | |||||||
chr7:107699017 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG00642.hp1 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1614+906G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699017 | |||||||
chr7:107699054 | T | C | 2 | a0002c0002t0018g0020 a0013c0015t0018g0187 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1614+943T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699054 | |||||||
chr7:107699220 | A | C | 2 | a0001c0001t0016g0100 a0001c0001t0016g0340 |
2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1615-863A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699220 | |||||||
chr7:107699466 | G | A | 299 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(296): Show |
309 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1615-617G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699466 | |||||||
chr7:107699562 | C | G | 1 | a0001c0022t0006g0060 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1615-521C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699562 | |||||||
chr7:107699574 | G | A | 2 | a0006c0008t0014g0063 a0006c0008t0030g0042 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1615-509G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699574 | |||||||
chr7:107699597 | T | TCCAAGAG others(45): Show |
1 | a0001c0001t0001g0142 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1615-484_1615-433d others(54): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr7 | 107699597 | ||||||
chr7:107699656 | C | T | 5 | a0001c0001t0002g0245 a0001c0001t0002g0277 a0001c0001t0002g0278 others(2): Show |
5 | HG02015.hp1 HG02135.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-427C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699656 | |||||||
chr7:107699657 | G | A | 1 | a0001c0001t0002g0250 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1615-426G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699657 | |||||||
chr7:107699693 | C | T | 1 | a0001c0001t0008g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1615-390C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699693 | |||||||
chr7:107699700 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1615-383G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699700 | |||||||
chr7:107699927 | CA | C | 6 | a0002c0009t0024g0196 a0002c0009t0025g0311 a0006c0008t0014g0063 others(3): Show |
6 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-140delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr7 | 107699927 | ||||||
chr7:107699927 | CAA | C | 19 | a0001c0001t0001g0228 a0001c0001t0002g0032 a0001c0001t0002g0033 others(16): Show |
19 | HG00280.hp2 HG00323.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1615-141_1615-140d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr7 | 107699927 | ||||||
chr7:107699927 | CAAA | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(277): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1615-142_1615-140d others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr7 | 107699927 | ||||||
chr7:107699930 | A | C | 1 | a0001c0001t0002g0168 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1615-153A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699930 | |||||||
chr7:107699969 | C | A | 1 | a0001c0001t0005g0313 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-114C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699969 | |||||||
chr7:107700180 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18954.hp2 | splice_region_variant&intron_variant | LOW | c.1707+5G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 15/20 | chr7 | 107700180 | |||||||
chr7:107700251 | G | C | 9 | a0002c0002t0013g0084 a0002c0002t0018g0020 a0002c0009t0024g0196 others(6): Show |
9 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1707+76G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 15/20 | chr7 | 107700251 | |||||||
chr7:107700386 | T | C | 9 | a0002c0002t0013g0084 a0002c0002t0018g0020 a0002c0009t0024g0196 others(6): Show |
9 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1707+211T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 15/20 | chr7 | 107700386 | |||||||
chr7:107701083 | T | A | 3 | a0001c0001t0002g0076 a0001c0001t0002g0215 a0001c0001t0002g0234 |
3 | HG00323.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1708-18T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 15/20 | chr7 | 107701083 | |||||||
chr7:107701670 | A | C | 1 | a0001c0001t0003g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1804-157A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 16/20 | chr7 | 107701670 | |||||||
chr7:107701740 | T | G | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1804-87T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 16/20 | chr7 | 107701740 | |||||||
chr7:107701821 | G | A | 1 | a0001c0001t0002g0304 | 1 | HG02056.hp2 | splice_region_variant&intron_variant | LOW | c.1804-6G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 16/20 | chr7 | 107701821 | |||||||
chr7:107702110 | T | C | 2 | a0002c0009t0024g0196 a0002c0009t0025g0311 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2034+53T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702110 | |||||||
chr7:107702189 | G | A | 4 | a0003c0003t0003g0022 a0003c0003t0003g0027 a0003c0003t0003g0176 others(1): Show |
4 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2034+132G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702189 | |||||||
chr7:107702224 | C | G | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2034+167C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702224 | |||||||
chr7:107702430 | G | A | 2 | a0002c0002t0018g0020 a0013c0015t0018g0187 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2034+373G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702430 | |||||||
chr7:107702445 | A | G | 1 | a0003c0003t0003g0027 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2034+388A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702445 | |||||||
chr7:107702518 | C | T | 1 | a0001c0001t0003g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2034+461C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702518 | |||||||
chr7:107702642 | G | A | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2034+585G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702642 | |||||||
chr7:107702684 | C | CA | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(175): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.2034+645dupA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr7 | 107702684 | ||||||
chr7:107702807 | C | A | 3 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 |
3 | HG01074.hp2 HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2034+750C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702807 | |||||||
chr7:107702871 | G | T | 1 | a0004c0004t0009g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2034+814G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702871 | |||||||
chr7:107702943 | G | A | 5 | a0002c0002t0013g0084 a0002c0002t0018g0020 a0002c0009t0024g0196 others(2): Show |
5 | HG01074.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2034+886G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702943 | |||||||
chr7:107703095 | T | A | 1 | a0001c0001t0027g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2034+1038T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703095 | |||||||
chr7:107703164 | T | C | 3 | a0003c0003t0003g0022 a0003c0003t0003g0176 a0003c0003t0003g0177 |
3 | HG02922.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2034+1107T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703164 | |||||||
chr7:107703317 | C | G | 101 | a0001c0001t0001g0228 a0001c0001t0001g0259 a0001c0001t0001g0284 others(98): Show |
103 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2035-1014C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703317 | |||||||
chr7:107703327 | A | T | 1 | a0013c0015t0018g0187 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2035-1004A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703327 | |||||||
chr7:107703410 | G | A | 1 | a0001c0001t0002g0308 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2035-921G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703410 | |||||||
chr7:107703469 | C | G | 2 | a0002c0009t0024g0196 a0002c0009t0025g0311 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2035-862C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703469 | |||||||
chr7:107703490 | G | T | 1 | a0001c0001t0002g0310 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2035-841G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703490 | |||||||
chr7:107703564 | A | G | 4 | a0006c0008t0014g0063 a0006c0008t0030g0042 a0007c0010t0003g0180 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2035-767A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703564 | |||||||
chr7:107703588 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(171): Show |
181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.2035-743A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703588 | |||||||
chr7:107703753 | A | G | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2035-578A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703753 | |||||||
chr7:107703771 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(168): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.2035-560C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703771 | |||||||
chr7:107703772 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(305): Show |
318 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.2035-559T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703772 | |||||||
chr7:107704109 | T | C | 2 | a0002c0002t0018g0020 a0013c0015t0018g0187 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2035-222T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107704109 | |||||||
chr7:107704121 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(172): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.2035-210C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107704121 | |||||||
chr7:107704508 | T | C | 2 | a0002c0002t0018g0020 a0013c0015t0018g0187 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2089+123T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704508 | |||||||
chr7:107704539 | C | T | 1 | a0001c0001t0006g0267 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2089+154C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704539 | |||||||
chr7:107704563 | T | C | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2089+178T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704563 | |||||||
chr7:107704720 | A | T | 4 | a0001c0001t0009g0068 a0004c0004t0009g0013 a0004c0004t0009g0024 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089+335A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704720 | |||||||
chr7:107704739 | C | A | 2 | a0001c0001t0001g0151 a0001c0001t0005g0146 |
2 | NA18983.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2089+354C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704739 | |||||||
chr7:107704806 | T | C | 3 | a0001c0001t0003g0248 a0008c0007t0003g0303 a0008c0007t0003g0348 |
3 | HG02698.hp2 HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2089+421T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704806 | |||||||
chr7:107704946 | C | T | 1 | a0001c0001t0002g0322 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2089+561C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704946 | |||||||
chr7:107704947 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(187): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.2089+562G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704947 | |||||||
chr7:107705001 | G | A | 1 | a0001c0001t0007g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2089+616G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107705001 | |||||||
chr7:107705341 | G | A | 2 | a0001c0001t0002g0002 a0005c0005t0002g0159 |
3 | HG03491.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2089+956G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107705341 | |||||||
chr7:107705642 | G | GT | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(191): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.2089+1259dupT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr7 | 107705642 | ||||||
chr7:107705765 | C | A | 9 | a0002c0002t0013g0084 a0002c0002t0018g0020 a0002c0009t0024g0196 others(6): Show |
9 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2089+1380C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107705765 | |||||||
chr7:107705825 | C | T | 2 | a0002c0009t0024g0196 a0002c0009t0025g0311 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2089+1440C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107705825 | |||||||
chr7:107705946 | T | C | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+1561T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107705946 | |||||||
chr7:107705997 | A | G | 1 | a0001c0001t0009g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2089+1612A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107705997 | |||||||
chr7:107706086 | T | C | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+1701T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706086 | |||||||
chr7:107706091 | C | T | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+1706C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706091 | |||||||
chr7:107706180 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2089+1795C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706180 | |||||||
chr7:107706217 | G | A | 3 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 |
3 | HG01074.hp2 HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2089+1832G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706217 | |||||||
chr7:107706305 | T | A | 11 | a0002c0002t0013g0084 a0002c0002t0014g0349 a0002c0002t0014g0350 others(8): Show |
11 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2089+1920T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706305 | |||||||
chr7:107706314 | A | G | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+1929A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706314 | |||||||
chr7:107706329 | G | T | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+1944G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706329 | |||||||
chr7:107706477 | A | C | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+2092A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706477 | |||||||
chr7:107706512 | T | C | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2089+2127T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706512 | |||||||
chr7:107706597 | C | T | 3 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 |
3 | HG01074.hp2 HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2089+2212C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706597 | |||||||
chr7:107706608 | G | C | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+2223G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706608 | |||||||
chr7:107706629 | T | C | 2 | a0002c0002t0018g0020 a0013c0015t0018g0187 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2089+2244T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706629 | |||||||
chr7:107706645 | C | T | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+2260C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706645 | |||||||
chr7:107706669 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2089+2284C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706669 | |||||||
chr7:107706752 | C | CT | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+2368dupT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr7 | 107706752 | ||||||
chr7:107706795 | G | C | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+2410G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706795 | |||||||
chr7:107706804 | C | T | 4 | a0006c0008t0014g0063 a0006c0008t0030g0042 a0007c0010t0003g0180 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2089+2419C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706804 | |||||||
chr7:107706805 | A | G | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+2420A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706805 | |||||||
chr7:107706907 | C | T | 5 | a0001c0001t0003g0179 a0001c0001t0007g0197 a0001c0001t0016g0100 others(2): Show |
5 | HG01433.hp2 HG02615.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.2089+2522C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706907 | |||||||
chr7:107707019 | A | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0163 others(1): Show |
4 | HG03225.hp2 HG03540.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2089+2634A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707019 | |||||||
chr7:107707154 | T | C | 3 | a0005c0005t0002g0159 a0007c0010t0003g0180 a0007c0010t0005g0183 |
3 | HG02559.hp2 HG02723.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2089+2769T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707154 | |||||||
chr7:107707158 | C | G | 1 | a0002c0002t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2089+2773C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707158 | |||||||
chr7:107707338 | T | C | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-2716T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707338 | |||||||
chr7:107707349 | C | A | 1 | a0001c0001t0001g0346 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2090-2705C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707349 | |||||||
chr7:107707351 | A | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(187): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.2090-2703A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707351 | |||||||
chr7:107707417 | A | T | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-2637A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707417 | |||||||
chr7:107707456 | C | T | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-2598C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707456 | |||||||
chr7:107707522 | T | A | 6 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2090-2532T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707522 | |||||||
chr7:107707544 | G | A | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-2510G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707544 | |||||||
chr7:107707605 | A | G | 2 | a0002c0009t0024g0196 a0002c0009t0025g0311 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2090-2449A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707605 | |||||||
chr7:107707617 | A | G | 1 | a0001c0001t0002g0304 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2090-2437A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707617 | |||||||
chr7:107707659 | G | A | 3 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 |
3 | HG01074.hp2 HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2090-2395G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707659 | |||||||
chr7:107707789 | C | T | 2 | a0002c0009t0024g0196 a0002c0009t0025g0311 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2090-2265C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707789 | |||||||
chr7:107707793 | T | C | 2 | a0001c0001t0002g0105 a0001c0001t0002g0157 |
2 | HG00558.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.2090-2261T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707793 | |||||||
chr7:107707875 | G | T | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2090-2179G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707875 | |||||||
chr7:107707927 | C | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(193): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.2090-2127C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707927 | |||||||
chr7:107707963 | A | G | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-2091A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707963 | |||||||
chr7:107708053 | A | G | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-2001A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708053 | |||||||
chr7:107708233 | A | G | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1821A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708233 | |||||||
chr7:107708283 | G | T | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1771G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708283 | |||||||
chr7:107708310 | G | A | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2090-1744G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708310 | |||||||
chr7:107708315 | G | T | 2 | a0001c0001t0008g0143 a0001c0001t0021g0352 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2090-1739G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708315 | |||||||
chr7:107708419 | A | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0065 a0001c0001t0001g0255 others(1): Show |
4 | NA18960.hp1 NA18977.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.2090-1635A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708419 | |||||||
chr7:107708445 | T | C | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1609T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708445 | |||||||
chr7:107708555 | T | A | 11 | a0002c0002t0013g0084 a0002c0002t0014g0349 a0002c0002t0014g0350 others(8): Show |
11 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2090-1499T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708555 | |||||||
chr7:107708682 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2090-1372C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708682 | |||||||
chr7:107708685 | C | G | 4 | a0001c0001t0003g0179 a0001c0001t0007g0197 a0001c0001t0016g0100 others(1): Show |
4 | HG01433.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2090-1369C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708685 | |||||||
chr7:107708702 | T | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0188 others(2): Show |
5 | HG02896.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2090-1352T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708702 | |||||||
chr7:107708702 | TA | T | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1346delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr7 | 107708702 | ||||||
chr7:107708703 | A | T | 5 | a0001c0001t0003g0248 a0001c0001t0003g0266 a0001c0001t0003g0315 others(2): Show |
5 | HG01884.hp1 HG02698.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.2090-1351A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708703 | |||||||
chr7:107708704 | A | T | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1350A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708704 | |||||||
chr7:107708827 | A | G | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1227A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708827 | |||||||
chr7:107708840 | G | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.2090-1214G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708840 | |||||||
chr7:107708847 | G | A | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1207G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708847 | |||||||
chr7:107708953 | G | A | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2090-1101G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708953 | |||||||
chr7:107708958 | T | G | 1 | a0001c0001t0001g0219 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2090-1096T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708958 | |||||||
chr7:107708974 | G | T | 1 | a0001c0001t0001g0049 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2090-1080G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708974 | |||||||
chr7:107709018 | C | T | 4 | a0001c0001t0002g0010 a0001c0001t0002g0270 a0001c0001t0002g0274 others(1): Show |
4 | HG00544.hp2 HG02071.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.2090-1036C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709018 | |||||||
chr7:107709027 | G | A | 4 | a0001c0001t0009g0068 a0004c0004t0009g0013 a0004c0004t0009g0024 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2090-1027G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709027 | |||||||
chr7:107709035 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2090-1019A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709035 | |||||||
chr7:107709147 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0119 |
2 | HG00597.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.2090-907C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709147 | |||||||
chr7:107709282 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2090-772T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709282 | |||||||
chr7:107709582 | G | T | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-472G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709582 | |||||||
chr7:107709661 | G | A | 2 | a0001c0001t0002g0280 a0001c0001t0002g0333 |
2 | NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2090-393G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709661 | |||||||
chr7:107709678 | C | T | 1 | a0001c0001t0002g0322 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2090-376C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709678 | |||||||
chr7:107709720 | T | C | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-334T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709720 | |||||||
chr7:107709858 | G | T | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2090-196G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709858 | |||||||
chr7:107709868 | GC | G | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-183delC | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr7 | 107709868 | ||||||
chr7:107709900 | G | A | 2 | a0002c0002t0018g0020 a0013c0015t0018g0187 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2090-154G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709900 | |||||||
chr7:107709944 | A | C | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-110A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709944 | |||||||
chr7:107709994 | A | AAAAC | 14 | a0001c0001t0027g0144 a0002c0002t0013g0084 a0002c0002t0014g0349 others(11): Show |
14 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2090-52_2090-49dup others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr7 | 107709994 | ||||||
chr7:107710047 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03540.hp1 | splice_region_variant&intron_variant | LOW | c.2090-7T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107710047 | |||||||
chr7:107710328 | G | GT | 7 | a0002c0002t0013g0084 a0002c0009t0024g0196 a0002c0009t0025g0311 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2235+135dupT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 107710328 | ||||||
chr7:107710353 | A | G | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2235+154A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710353 | |||||||
chr7:107710505 | C | T | 2 | a0002c0002t0014g0349 a0002c0002t0014g0350 |
2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2235+306C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710505 | |||||||
chr7:107710587 | G | A | 1 | a0004c0004t0009g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2235+388G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710587 | |||||||
chr7:107710645 | A | G | 1 | a0001c0001t0002g0320 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2235+446A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710645 | |||||||
chr7:107710666 | T | A | 1 | a0001c0001t0027g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2235+467T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710666 | |||||||
chr7:107710719 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0353 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2235+520A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710719 | |||||||
chr7:107710890 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2235+691A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710890 | |||||||
chr7:107710978 | G | A | 6 | a0002c0009t0024g0196 a0002c0009t0025g0311 a0006c0008t0014g0063 others(3): Show |
6 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2235+779G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710978 | |||||||
chr7:107711073 | GGA | G | 4 | a0001c0001t0003g0179 a0001c0001t0007g0197 a0001c0001t0016g0100 others(1): Show |
4 | HG01433.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2235+879_2235+880d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 107711073 | ||||||
chr7:107711152 | GA | G | 8 | a0001c0001t0001g0023 a0001c0001t0001g0150 a0001c0001t0001g0153 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2235+965delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 107711152 | ||||||
chr7:107711436 | A | G | 1 | a0001c0001t0004g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2236-1103A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107711436 | |||||||
chr7:107711503 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2236-1036G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107711503 | |||||||
chr7:107711672 | G | A | 98 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(95): Show |
100 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.2236-867G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107711672 | |||||||
chr7:107711766 | G | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0097 a0001c0001t0001g0200 |
3 | HG00408.hp1 NA18957.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.2236-773G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107711766 | |||||||
chr7:107711784 | C | G | 1 | a0001c0001t0016g0100 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2236-755C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107711784 | |||||||
chr7:107711954 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2236-585T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107711954 | |||||||
chr7:107712010 | T | A | 1 | a0001c0001t0001g0329 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2236-529T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107712010 | |||||||
chr7:107712112 | T | G | 1 | a0001c0001t0007g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2236-427T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107712112 | |||||||
chr7:107712193 | G | C | 1 | a0001c0001t0031g0175 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2236-346G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107712193 | |||||||
chr7:107712374 | T | C | 2 | a0002c0009t0024g0196 a0002c0009t0025g0311 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2236-165T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107712374 | |||||||
chr7:107712388 | G | T | 6 | a0002c0009t0024g0196 a0002c0009t0025g0311 a0006c0008t0014g0063 others(3): Show |
6 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2236-151G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107712388 | |||||||
chr7:107712683 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2319+61C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107712683 | |||||||
chr7:107713159 | G | A | 9 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
9 | HG00544.hp1 HG00621.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.2319+537G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713159 | |||||||
chr7:107713367 | T | A | 4 | a0003c0003t0003g0022 a0003c0003t0003g0027 a0003c0003t0003g0176 others(1): Show |
4 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2319+745T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713367 | |||||||
chr7:107713569 | G | A | 2 | a0002c0009t0024g0196 a0002c0009t0025g0311 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2319+947G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713569 | |||||||
chr7:107713588 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(182): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.2319+966C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713588 | |||||||
chr7:107713638 | C | T | 4 | a0006c0008t0014g0063 a0006c0008t0030g0042 a0007c0010t0003g0180 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2319+1016C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713638 | |||||||
chr7:107713640 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2319+1018A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713640 | |||||||
chr7:107713688 | A | G | 2 | a0002c0009t0024g0196 a0002c0009t0025g0311 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2319+1066A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713688 | |||||||
chr7:107713909 | G | T | 1 | a0001c0001t0001g0006 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2319+1287G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713909 | |||||||
chr7:107713909 | GTAT | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(194): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.2319+1307_2319+130 others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107713909 | ||||||
chr7:107714005 | C | T | 1 | a0001c0001t0002g0322 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2319+1383C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714005 | |||||||
chr7:107714085 | AT | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(319): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.2320-1326delT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107714085 | ||||||
chr7:107714275 | G | A | 4 | a0001c0001t0001g0247 a0001c0001t0003g0251 a0001c0001t0003g0252 others(1): Show |
4 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2320-1148G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714275 | |||||||
chr7:107714430 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2320-993G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714430 | |||||||
chr7:107714471 | G | A | 1 | a0001c0001t0012g0283 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2320-952G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714471 | |||||||
chr7:107714568 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2320-855C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714568 | |||||||
chr7:107714626 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2320-797G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714626 | |||||||
chr7:107714902 | C | A | 1 | a0001c0001t0012g0271 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2320-521C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714902 | |||||||
chr7:107715066 | T | TA | 9 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0172 others(6): Show |
9 | HG00140.hp2 HG00621.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2320-338dupA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | ||||||
chr7:107715066 | T | TAAA | 8 | a0001c0001t0003g0101 a0001c0001t0003g0179 a0003c0003t0003g0022 others(5): Show |
8 | HG02559.hp2 HG02723.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2320-340_2320-338d others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | ||||||
chr7:107715066 | T | TAAAAAAA others(6): Show |
5 | a0001c0001t0002g0286 a0001c0001t0007g0184 a0001c0001t0007g0337 others(2): Show |
5 | HG02015.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2320-350_2320-338d others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | ||||||
chr7:107715066 | T | TAAAAAAA others(7): Show |
39 | a0001c0001t0002g0002 a0001c0001t0002g0032 a0001c0001t0002g0033 others(36): Show |
40 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.2320-351_2320-338d others(16): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | ||||||
chr7:107715066 | T | TAAAAAAA others(8): Show |
26 | a0001c0001t0002g0083 a0001c0001t0002g0092 a0001c0001t0002g0103 others(23): Show |
26 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.2320-352_2320-338d others(17): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | ||||||
chr7:107715066 | T | TAAAAAAA others(9): Show |
7 | a0001c0001t0002g0010 a0001c0001t0002g0081 a0001c0001t0002g0258 others(4): Show |
7 | HG00544.hp2 HG04184.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.2320-353_2320-338d others(18): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | ||||||
chr7:107715066 | T | TAAAAAAA others(10): Show |
3 | a0001c0001t0002g0270 a0001c0001t0004g0235 a0001c0001t0004g0254 |
3 | HG02071.hp2 NA18939.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.2320-354_2320-338d others(19): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | ||||||
chr7:107715066 | T | TAAAAAAA others(11): Show |
8 | a0001c0001t0002g0030 a0001c0001t0002g0124 a0001c0001t0002g0168 others(5): Show |
8 | HG01070.hp1 HG01993.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.2320-355_2320-338d others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | ||||||
chr7:107715066 | T | TAAAAAAA others(12): Show |
10 | a0001c0001t0002g0011 a0001c0001t0002g0073 a0001c0001t0002g0173 others(7): Show |
11 | HG01255.hp2 HG01978.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.2320-356_2320-338d others(21): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | ||||||
chr7:107715066 | T | TAAAAAAA others(13): Show |
3 | a0001c0001t0004g0264 a0001c0001t0004g0306 a0016c0018t0002g0034 |
3 | NA18980.hp1 NA18987.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2320-338_2320-337i others(22): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | ||||||
chr7:107715066 | T | TAAAAAAA others(14): Show |
1 | a0001c0001t0002g0079 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2320-338_2320-337i others(23): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | ||||||
chr7:107715066 | TA | T | 7 | a0001c0001t0001g0122 a0001c0001t0001g0238 a0001c0001t0006g0094 others(4): Show |
8 | HG01081.hp2 HG01993.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.2320-338delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | ||||||
chr7:107715237 | C | A | 1 | a0001c0001t0001g0041 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2320-186C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715237 | |||||||
chr7:107715237 | C | CAA | 15 | a0001c0001t0009g0068 a0001c0001t0009g0190 a0001c0001t0010g0003 others(12): Show |
16 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2320-173_2320-172d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715237 | ||||||
chr7:107715300 | T | C | 2 | a0002c0002t0018g0020 a0013c0015t0018g0187 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2320-123T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715300 | |||||||
chr7:107715312 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-111A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715312 | |||||||
chr7:107715314 | G | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-109G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715314 | |||||||
chr7:107715315 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-108A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715315 | |||||||
chr7:107715316 | G | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-107G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715316 | |||||||
chr7:107715319 | G | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-104G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715319 | |||||||
chr7:107715321 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-102A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715321 | |||||||
chr7:107715322 | G | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-101G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715322 | |||||||
chr7:107715324 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-99A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715324 | |||||||
chr7:107715325 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-98A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715325 | |||||||
chr7:107715326 | G | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-97G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715326 | |||||||
chr7:107715331 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-92C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715331 | |||||||
chr7:107715332 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-91A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715332 | |||||||
chr7:107715333 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-90A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715333 | |||||||
chr7:107715335 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-88A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715335 | |||||||
chr7:107715340 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-83A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715340 | |||||||
chr7:107715341 | A | C | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-82A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715341 | |||||||
chr7:107715342 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-81A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715342 | |||||||
chr7:107715344 | A | G | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-79A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715344 | |||||||
chr7:107715345 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-78C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715345 | |||||||
chr7:107715346 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-77A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715346 | |||||||
chr7:107715348 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-75A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715348 | |||||||
chr7:107715351 | T | G | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-72T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715351 | |||||||
chr7:107715352 | A | G | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-71A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715352 | |||||||
chr7:107715354 | A | C | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-69A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715354 | |||||||
chr7:107715355 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-68A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715355 | |||||||
chr7:107715356 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-67A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715356 | |||||||
chr7:107715357 | A | C | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-66A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715357 | |||||||
chr7:107715358 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-65A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715358 | |||||||
chr7:107715360 | G | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-63G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715360 | |||||||
chr7:107715361 | A | C | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-62A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715361 | |||||||
chr7:107715363 | A | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-60A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715363 | |||||||
chr7:107715364 | A | C | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-59A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715364 | |||||||
chr7:107715366 | G | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-57G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715366 | |||||||
chr7:107715367 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-56C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715367 | |||||||
chr7:107715370 | A | C | 1 | a0001c0001t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-53A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715370 | |||||||
chr7:107715401 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0005g0325 |
3 | HG00140.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2320-22T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715401 |