Item | Value |
---|---|
geneid | 9498 |
ensemblid | ENSG00000050438.17 |
hgncid | 11034 |
symbol | SLC4A8 |
name | solute carrier family 4 member 8 |
refseq_nuc | NM_001039960.3 |
refseq_prot | NP_001035049.1 |
ensembl_nuc | ENST00000453097.7 |
ensembl_prot | ENSP00000405812.2 |
mane_status | MANE Select |
chr | chr12 |
start | 51424831 |
end | 51515763 |
strand | + |
ver | v1.2 |
region | chr12:51424831-51515763 |
region5000 | chr12:51419831-51520763 |
regionname0 | SLC4A8_chr12_51424831_51515763 |
regionname5000 | SLC4A8_chr12_51419831_51520763 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1093 | 353 | 90 | 59 | 154 | 14 | 34 | 114 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | MPAAG others(1088): Show |
chr12 | 51419831 | 51520763 |
a0002 | 0/0 | 1093 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | MPAAG others(1088): Show |
chr12 | 51419831 | 51520763 |
a0003 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | MPAAG others(1088): Show |
chr12 | 51419831 | 51520763 |
a0004 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | MPAAG others(1088): Show |
chr12 | 51419831 | 51520763 |
a0005 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | MPAAG others(1088): Show |
chr12 | 51419831 | 51520763 |
a0006 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | MPAAG others(1088): Show |
chr12 | 51419831 | 51520763 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3279 | 312 | 71 | 57 | 138 | 14 | 30 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0001c0002 | 0/0 | 3279 | 26 | 10 | 0 | 14 | 0 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0001c0003 | 0/0 | 3279 | 7 | 7 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0001c0004 | 0/0 | 3279 | 2 | 0 | 2 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0001c0005 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0001c0006 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0001c0008 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0001c0010 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0001c0011 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0001c0014 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0002c0007 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0003c0009 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0004c0012 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0005c0013 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 | ||
a0006c0015 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | ATGCC others(3274): Show |
chr12 | 51419831 | 51520763 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 11762 | 94 | 14 | 21 | 47 | 4 | 8 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0002 | 0/1 | 11763 | 64 | 10 | 20 | 16 | 6 | 11 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0003 | 1/0 | 11764 | 39 | 8 | 7 | 17 | 2 | 4 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0004 | 0/0 | 11763 | 34 | 3 | 2 | 26 | 1 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0006 | 0/0 | 11763 | 8 | 8 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0007 | 0/0 | 11763 | 5 | 1 | 0 | 4 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0008 | 0/0 | 11762 | 5 | 5 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0009 | 0/0 | 11762 | 5 | 5 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0011 | 0/0 | 11762 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0012 | 0/0 | 11762 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0013 | 0/0 | 11764 | 2 | 0 | 1 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0014 | 0/0 | 11763 | 3 | 2 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0015 | 0/0 | 11763 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0016 | 0/0 | 11765 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11760): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0017 | 0/0 | 11762 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0018 | 0/0 | 11762 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0019 | 0/0 | 11762 | 2 | 0 | 0 | 0 | 0 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0020 | 0/0 | 11762 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0021 | 0/0 | 11764 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0022 | 0/0 | 11763 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0023 | 0/0 | 11762 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0024 | 0/0 | 11763 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0025 | 0/0 | 11764 | 2 | 1 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0026 | 0/0 | 11762 | 2 | 0 | 0 | 0 | 1 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0028 | 0/0 | 11762 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0029 | 0/0 | 11762 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0030 | 0/0 | 11762 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0031 | 0/0 | 11762 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0032 | 0/0 | 11762 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0033 | 0/0 | 11762 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0034 | 0/0 | 11762 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0035 | 0/0 | 11762 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0037 | 0/0 | 11764 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0038 | 0/0 | 11764 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0039 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0040 | 0/0 | 11762 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0041 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0042 | 0/0 | 11763 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0043 | 0/0 | 11763 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0048 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0049 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0050 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0051 | 0/0 | 11763 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0052 | 0/0 | 11763 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0001t0053 | 0/0 | 11762 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0002t0005 | 0/0 | 11763 | 18 | 3 | 0 | 13 | 0 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0002t0010 | 0/0 | 11764 | 4 | 4 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0001c0002t0027 | 0/0 | 11763 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0002t0044 | 0/0 | 11763 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0002t0045 | 0/0 | 11764 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0001c0003t0005 | 0/0 | 11763 | 6 | 6 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0003t0046 | 0/0 | 11762 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0004t0002 | 0/0 | 11763 | 2 | 0 | 2 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0005t0005 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0006t0002 | 0/0 | 11763 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0008t0036 | 0/0 | 11764 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0001c0010t0001 | 0/0 | 11762 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0001c0011t0047 | 0/0 | 11763 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11758): Show |
chr12 | 51419831 | 51520763 |
a0001c0014t0003 | 0/0 | 11764 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0002c0007t0003 | 0/0 | 11764 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0003c0009t0013 | 0/0 | 11764 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0004c0012t0001 | 0/0 | 11762 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
a0005c0013t0003 | 0/0 | 11764 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11759): Show |
chr12 | 51419831 | 51520763 |
a0006c0015t0001 | 0/0 | 11762 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | GCGGG others(11757): Show |
chr12 | 51419831 | 51520763 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0326 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0006g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0007g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0008g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0008g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0011g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0011g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0012g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0012g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0012g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0013g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0013g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0014g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0014g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0015g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0015g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0015g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0016g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0016g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0016g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0017g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0017g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0018g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0018g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0019g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0020g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0020g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0021g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0021g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0022g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0022g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0023g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0023g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0024g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0024g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0025g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0025g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0026g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0026g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0028g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0029g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0030g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0031g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0032g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0033g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0034g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0035g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0037g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0038g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0039g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0040g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0041g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0042g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0043g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0048g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0049g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0050g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0051g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0052g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0001t0053g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0010g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0010g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0010g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0027g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0027g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0044g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0002t0045g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0003t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0003t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0003t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0003t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0003t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0003t0046g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0004t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0004t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0005t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0006t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0008t0036g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0010t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0011t0047g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0001c0014t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0002c0007t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0003c0009t0013g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0004c0012t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0005c0013t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
a0006c0015t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | GBR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0126 | EUR | GBR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | FIN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0314 | EUR | FIN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00423 | hp1 | a0001 | c0001 | t0032 | g0292 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00544 | hp2 | a0001 | c0001 | t0048 | g0027 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00558 | hp2 | a0001 | c0002 | t0005 | g0165 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00609 | hp1 | a0001 | c0001 | t0015 | g0111 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0329 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00639 | hp2 | a0001 | c0001 | t0031 | g0254 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00642 | hp2 | a0001 | c0001 | t0013 | g0001 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | CHS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00733 | hp2 | a0001 | c0001 | t0030 | g0191 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0306 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01081 | hp1 | a0001 | c0004 | t0002 | g0122 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0060 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01192 | hp2 | a0001 | c0001 | t0035 | g0214 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0318 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0319 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01261 | hp2 | a0001 | c0004 | t0002 | g0130 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0321 | EUR | IBS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0134 | EUR | IBS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0058 | EUR | IBS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0121 | EUR | IBS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01517 | hp1 | a0001 | c0001 | t0026 | g0059 | EUR | IBS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01884 | hp1 | a0001 | c0001 | t0037 | g0339 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01884 | hp2 | a0001 | c0002 | t0010 | g0024 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01891 | hp1 | a0001 | c0002 | t0010 | g0154 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01891 | hp2 | a0001 | c0001 | t0025 | g0031 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01928 | hp2 | a0002 | c0007 | t0003 | g0304 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0309 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01978 | hp2 | a0001 | c0001 | t0014 | g0104 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02015 | hp2 | a0001 | c0001 | t0039 | g0094 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02055 | hp2 | a0001 | c0001 | t0021 | g0157 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02056 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02071 | hp1 | a0001 | c0001 | t0025 | g0028 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02071 | hp2 | a0001 | c0002 | t0005 | g0160 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02083 | hp1 | a0001 | c0002 | t0005 | g0164 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CDX | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CDX | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02257 | hp1 | a0001 | c0002 | t0027 | g0293 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02258 | hp1 | a0001 | c0003 | t0005 | g0180 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0249 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02300 | hp2 | a0001 | c0001 | t0034 | g0217 | AMR | PEL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02572 | hp1 | a0001 | c0003 | t0005 | g0183 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0089 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0091 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02615 | hp2 | a0001 | c0002 | t0005 | g0159 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02622 | hp2 | a0001 | c0006 | t0002 | g0138 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02630 | hp1 | a0001 | c0001 | t0009 | g0076 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02630 | hp2 | a0001 | c0003 | t0005 | g0008 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0296 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02723 | hp1 | a0001 | c0002 | t0044 | g0295 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02723 | hp2 | a0001 | c0003 | t0005 | g0008 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02735 | hp1 | a0001 | c0014 | t0003 | g0320 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02809 | hp1 | a0001 | c0001 | t0022 | g0155 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0287 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02818 | hp1 | a0001 | c0001 | t0023 | g0075 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0090 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02886 | hp2 | a0001 | c0002 | t0005 | g0178 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0083 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02895 | hp2 | a0001 | c0002 | t0010 | g0153 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02896 | hp2 | a0001 | c0003 | t0005 | g0182 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02897 | hp1 | a0001 | c0002 | t0010 | g0152 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02897 | hp2 | a0001 | c0003 | t0046 | g0184 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0255 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02970 | hp2 | a0001 | c0001 | t0014 | g0021 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02976 | hp1 | a0001 | c0001 | t0020 | g0324 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02976 | hp2 | a0001 | c0001 | t0014 | g0020 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0327 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03098 | hp1 | a0001 | c0001 | t0040 | g0147 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0275 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03130 | hp1 | a0001 | c0001 | t0020 | g0325 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0084 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03225 | hp1 | a0001 | c0008 | t0036 | g0073 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03453 | hp1 | a0001 | c0001 | t0008 | g0282 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03453 | hp2 | a0001 | c0003 | t0005 | g0181 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03486 | hp1 | a0001 | c0001 | t0009 | g0087 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03516 | hp2 | a0001 | c0001 | t0033 | g0253 | AFR | ESN | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03669 | hp1 | a0001 | c0001 | t0019 | g0012 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0043 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03704 | hp2 | a0001 | c0001 | t0019 | g0012 | SAS | PJL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03831 | hp1 | a0001 | c0002 | t0005 | g0172 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03831 | hp2 | a0001 | c0001 | t0051 | g0062 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0322 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03927 | hp2 | a0001 | c0010 | t0001 | g0216 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0291 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0061 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG04204 | hp1 | a0001 | c0001 | t0052 | g0057 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG04204 | hp2 | a0001 | c0002 | t0005 | g0161 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG04228 | hp1 | a0001 | c0001 | t0026 | g0036 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | STU | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | YRI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18522 | hp2 | a0004 | c0012 | t0001 | g0019 | AFR | YRI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | CHB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0064 | AFR | YRI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18906 | hp2 | a0001 | c0001 | t0021 | g0158 | AFR | YRI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18941 | hp2 | a0001 | c0002 | t0005 | g0166 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18943 | hp1 | a0001 | c0001 | t0041 | g0124 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18943 | hp2 | a0001 | c0001 | t0016 | g0338 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18944 | hp1 | a0001 | c0001 | t0050 | g0052 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18944 | hp2 | a0001 | c0001 | t0038 | g0004 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18946 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18950 | hp2 | a0001 | c0002 | t0005 | g0170 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18953 | hp2 | a0001 | c0001 | t0015 | g0110 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18962 | hp1 | a0001 | c0002 | t0005 | g0171 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18963 | hp2 | a0001 | c0001 | t0016 | g0046 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18966 | hp2 | a0001 | c0002 | t0005 | g0177 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18970 | hp1 | a0001 | c0001 | t0049 | g0045 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18974 | hp1 | a0001 | c0001 | t0015 | g0077 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0252 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18978 | hp1 | a0001 | c0001 | t0012 | g0265 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18978 | hp2 | a0001 | c0005 | t0005 | g0162 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18979 | hp1 | a0001 | c0001 | t0011 | g0197 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18979 | hp2 | a0001 | c0002 | t0005 | g0168 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18981 | hp2 | a0001 | c0001 | t0024 | g0128 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18983 | hp2 | a0001 | c0002 | t0005 | g0176 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18988 | hp2 | a0001 | c0002 | t0005 | g0173 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18989 | hp2 | a0001 | c0001 | t0018 | g0281 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18997 | hp1 | a0001 | c0011 | t0047 | g0169 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18997 | hp2 | a0001 | c0001 | t0013 | g0097 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19004 | hp1 | a0001 | c0001 | t0017 | g0269 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19004 | hp2 | a0001 | c0001 | t0011 | g0199 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19011 | hp2 | a0005 | c0013 | t0003 | g0303 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19012 | hp1 | a0001 | c0001 | t0028 | g0237 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19012 | hp2 | a0001 | c0002 | t0005 | g0167 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19030 | hp1 | a0001 | c0001 | t0008 | g0203 | AFR | LWK | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19030 | hp2 | a0001 | c0001 | t0053 | g0088 | AFR | LWK | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | LWK | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19054 | hp2 | a0001 | c0001 | t0018 | g0270 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19056 | hp2 | a0001 | c0001 | t0011 | g0198 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19060 | hp2 | a0001 | c0001 | t0012 | g0210 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19063 | hp1 | a0006 | c0015 | t0001 | g0331 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19068 | hp1 | a0001 | c0002 | t0005 | g0175 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19072 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19078 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19079 | hp1 | a0001 | c0002 | t0005 | g0163 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19079 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19080 | hp1 | a0001 | c0001 | t0012 | g0278 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19081 | hp2 | a0001 | c0001 | t0017 | g0266 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19082 | hp2 | a0001 | c0001 | t0016 | g0337 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19086 | hp2 | a0001 | c0001 | t0024 | g0137 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0148 | AFR | YRI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0142 | EUR | TSI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | TSI | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | GIH | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0323 | SAS | GIH | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01123 | hp1 | a0001 | c0001 | t0029 | g0274 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02109 | hp1 | a0001 | c0002 | t0005 | g0179 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02486 | hp1 | a0003 | c0009 | t0013 | g0082 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG02559 | hp2 | a0001 | c0001 | t0023 | g0149 | AFR | ACB | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG03471 | hp2 | a0001 | c0001 | t0022 | g0156 | AFR | MSL | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG06807 | hp1 | a0001 | c0001 | t0043 | g0151 | AFR | USA | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
HG06807 | hp2 | a0001 | c0002 | t0027 | g0294 | AFR | USA | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA18955 | hp2 | a0001 | c0002 | t0045 | g0174 | EAS | JPT | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | USA | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | USA | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | LWK | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
NA21309 | hp2 | a0001 | c0001 | t0042 | g0150 | AFR | LWK | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0085 | REF | REF | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0326 | REF | REF | SLC4A8_chr12_51419831_51520763 | SLC4A8 | chr12 | 51419831 | 51520763 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:51457438 | A | G | 1 | a0006 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.662A>G | p.His221Arg | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 6/25 | 819/11764 | 662/3282 | 221/1093 | chr12 | 51457438 | |||
chr12:51462342 | G | T | 1 | a0005 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.1134G>T | p.Glu378Asp | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/25 | 1291/11764 | 1134/3282 | 378/1093 | chr12 | 51462342 | |||
chr12:51462443 | A | G | 1 | a0004 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.1235A>G | p.Asn412Ser | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/25 | 1392/11764 | 1235/3282 | 412/1093 | chr12 | 51462443 | |||
chr12:51474421 | G | A | 1 | a0002 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1984G>A | p.Val662Ile | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 15/25 | 2141/11764 | 1984/3282 | 662/1093 | chr12 | 51474421 | |||
chr12:51489943 | A | G | 1 | a0003 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2692A>G | p.Ile898Val | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/25 | 2849/11764 | 2692/3282 | 898/1093 | chr12 | 51489943 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:51450910 | G | C | 1 | a0001c0005 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.165G>C | p.Pro55Pro | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/25 | 322/11764 | 165/3282 | 55/1093 | chr12 | 51450910 | |||
chr12:51460076 | C | G | 1 | a0001c0003 | 7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
synonymous_variant | LOW | c.981C>G | p.Leu327Leu | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/25 | 1138/11764 | 981/3282 | 327/1093 | chr12 | 51460076 | |||
chr12:51461225 | T | G | 1 | a0001c0006 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1035T>G | p.Gly345Gly | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/25 | 1192/11764 | 1035/3282 | 345/1093 | chr12 | 51461225 | |||
chr12:51461276 | C | G | 1 | a0001c0014 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.1086C>G | p.Thr362Thr | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/25 | 1243/11764 | 1086/3282 | 362/1093 | chr12 | 51461276 | |||
chr12:51462375 | C | T | 1 | a0001c0004 | 2 | HG01081.hp1 HG01261.hp2 |
synonymous_variant | LOW | c.1167C>T | p.Phe389Phe | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/25 | 1324/11764 | 1167/3282 | 389/1093 | chr12 | 51462375 | |||
chr12:51469653 | C | G | 4 | a0001c0002 a0001c0003 a0001c0005 others(1): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
synonymous_variant | LOW | c.1389C>G | p.Ala463Ala | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 12/25 | 1546/11764 | 1389/3282 | 463/1093 | chr12 | 51469653 | |||
chr12:51469759 | C | T | 4 | a0001c0002 a0001c0003 a0001c0005 others(1): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
synonymous_variant | LOW | c.1495C>T | p.Leu499Leu | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 12/25 | 1652/11764 | 1495/3282 | 499/1093 | chr12 | 51469759 | |||
chr12:51488788 | C | G | 1 | a0001c0010 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.2376C>G | p.Leu792Leu | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/25 | 2533/11764 | 2376/3282 | 792/1093 | chr12 | 51488788 | |||
chr12:51489915 | G | C | 1 | a0001c0008 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.2664G>C | p.Leu888Leu | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/25 | 2821/11764 | 2664/3282 | 888/1093 | chr12 | 51489915 | |||
chr12:51494977 | C | T | 4 | a0001c0002 a0001c0003 a0001c0005 others(1): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
synonymous_variant | LOW | c.2802C>T | p.Pro934Pro | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/25 | 2959/11764 | 2802/3282 | 934/1093 | chr12 | 51494977 | |||
chr12:51494986 | C | T | 1 | a0001c0011 | 1 | NA18997.hp1 | synonymous_variant | LOW | c.2811C>T | p.His937His | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/25 | 2968/11764 | 2811/3282 | 937/1093 | chr12 | 51494986 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:51424884 | G | T | 1 | a0001c0002t0027 | 2 | HG02257.hp1 HG06807.hp2 |
5_prime_UTR_variant | MODIFIER | c.-104G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/25 | 104 | chr12 | 51424884 | ||||||
chr12:51507606 | A | G | 35 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(32): Show |
179 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*168A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 168 | chr12 | 51507606 | ||||||
chr12:51507651 | A | T | 2 | a0001c0001t0009 a0001c0001t0053 |
6 | HG02572.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*213A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 213 | chr12 | 51507651 | ||||||
chr12:51507914 | G | C | 15 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(12): Show |
96 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*476G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 476 | chr12 | 51507914 | ||||||
chr12:51508031 | C | T | 1 | a0001c0001t0038 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*593C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 593 | chr12 | 51508031 | ||||||
chr12:51508211 | T | C | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(56): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*773T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 773 | chr12 | 51508211 | ||||||
chr12:51508257 | T | C | 1 | a0001c0001t0039 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 819 | chr12 | 51508257 | ||||||
chr12:51508414 | C | T | 2 | a0001c0001t0021 a0001c0001t0022 |
4 | HG02055.hp2 HG02809.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*976C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 976 | chr12 | 51508414 | ||||||
chr12:51508440 | AG | A | 20 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(17): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1004delG | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 1004 | INFO_REALIGN_3_PRIME | chr12 | 51508440 | |||||
chr12:51508465 | C | T | 10 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0016 others(7): Show |
49 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1027C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 1027 | chr12 | 51508465 | ||||||
chr12:51508469 | A | ATT | 1 | a0001c0001t0016 | 3 | NA18943.hp2 NA18963.hp2 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1032_*1033insTT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 1033 | INFO_REALIGN_3_PRIME | chr12 | 51508469 | |||||
chr12:51508717 | T | C | 1 | a0001c0001t0028 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1279T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 1279 | chr12 | 51508717 | ||||||
chr12:51509087 | C | T | 1 | a0001c0001t0015 | 3 | HG00609.hp1 NA18953.hp2 NA18974.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1649C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 1649 | chr12 | 51509087 | ||||||
chr12:51509420 | C | T | 1 | a0001c0001t0035 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1982C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 1982 | chr12 | 51509420 | ||||||
chr12:51509721 | C | G | 1 | a0001c0001t0011 | 3 | NA18979.hp1 NA19004.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2283C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2283 | chr12 | 51509721 | ||||||
chr12:51509768 | T | C | 1 | a0001c0001t0040 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2330T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2330 | chr12 | 51509768 | ||||||
chr12:51509831 | A | T | 3 | a0001c0001t0021 a0001c0001t0022 a0001c0001t0037 |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2393A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2393 | chr12 | 51509831 | ||||||
chr12:51509896 | G | A | 1 | a0001c0002t0010 | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2458G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2458 | chr12 | 51509896 | ||||||
chr12:51509953 | G | A | 2 | a0001c0001t0042 a0001c0001t0043 |
2 | HG06807.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2515G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2515 | chr12 | 51509953 | ||||||
chr12:51509954 | A | T | 2 | a0001c0001t0042 a0001c0001t0043 |
2 | HG06807.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2516A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2516 | chr12 | 51509954 | ||||||
chr12:51509979 | G | A | 2 | a0001c0002t0027 a0001c0002t0044 |
3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2541G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2541 | chr12 | 51509979 | ||||||
chr12:51510060 | C | T | 1 | a0001c0001t0052 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2622C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2622 | chr12 | 51510060 | ||||||
chr12:51510076 | C | G | 11 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0013 others(8): Show |
87 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2638C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2638 | chr12 | 51510076 | ||||||
chr12:51510152 | C | T | 1 | a0001c0001t0034 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2714C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2714 | chr12 | 51510152 | ||||||
chr12:51510241 | G | A | 1 | a0001c0008t0036 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2803G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2803 | chr12 | 51510241 | ||||||
chr12:51510253 | C | T | 1 | a0001c0011t0047 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2815C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 2815 | chr12 | 51510253 | ||||||
chr12:51510423 | CA | C | 44 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(41): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*3006delA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3006 | INFO_REALIGN_3_PRIME | chr12 | 51510423 | |||||
chr12:51510423 | CAA | C | 6 | a0001c0001t0009 a0001c0001t0023 a0001c0001t0026 others(3): Show |
12 | HG01517.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3005_*3006delAA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3005 | INFO_REALIGN_3_PRIME | chr12 | 51510423 | |||||
chr12:51510456 | G | A | 1 | a0001c0001t0029 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3018G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3018 | chr12 | 51510456 | ||||||
chr12:51510858 | G | A | 1 | a0001c0001t0048 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3420G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3420 | chr12 | 51510858 | ||||||
chr12:51511032 | C | T | 25 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(22): Show |
143 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*3594C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3594 | chr12 | 51511032 | ||||||
chr12:51511075 | T | C | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(56): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*3637T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3637 | chr12 | 51511075 | ||||||
chr12:51511167 | T | C | 1 | a0001c0001t0053 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3729T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3729 | chr12 | 51511167 | ||||||
chr12:51511247 | G | A | 1 | a0001c0001t0050 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3809G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3809 | chr12 | 51511247 | ||||||
chr12:51511401 | T | A | 2 | a0001c0001t0014 a0001c0001t0029 |
4 | HG01123.hp1 HG01978.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3963T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 3963 | chr12 | 51511401 | ||||||
chr12:51511593 | T | C | 1 | a0001c0001t0037 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4155T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 4155 | chr12 | 51511593 | ||||||
chr12:51511824 | C | T | 8 | a0001c0002t0005 a0001c0002t0027 a0001c0002t0044 others(5): Show |
31 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*4386C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 4386 | chr12 | 51511824 | ||||||
chr12:51511879 | G | A | 1 | a0001c0001t0030 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4441G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 4441 | chr12 | 51511879 | ||||||
chr12:51511891 | C | T | 1 | a0001c0001t0024 | 2 | NA18981.hp2 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4453C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 4453 | chr12 | 51511891 | ||||||
chr12:51512261 | G | A | 25 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(22): Show |
143 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*4823G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 4823 | chr12 | 51512261 | ||||||
chr12:51512296 | G | C | 1 | a0001c0001t0017 | 2 | NA19004.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4858G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 4858 | chr12 | 51512296 | ||||||
chr12:51512457 | T | C | 1 | a0001c0001t0041 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5019T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5019 | chr12 | 51512457 | ||||||
chr12:51512513 | C | G | 1 | a0001c0001t0033 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5075C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5075 | chr12 | 51512513 | ||||||
chr12:51512565 | C | A | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(56): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*5127C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5127 | chr12 | 51512565 | ||||||
chr12:51512736 | T | G | 1 | a0001c0001t0051 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5298T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5298 | chr12 | 51512736 | ||||||
chr12:51512962 | G | T | 1 | a0001c0001t0006 | 8 | HG02895.hp1 HG02922.hp1 HG03130.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5524G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5524 | chr12 | 51512962 | ||||||
chr12:51512980 | T | G | 1 | a0001c0001t0018 | 2 | NA18989.hp2 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5542T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5542 | chr12 | 51512980 | ||||||
chr12:51513216 | G | A | 1 | a0001c0001t0019 | 2 | HG03669.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5778G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5778 | chr12 | 51513216 | ||||||
chr12:51513400 | T | C | 35 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(32): Show |
179 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*5962T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5962 | chr12 | 51513400 | ||||||
chr12:51513414 | G | A | 25 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(22): Show |
143 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*5976G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 5976 | chr12 | 51513414 | ||||||
chr12:51513643 | T | C | 1 | a0001c0002t0010 | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6205T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 6205 | chr12 | 51513643 | ||||||
chr12:51513699 | C | T | 1 | a0001c0001t0043 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6261C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 6261 | chr12 | 51513699 | ||||||
chr12:51513896 | C | A | 1 | a0001c0002t0010 | 4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6458C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 6458 | chr12 | 51513896 | ||||||
chr12:51513969 | A | G | 1 | a0001c0001t0032 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6531A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 6531 | chr12 | 51513969 | ||||||
chr12:51514509 | T | G | 1 | a0001c0001t0031 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7071T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 7071 | chr12 | 51514509 | ||||||
chr12:51514820 | G | A | 11 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0013 others(8): Show |
87 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*7382G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 7382 | chr12 | 51514820 | ||||||
chr12:51514879 | G | C | 1 | a0001c0001t0020 | 2 | HG02976.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7441G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 7441 | chr12 | 51514879 | ||||||
chr12:51514912 | G | A | 1 | a0001c0001t0008 | 5 | HG02258.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7474G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 7474 | chr12 | 51514912 | ||||||
chr12:51515055 | C | T | 1 | a0001c0002t0027 | 2 | HG02257.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7617C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 7617 | chr12 | 51515055 | ||||||
chr12:51515348 | G | C | 20 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(17): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*7910G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 25/25 | 7910 | chr12 | 51515348 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:51425044 | CCGCCTCC others(2): Show |
C | 4 | a0001c0001t0004g0336 a0001c0001t0016g0337 a0001c0001t0016g0338 others(1): Show |
4 | HG01884.hp1 NA18943.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+20_48+28delGCCT others(5): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51425044 | ||||||
chr12:51425106 | T | A | 4 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+71T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425106 | |||||||
chr12:51425142 | TC | T | 5 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(2): Show |
5 | HG02523.hp1 NA18962.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+110delC | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51425142 | ||||||
chr12:51425250 | G | C | 4 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+215G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425250 | |||||||
chr12:51425255 | T | C | 2 | a0001c0001t0014g0020 a0001c0001t0014g0021 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.48+220T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425255 | |||||||
chr12:51425365 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.48+330C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425365 | |||||||
chr12:51425643 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG00642.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.48+608G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425643 | |||||||
chr12:51425670 | G | C | 1 | a0001c0002t0010g0024 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.48+635G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425670 | |||||||
chr12:51425848 | A | C | 1 | a0004c0012t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.48+813A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425848 | |||||||
chr12:51425900 | C | T | 1 | a0001c0001t0003g0329 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.48+865C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51425900 | |||||||
chr12:51426128 | C | G | 1 | a0001c0001t0002g0328 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.48+1093C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426128 | |||||||
chr12:51426170 | G | A | 302 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.48+1135G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426170 | |||||||
chr12:51426331 | C | T | 3 | a0001c0002t0027g0293 a0001c0002t0027g0294 a0001c0002t0044g0295 |
3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.48+1296C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426331 | |||||||
chr12:51426496 | G | A | 46 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(43): Show |
46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.48+1461G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426496 | |||||||
chr12:51426715 | G | A | 6 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+1680G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426715 | |||||||
chr12:51426827 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.48+1792G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426827 | |||||||
chr12:51426920 | ATTTTCTT others(9): Show |
A | 1 | a0001c0001t0032g0292 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.48+1901_48+1916del others(16): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51426920 | ||||||
chr12:51426941 | CT | C | 6 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(3): Show |
6 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.48+1921delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51426941 | ||||||
chr12:51426995 | G | T | 1 | a0001c0001t0002g0291 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.48+1960G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51426995 | |||||||
chr12:51427026 | T | C | 180 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(177): Show |
187 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.48+1991T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427026 | |||||||
chr12:51427095 | C | A | 1 | a0001c0001t0003g0296 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.48+2060C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427095 | |||||||
chr12:51427174 | G | A | 1 | a0001c0001t0004g0026 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.48+2139G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427174 | |||||||
chr12:51427221 | A | G | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+2186A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427221 | |||||||
chr12:51427755 | A | G | 21 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(18): Show |
21 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.48+2720A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427755 | |||||||
chr12:51427831 | C | T | 1 | a0001c0002t0005g0179 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.48+2796C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427831 | |||||||
chr12:51427897 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.48+2862C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427897 | |||||||
chr12:51427900 | A | G | 39 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(36): Show |
40 | HG00558.hp2 HG01884.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.48+2865A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51427900 | |||||||
chr12:51428043 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | NA18952.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.48+3008C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428043 | |||||||
chr12:51428141 | A | G | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+3106A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428141 | |||||||
chr12:51428259 | C | G | 47 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(44): Show |
47 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.48+3224C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428259 | |||||||
chr12:51428435 | A | G | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+3400A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428435 | |||||||
chr12:51428481 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.48+3446A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428481 | |||||||
chr12:51428591 | A | T | 47 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(44): Show |
47 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.48+3556A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428591 | |||||||
chr12:51428660 | A | G | 49 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(46): Show |
49 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.48+3625A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51428660 | |||||||
chr12:51429023 | C | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | HG00621.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.48+3988C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429023 | |||||||
chr12:51429234 | G | A | 1 | a0001c0001t0023g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.48+4199G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429234 | |||||||
chr12:51429242 | G | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+4207G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429242 | |||||||
chr12:51429261 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.48+4226G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429261 | |||||||
chr12:51429335 | A | G | 1 | a0001c0001t0001g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.48+4300A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429335 | |||||||
chr12:51429459 | C | T | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+4424C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429459 | |||||||
chr12:51429516 | T | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+4481T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429516 | |||||||
chr12:51429584 | C | T | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.48+4549C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429584 | |||||||
chr12:51429613 | C | G | 1 | a0001c0001t0023g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.48+4578C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429613 | |||||||
chr12:51429668 | A | C | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+4633A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429668 | |||||||
chr12:51429705 | C | T | 1 | a0001c0002t0005g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.48+4670C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429705 | |||||||
chr12:51429709 | A | G | 49 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(46): Show |
49 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.48+4674A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51429709 | |||||||
chr12:51430133 | A | G | 1 | a0001c0008t0036g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48+5098A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430133 | |||||||
chr12:51430232 | T | C | 28 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(25): Show |
28 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.48+5197T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430232 | |||||||
chr12:51430362 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.48+5327G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430362 | |||||||
chr12:51430524 | G | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+5489G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430524 | |||||||
chr12:51430583 | A | G | 302 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.48+5548A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430583 | |||||||
chr12:51430640 | C | T | 302 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.48+5605C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430640 | |||||||
chr12:51430643 | G | C | 1 | a0001c0001t0048g0027 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.48+5608G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430643 | |||||||
chr12:51430653 | G | A | 302 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.48+5618G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430653 | |||||||
chr12:51430670 | C | A | 1 | a0001c0001t0025g0028 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.48+5635C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51430670 | |||||||
chr12:51431082 | A | G | 1 | a0001c0003t0005g0008 | 2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.48+6047A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51431082 | |||||||
chr12:51431212 | C | T | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+6177C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51431212 | |||||||
chr12:51431604 | A | AT | 42 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0033 others(39): Show |
42 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.48+6579dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51431604 | ||||||
chr12:51431956 | T | A | 1 | a0001c0002t0005g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48+6921T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51431956 | |||||||
chr12:51432033 | T | A | 1 | a0001c0001t0001g0187 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.48+6998T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432033 | |||||||
chr12:51432137 | G | A | 1 | a0001c0001t0004g0033 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.48+7102G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432137 | |||||||
chr12:51432283 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.48+7248C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432283 | |||||||
chr12:51432294 | C | T | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+7259C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432294 | |||||||
chr12:51432303 | C | T | 1 | a0001c0001t0043g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.48+7268C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432303 | |||||||
chr12:51432410 | C | CA | 156 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0022 others(153): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.48+7393dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51432410 | ||||||
chr12:51432410 | C | CAA | 90 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(87): Show |
91 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.48+7392_48+7393dup others(2): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51432410 | ||||||
chr12:51432474 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.48+7439C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432474 | |||||||
chr12:51432535 | G | A | 5 | a0001c0001t0003g0014 a0001c0001t0003g0296 a0001c0001t0003g0298 others(2): Show |
6 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+7500G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432535 | |||||||
chr12:51432646 | C | T | 1 | a0001c0003t0005g0183 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.48+7611C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432646 | |||||||
chr12:51432719 | C | T | 1 | a0001c0001t0023g0149 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.48+7684C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432719 | |||||||
chr12:51432755 | C | A | 1 | a0003c0009t0013g0082 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.48+7720C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432755 | |||||||
chr12:51432764 | A | G | 1 | a0001c0001t0006g0148 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.48+7729A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432764 | |||||||
chr12:51432769 | T | C | 7 | a0001c0001t0006g0005 a0001c0001t0006g0016 a0001c0001t0006g0017 others(4): Show |
8 | HG02895.hp1 HG02922.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+7734T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432769 | |||||||
chr12:51432910 | T | C | 1 | a0001c0001t0003g0301 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.49-7798T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432910 | |||||||
chr12:51432938 | T | G | 1 | a0001c0001t0023g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.49-7770T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51432938 | |||||||
chr12:51433335 | C | T | 176 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(173): Show |
183 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.49-7373C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433335 | |||||||
chr12:51433559 | T | G | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-7149T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433559 | |||||||
chr12:51433771 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.49-6937G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433771 | |||||||
chr12:51433826 | G | T | 1 | a0001c0001t0021g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.49-6882G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433826 | |||||||
chr12:51433828 | C | G | 1 | a0001c0001t0021g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.49-6880C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433828 | |||||||
chr12:51433851 | G | GT | 31 | a0001c0001t0001g0185 a0001c0001t0001g0190 a0001c0001t0001g0192 others(28): Show |
31 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.49-6830dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51433851 | ||||||
chr12:51433851 | GT | G | 31 | a0001c0001t0001g0193 a0001c0001t0001g0245 a0001c0001t0001g0246 others(28): Show |
35 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.49-6830delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51433851 | ||||||
chr12:51433851 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0001g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.49-6839_49-6830del others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51433851 | ||||||
chr12:51433861 | T | G | 10 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(7): Show |
11 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.49-6847T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433861 | |||||||
chr12:51433862 | T | G | 142 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(139): Show |
148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.49-6846T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433862 | |||||||
chr12:51433866 | T | G | 62 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(59): Show |
67 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.49-6842T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433866 | |||||||
chr12:51433867 | T | G | 142 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(139): Show |
148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.49-6841T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433867 | |||||||
chr12:51433868 | TTTTTTTT others(5): Show |
T | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.49-6837_49-6826del others(12): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51433868 | ||||||
chr12:51433869 | TTTTTTTT others(4): Show |
T | 142 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(139): Show |
148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.49-6836_49-6826del others(11): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51433869 | ||||||
chr12:51433871 | T | G | 1 | a0001c0001t0003g0004 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.49-6837T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433871 | |||||||
chr12:51433875 | T | G | 17 | a0001c0001t0001g0022 a0001c0001t0001g0189 a0001c0001t0001g0246 others(14): Show |
17 | HG00597.hp1 HG00642.hp1 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.49-6833T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433875 | |||||||
chr12:51433875 | T | TG | 4 | a0001c0001t0001g0195 a0001c0001t0001g0221 a0001c0001t0001g0259 others(1): Show |
4 | HG00140.hp2 HG02109.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-6833_49-6832ins others(1): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433875 | |||||||
chr12:51433880 | G | T | 163 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(160): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.49-6828G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433880 | |||||||
chr12:51433887 | T | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0186 others(1): Show |
4 | HG00642.hp1 HG01993.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-6821T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433887 | |||||||
chr12:51433934 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.49-6774G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51433934 | |||||||
chr12:51434153 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG00140.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.49-6555G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51434153 | |||||||
chr12:51434331 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.49-6377G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51434331 | |||||||
chr12:51434481 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.49-6227A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51434481 | |||||||
chr12:51434516 | G | A | 6 | a0001c0001t0009g0076 a0001c0001t0009g0087 a0001c0001t0009g0089 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-6192G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51434516 | |||||||
chr12:51434814 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.49-5894C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51434814 | |||||||
chr12:51434845 | A | G | 1 | a0001c0001t0043g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.49-5863A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51434845 | |||||||
chr12:51435022 | G | C | 1 | a0001c0001t0004g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.49-5686G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435022 | |||||||
chr12:51435073 | A | T | 1 | a0001c0002t0010g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.49-5635A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435073 | |||||||
chr12:51435326 | T | C | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-5382T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435326 | |||||||
chr12:51435588 | C | T | 1 | a0001c0001t0003g0301 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.49-5120C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435588 | |||||||
chr12:51435589 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0291 |
3 | HG00733.hp1 HG00735.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.49-5119G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435589 | |||||||
chr12:51435678 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.49-5030A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435678 | |||||||
chr12:51435748 | G | C | 1 | a0001c0001t0002g0092 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.49-4960G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435748 | |||||||
chr12:51435762 | T | C | 1 | a0001c0001t0003g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.49-4946T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435762 | |||||||
chr12:51435863 | C | T | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-4845C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435863 | |||||||
chr12:51435877 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | NA18970.hp2 NA18981.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.49-4831C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51435877 | |||||||
chr12:51436026 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.49-4682A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51436026 | |||||||
chr12:51436037 | A | G | 9 | a0001c0001t0002g0146 a0001c0001t0009g0076 a0001c0001t0009g0087 others(6): Show |
9 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.49-4671A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51436037 | |||||||
chr12:51436115 | T | G | 1 | a0001c0001t0003g0302 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.49-4593T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51436115 | |||||||
chr12:51436321 | A | G | 28 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(25): Show |
28 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.49-4387A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51436321 | |||||||
chr12:51436493 | A | G | 1 | a0001c0001t0004g0064 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.49-4215A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51436493 | |||||||
chr12:51436606 | G | GTTAT | 6 | a0001c0001t0001g0225 a0001c0001t0001g0271 a0001c0001t0003g0323 others(3): Show |
6 | HG00597.hp1 HG02080.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-4086_49-4083dup others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51436606 | ||||||
chr12:51436622 | TTTAG | T | 6 | a0001c0001t0001g0225 a0001c0001t0001g0271 a0001c0001t0003g0323 others(3): Show |
6 | HG00597.hp1 HG02080.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-4070_49-4067del others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51436622 | ||||||
chr12:51436772 | G | A | 4 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(1): Show |
4 | HG02895.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-3936G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51436772 | |||||||
chr12:51437353 | A | G | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-3355A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51437353 | |||||||
chr12:51437438 | A | G | 28 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(25): Show |
28 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.49-3270A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51437438 | |||||||
chr12:51437475 | A | C | 2 | a0001c0002t0005g0176 a0001c0002t0005g0177 |
2 | NA18966.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.49-3233A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51437475 | |||||||
chr12:51437985 | A | T | 1 | a0001c0001t0040g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.49-2723A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51437985 | |||||||
chr12:51437987 | G | A | 123 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(120): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.49-2721G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51437987 | |||||||
chr12:51438055 | G | A | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.49-2653G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438055 | |||||||
chr12:51438203 | A | G | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(121): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.49-2505A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438203 | |||||||
chr12:51438312 | C | T | 1 | a0001c0001t0007g0224 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.49-2396C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438312 | |||||||
chr12:51438501 | T | A | 13 | a0001c0001t0002g0001 a0001c0001t0002g0086 a0001c0001t0002g0093 others(10): Show |
14 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.49-2207T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438501 | |||||||
chr12:51438676 | C | A | 1 | a0001c0001t0002g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.49-2032C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438676 | |||||||
chr12:51438720 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.49-1988C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438720 | |||||||
chr12:51438756 | G | C | 1 | a0001c0002t0005g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.49-1952G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438756 | |||||||
chr12:51438771 | A | G | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(121): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.49-1937A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438771 | |||||||
chr12:51438817 | A | T | 1 | a0001c0001t0006g0148 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.49-1891A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438817 | |||||||
chr12:51438907 | T | C | 1 | a0001c0001t0040g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.49-1801T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51438907 | |||||||
chr12:51438911 | CTATT | C | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.49-1795_49-1792del others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51438911 | ||||||
chr12:51439087 | C | T | 123 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(120): Show |
128 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.49-1621C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51439087 | |||||||
chr12:51439294 | T | G | 1 | a0001c0001t0023g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.49-1414T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51439294 | |||||||
chr12:51439311 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.49-1397C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51439311 | |||||||
chr12:51439611 | T | TA | 7 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0106 others(4): Show |
7 | HG00280.hp1 HG01255.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-1086dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51439611 | ||||||
chr12:51439969 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.49-739A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51439969 | |||||||
chr12:51440224 | G | A | 83 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(80): Show |
89 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.49-484G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51440224 | |||||||
chr12:51440279 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.49-429A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51440279 | |||||||
chr12:51440403 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.49-305T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51440403 | |||||||
chr12:51440410 | GT | G | 173 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(170): Show |
180 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.49-283delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr12 | 51440410 | ||||||
chr12:51440440 | C | T | 3 | a0001c0002t0027g0293 a0001c0002t0027g0294 a0001c0002t0044g0295 |
3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.49-268C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 1/24 | chr12 | 51440440 | |||||||
chr12:51441207 | C | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0242 |
2 | HG01975.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.130+418C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441207 | |||||||
chr12:51441400 | T | G | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | NA19066.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.130+611T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441400 | |||||||
chr12:51441476 | T | C | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.130+687T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441476 | |||||||
chr12:51441698 | A | G | 3 | a0001c0002t0005g0173 a0001c0002t0005g0175 a0001c0002t0045g0174 |
3 | NA18955.hp2 NA18988.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.130+909A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441698 | |||||||
chr12:51441715 | C | G | 1 | a0001c0001t0008g0282 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.130+926C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441715 | |||||||
chr12:51441793 | G | A | 48 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(45): Show |
48 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.130+1004G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441793 | |||||||
chr12:51441799 | G | A | 1 | a0001c0001t0037g0339 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.130+1010G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441799 | |||||||
chr12:51441958 | A | C | 28 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(25): Show |
28 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.130+1169A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51441958 | |||||||
chr12:51442476 | C | T | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.130+1687C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51442476 | |||||||
chr12:51442515 | G | A | 2 | a0001c0001t0002g0146 a0001c0001t0008g0249 |
2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.130+1726G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51442515 | |||||||
chr12:51442641 | G | A | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.130+1852G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51442641 | |||||||
chr12:51442832 | C | T | 180 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(177): Show |
187 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.130+2043C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51442832 | |||||||
chr12:51442839 | C | T | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.130+2050C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51442839 | |||||||
chr12:51443093 | A | G | 1 | a0001c0001t0002g0142 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.130+2304A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51443093 | |||||||
chr12:51443268 | C | T | 1 | a0001c0001t0040g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.130+2479C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51443268 | |||||||
chr12:51443275 | C | T | 2 | a0001c0001t0018g0270 a0001c0001t0018g0281 |
2 | NA18989.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.130+2486C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51443275 | |||||||
chr12:51443836 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.130+3047C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51443836 | |||||||
chr12:51443894 | A | G | 1 | a0001c0002t0005g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.130+3105A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51443894 | |||||||
chr12:51444005 | T | C | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.130+3216T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444005 | |||||||
chr12:51444030 | T | C | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+3241T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444030 | |||||||
chr12:51444359 | C | T | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.130+3570C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444359 | |||||||
chr12:51444422 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.130+3633A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444422 | |||||||
chr12:51444505 | A | G | 5 | a0001c0001t0001g0192 a0001c0001t0001g0222 a0001c0001t0001g0241 others(2): Show |
5 | HG00438.hp2 HG00621.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+3716A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444505 | |||||||
chr12:51444680 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130+3891G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444680 | |||||||
chr12:51444718 | T | C | 11 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0297 others(8): Show |
14 | HG00673.hp1 HG00735.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+3929T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444718 | |||||||
chr12:51444881 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.130+4092A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51444881 | |||||||
chr12:51445125 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.130+4336C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51445125 | |||||||
chr12:51445350 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.130+4561T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51445350 | |||||||
chr12:51445579 | C | T | 1 | a0001c0002t0005g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.130+4790C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51445579 | |||||||
chr12:51445620 | G | A | 4 | a0001c0001t0001g0246 a0001c0001t0001g0286 a0001c0001t0020g0324 others(1): Show |
4 | HG01346.hp1 HG02257.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+4831G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51445620 | |||||||
chr12:51445853 | AC | A | 176 | a0001c0001t0001g0247 a0001c0001t0002g0001 a0001c0001t0002g0002 others(173): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.131-5015delC | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51445853 | ||||||
chr12:51446019 | T | A | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | NA18979.hp1 NA19004.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.131-4857T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446019 | |||||||
chr12:51446036 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.131-4840A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446036 | |||||||
chr12:51446363 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.131-4513C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446363 | |||||||
chr12:51446547 | AAAG | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-4321_131-4319d others(5): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51446547 | ||||||
chr12:51446619 | C | T | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-4257C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446619 | |||||||
chr12:51446751 | T | C | 1 | a0001c0001t0001g0009 | 2 | NA18980.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.131-4125T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446751 | |||||||
chr12:51446906 | C | T | 1 | a0001c0001t0051g0062 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.131-3970C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446906 | |||||||
chr12:51446959 | G | C | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | NA18999.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.131-3917G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446959 | |||||||
chr12:51446969 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.131-3907A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51446969 | |||||||
chr12:51447036 | G | C | 1 | a0001c0001t0040g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.131-3840G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447036 | |||||||
chr12:51447048 | G | GTCTGTCT others(5): Show |
40 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0078 others(37): Show |
43 | HG00099.hp2 HG00544.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.131-3821_131-3820i others(14): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447048 | ||||||
chr12:51447052 | G | GTCTATCT others(1): Show |
46 | a0001c0001t0002g0001 a0001c0001t0002g0093 a0001c0001t0002g0095 others(43): Show |
47 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.131-3821_131-3820i others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447052 | ||||||
chr12:51447052 | G | GTCTATCT others(9): Show |
20 | a0001c0001t0002g0081 a0001c0001t0002g0105 a0001c0001t0002g0106 others(17): Show |
20 | HG00280.hp1 HG00741.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.131-3821_131-3820i others(18): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447052 | ||||||
chr12:51447052 | G | GTCTATCT others(13): Show |
15 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(12): Show |
15 | HG00639.hp1 HG01978.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.131-3821_131-3820i others(22): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447052 | ||||||
chr12:51447052 | G | GTCTATCT others(17): Show |
7 | a0001c0001t0002g0006 a0001c0001t0002g0109 a0001c0001t0002g0112 others(4): Show |
9 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.131-3821_131-3820i others(26): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447052 | ||||||
chr12:51447052 | G | GTCTATCT others(21): Show |
2 | a0001c0001t0002g0068 a0001c0001t0002g0069 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.131-3821_131-3820i others(30): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447052 | ||||||
chr12:51447056 | G | A | 95 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(92): Show |
100 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.131-3820G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447056 | |||||||
chr12:51447060 | A | ATCTG | 10 | a0001c0001t0004g0061 a0001c0001t0009g0076 a0001c0001t0009g0087 others(7): Show |
10 | HG02071.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-3813_131-3812i others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447060 | ||||||
chr12:51447064 | A | G | 1 | a0001c0001t0002g0291 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.131-3812A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447064 | |||||||
chr12:51447064 | ATCTG | A | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | NA18970.hp2 NA18981.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.131-3808_131-3805d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447064 | ||||||
chr12:51447068 | G | A | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.131-3808G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447068 | |||||||
chr12:51447068 | G | GTCTA | 20 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0261 others(17): Show |
21 | HG00558.hp1 HG00597.hp1 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.131-3787_131-3784d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447068 | ||||||
chr12:51447071 | T | G | 1 | a0001c0001t0004g0066 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.131-3805T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447071 | |||||||
chr12:51447099 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.131-3777G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447099 | |||||||
chr12:51447130 | G | A | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.131-3746G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447130 | |||||||
chr12:51447460 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.131-3416G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447460 | |||||||
chr12:51447479 | A | C | 1 | a0004c0012t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.131-3397A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447479 | |||||||
chr12:51447647 | G | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-3229G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447647 | |||||||
chr12:51447714 | C | CT | 33 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0002g0101 others(30): Show |
37 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.131-3142dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447714 | ||||||
chr12:51447714 | C | CTT | 43 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(40): Show |
43 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.131-3143_131-3142d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447714 | ||||||
chr12:51447714 | CT | C | 32 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0286 others(29): Show |
32 | HG00558.hp2 HG01346.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.131-3142delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51447714 | ||||||
chr12:51447774 | T | C | 2 | a0001c0001t0042g0150 a0001c0001t0043g0151 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.131-3102T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447774 | |||||||
chr12:51447877 | C | T | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.131-2999C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447877 | |||||||
chr12:51447909 | C | T | 5 | a0001c0001t0004g0025 a0001c0001t0004g0058 a0001c0001t0004g0060 others(2): Show |
5 | HG01099.hp2 HG01167.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-2967C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447909 | |||||||
chr12:51447966 | G | A | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-2910G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51447966 | |||||||
chr12:51448136 | T | C | 1 | a0001c0001t0037g0339 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.131-2740T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448136 | |||||||
chr12:51448189 | A | C | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.131-2687A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448189 | |||||||
chr12:51448385 | A | G | 1 | a0001c0001t0004g0067 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.131-2491A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448385 | |||||||
chr12:51448724 | G | C | 1 | a0001c0001t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.131-2152G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448724 | |||||||
chr12:51448758 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.131-2118A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448758 | |||||||
chr12:51448816 | C | T | 1 | a0001c0001t0023g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.131-2060C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448816 | |||||||
chr12:51448966 | G | A | 1 | a0001c0001t0023g0149 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131-1910G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51448966 | |||||||
chr12:51449281 | C | CA | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-1588dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51449281 | ||||||
chr12:51449324 | G | T | 1 | a0001c0002t0005g0171 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.131-1552G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51449324 | |||||||
chr12:51449435 | G | GA | 125 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(122): Show |
130 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.131-1428dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 51449435 | ||||||
chr12:51449534 | C | T | 28 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(25): Show |
28 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.131-1342C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51449534 | |||||||
chr12:51449578 | T | A | 1 | a0001c0001t0007g0252 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.131-1298T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51449578 | |||||||
chr12:51449702 | G | A | 1 | a0001c0001t0025g0028 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.131-1174G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51449702 | |||||||
chr12:51449799 | C | T | 1 | a0001c0001t0004g0042 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.131-1077C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51449799 | |||||||
chr12:51449854 | C | T | 8 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0106 others(5): Show |
8 | HG00280.hp1 HG01169.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-1022C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51449854 | |||||||
chr12:51450067 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0286 |
2 | HG01346.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.131-809A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51450067 | |||||||
chr12:51450470 | G | A | 3 | a0001c0001t0003g0302 a0001c0001t0003g0313 a0001c0001t0003g0329 |
3 | HG00609.hp2 NA18971.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.131-406G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51450470 | |||||||
chr12:51450715 | A | G | 21 | a0001c0001t0002g0001 a0001c0001t0002g0093 a0001c0001t0002g0095 others(18): Show |
22 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.131-161A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51450715 | |||||||
chr12:51450831 | T | A | 1 | a0001c0001t0026g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.131-45T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 2/24 | chr12 | 51450831 | |||||||
chr12:51451123 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.277+101C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451123 | |||||||
chr12:51451164 | G | T | 3 | a0001c0001t0002g0146 a0001c0001t0023g0149 a0001c0001t0040g0147 |
3 | HG02559.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.277+142G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451164 | |||||||
chr12:51451274 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.277+252G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451274 | |||||||
chr12:51451383 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.277+361G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451383 | |||||||
chr12:51451429 | T | A | 1 | a0001c0001t0001g0273 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.277+407T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451429 | |||||||
chr12:51451584 | C | G | 1 | a0001c0002t0005g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.278-540C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451584 | |||||||
chr12:51451633 | A | C | 1 | a0001c0001t0002g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.278-491A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451633 | |||||||
chr12:51451666 | G | T | 1 | a0001c0001t0037g0339 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.278-458G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451666 | |||||||
chr12:51451911 | C | T | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.278-213C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451911 | |||||||
chr12:51451918 | T | G | 1 | a0001c0002t0010g0024 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.278-206T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51451918 | |||||||
chr12:51452020 | G | A | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-104G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51452020 | |||||||
chr12:51452023 | G | A | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-101G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 3/24 | chr12 | 51452023 | |||||||
chr12:51452306 | G | A | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.413+47G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452306 | |||||||
chr12:51452346 | T | A | 1 | a0001c0001t0001g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.413+87T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452346 | |||||||
chr12:51452371 | A | G | 1 | a0001c0002t0005g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.413+112A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452371 | |||||||
chr12:51452448 | A | G | 3 | a0001c0001t0021g0157 a0001c0001t0022g0155 a0001c0001t0022g0156 |
3 | HG02055.hp2 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.413+189A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452448 | |||||||
chr12:51452477 | T | C | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.413+218T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452477 | |||||||
chr12:51452491 | A | G | 1 | a0001c0001t0001g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.413+232A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452491 | |||||||
chr12:51452653 | C | G | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+394C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452653 | |||||||
chr12:51452659 | G | C | 4 | a0001c0001t0002g0001 a0001c0001t0002g0093 a0001c0001t0002g0095 others(1): Show |
5 | HG00642.hp2 HG01496.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+400G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452659 | |||||||
chr12:51452758 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.413+499G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452758 | |||||||
chr12:51452768 | T | A | 1 | a0001c0001t0002g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.413+509T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452768 | |||||||
chr12:51452768 | T | G | 174 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(171): Show |
181 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.413+509T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51452768 | |||||||
chr12:51453128 | T | A | 1 | a0001c0001t0001g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-411T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51453128 | |||||||
chr12:51453134 | G | A | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.414-405G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51453134 | |||||||
chr12:51453160 | C | A | 2 | a0001c0001t0002g0070 a0001c0001t0002g0072 |
2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.414-379C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 4/24 | chr12 | 51453160 | |||||||
chr12:51453776 | C | A | 1 | a0001c0001t0037g0339 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.574+77C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51453776 | |||||||
chr12:51453870 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0221 a0001c0001t0001g0239 |
3 | HG00140.hp2 HG01358.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.574+171C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51453870 | |||||||
chr12:51453924 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.574+225T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51453924 | |||||||
chr12:51454016 | C | T | 32 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0188 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.574+317C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454016 | |||||||
chr12:51454061 | C | G | 7 | a0001c0001t0004g0026 a0001c0001t0004g0033 a0001c0001t0004g0034 others(4): Show |
7 | HG02027.hp2 HG02040.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.574+362C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454061 | |||||||
chr12:51454220 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.574+521C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454220 | |||||||
chr12:51454268 | G | A | 8 | a0001c0001t0009g0076 a0001c0001t0009g0087 a0001c0001t0009g0089 others(5): Show |
8 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.574+569G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454268 | |||||||
chr12:51454422 | T | G | 1 | a0001c0001t0002g0103 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.574+723T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454422 | |||||||
chr12:51454429 | G | T | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.574+730G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454429 | |||||||
chr12:51454643 | T | A | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.574+944T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454643 | |||||||
chr12:51454837 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.574+1138C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454837 | |||||||
chr12:51454845 | G | A | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(121): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.574+1146G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454845 | |||||||
chr12:51454874 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.574+1175C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51454874 | |||||||
chr12:51455061 | C | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.574+1362C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455061 | |||||||
chr12:51455117 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.574+1418G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455117 | |||||||
chr12:51455170 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.574+1471A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455170 | |||||||
chr12:51455271 | TA | T | 7 | a0001c0001t0001g0245 a0001c0001t0001g0268 a0001c0001t0003g0321 others(4): Show |
7 | HG01074.hp2 HG01515.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.574+1587delA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 51455271 | ||||||
chr12:51455324 | G | A | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.574+1625G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455324 | |||||||
chr12:51455522 | A | G | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.574+1823A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455522 | |||||||
chr12:51455640 | G | A | 83 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(80): Show |
89 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.575-1711G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455640 | |||||||
chr12:51455687 | C | T | 1 | a0001c0002t0005g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.575-1664C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455687 | |||||||
chr12:51455809 | C | T | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-1542C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455809 | |||||||
chr12:51455983 | C | T | 1 | a0001c0006t0002g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.575-1368C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51455983 | |||||||
chr12:51456026 | A | G | 1 | a0001c0001t0003g0329 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.575-1325A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456026 | |||||||
chr12:51456189 | TGATA | T | 50 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(47): Show |
55 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.575-1155_575-1152d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 51456189 | ||||||
chr12:51456244 | G | A | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.575-1107G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456244 | |||||||
chr12:51456647 | A | AAGATCAC others(27): Show |
1 | a0001c0001t0001g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.575-696_575-695ins others(34): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 51456647 | ||||||
chr12:51456694 | T | C | 1 | a0001c0001t0001g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.575-657T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456694 | |||||||
chr12:51456833 | G | A | 2 | a0001c0001t0020g0324 a0001c0001t0020g0325 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.575-518G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456833 | |||||||
chr12:51456900 | T | A | 2 | a0001c0001t0042g0150 a0001c0001t0043g0151 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.575-451T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456900 | |||||||
chr12:51456943 | A | G | 177 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0002g0001 others(174): Show |
184 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.575-408A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456943 | |||||||
chr12:51456956 | A | T | 1 | a0001c0001t0001g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.575-395A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51456956 | |||||||
chr12:51457064 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.575-287T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51457064 | |||||||
chr12:51457094 | T | C | 4 | a0001c0001t0002g0001 a0001c0001t0002g0093 a0001c0001t0002g0095 others(1): Show |
5 | HG00642.hp2 HG01496.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.575-257T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51457094 | |||||||
chr12:51457180 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.575-171G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51457180 | |||||||
chr12:51457342 | G | A | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.575-9G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 5/24 | chr12 | 51457342 | |||||||
chr12:51457786 | G | A | 1 | a0001c0001t0002g0007 | 2 | NA18952.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.763+247G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 6/24 | chr12 | 51457786 | |||||||
chr12:51457836 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.763+297C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 6/24 | chr12 | 51457836 | |||||||
chr12:51458366 | A | C | 1 | a0001c0001t0032g0292 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.764-193A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 6/24 | chr12 | 51458366 | |||||||
chr12:51458676 | T | C | 1 | a0001c0001t0001g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.855+26T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51458676 | |||||||
chr12:51458727 | C | T | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.855+77C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51458727 | |||||||
chr12:51458949 | G | GCTCTCCA others(10): Show |
1 | a0001c0014t0003g0320 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.855+303_855+319dup others(17): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr12 | 51458949 | ||||||
chr12:51458977 | G | A | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.855+327G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51458977 | |||||||
chr12:51459036 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.855+386A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459036 | |||||||
chr12:51459260 | C | T | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.855+610C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459260 | |||||||
chr12:51459315 | A | G | 1 | a0001c0008t0036g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.856-636A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459315 | |||||||
chr12:51459340 | G | A | 1 | a0001c0001t0033g0253 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.856-611G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459340 | |||||||
chr12:51459408 | C | T | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.856-543C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459408 | |||||||
chr12:51459440 | A | G | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.856-511A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459440 | |||||||
chr12:51459739 | G | A | 2 | a0001c0001t0004g0043 a0001c0001t0026g0036 |
2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.856-212G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 7/24 | chr12 | 51459739 | |||||||
chr12:51460142 | C | T | 26 | a0001c0001t0001g0013 a0001c0001t0001g0185 a0001c0001t0001g0238 others(23): Show |
27 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.1013+34C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51460142 | |||||||
chr12:51460173 | G | A | 1 | a0004c0012t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1013+65G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51460173 | |||||||
chr12:51460391 | CT | C | 303 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(300): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1013+289delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 51460391 | ||||||
chr12:51460719 | C | T | 1 | a0001c0002t0044g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1014-485C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51460719 | |||||||
chr12:51460720 | G | A | 1 | a0001c0001t0023g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1014-484G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51460720 | |||||||
chr12:51460794 | T | C | 8 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0106 others(5): Show |
8 | HG00280.hp1 HG01169.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1014-410T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51460794 | |||||||
chr12:51461046 | C | G | 1 | a0001c0006t0002g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1014-158C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51461046 | |||||||
chr12:51461074 | T | C | 1 | a0001c0001t0001g0284 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1014-130T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51461074 | |||||||
chr12:51461105 | A | G | 1 | a0001c0001t0015g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1014-99A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51461105 | |||||||
chr12:51461111 | G | T | 1 | a0001c0001t0002g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1014-93G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51461111 | |||||||
chr12:51461113 | T | C | 1 | a0001c0001t0004g0032 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1014-91T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 8/24 | chr12 | 51461113 | |||||||
chr12:51461302 | C | G | 1 | a0001c0001t0004g0041 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1101+11C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51461302 | |||||||
chr12:51461476 | C | T | 1 | a0001c0001t0003g0302 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1101+185C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51461476 | |||||||
chr12:51461631 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1101+340A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51461631 | |||||||
chr12:51461719 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1101+428T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51461719 | |||||||
chr12:51461846 | C | T | 3 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 |
3 | HG01884.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1102-464C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51461846 | |||||||
chr12:51461884 | TTTGA | T | 43 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0032 others(40): Show |
43 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.1102-421_1102-418d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr12 | 51461884 | ||||||
chr12:51461943 | A | G | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1102-367A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51461943 | |||||||
chr12:51461990 | T | TA | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.1102-316dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr12 | 51461990 | ||||||
chr12:51462072 | T | G | 2 | a0001c0001t0020g0324 a0001c0001t0020g0325 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1102-238T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51462072 | |||||||
chr12:51462144 | A | C | 1 | a0001c0001t0048g0027 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1102-166A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51462144 | |||||||
chr12:51462200 | G | A | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.1102-110G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 9/24 | chr12 | 51462200 | |||||||
chr12:51462486 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1248+30A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51462486 | |||||||
chr12:51462538 | A | G | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248+82A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51462538 | |||||||
chr12:51462695 | C | A | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1248+239C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51462695 | |||||||
chr12:51462807 | C | T | 1 | a0001c0001t0023g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1248+351C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51462807 | |||||||
chr12:51462851 | T | C | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.1248+395T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51462851 | |||||||
chr12:51462892 | C | CA | 10 | a0001c0001t0001g0189 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
10 | HG01891.hp1 HG02080.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1248+453dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51462892 | ||||||
chr12:51462892 | C | CAA | 166 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(163): Show |
173 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.1248+452_1248+453d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51462892 | ||||||
chr12:51462966 | G | A | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248+510G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51462966 | |||||||
chr12:51463042 | T | C | 1 | a0001c0008t0036g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1249-572T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463042 | |||||||
chr12:51463076 | G | A | 83 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(80): Show |
89 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1249-538G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463076 | |||||||
chr12:51463110 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1249-504T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463110 | |||||||
chr12:51463409 | G | C | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1249-205G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463409 | |||||||
chr12:51463410 | G | GGT | 35 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0001g0277 others(32): Show |
40 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1249-165_1249-164d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51463410 | ||||||
chr12:51463410 | G | GGTGT | 12 | a0001c0001t0001g0213 a0001c0001t0001g0246 a0001c0001t0001g0260 others(9): Show |
13 | HG01433.hp1 HG01515.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1249-167_1249-164d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51463410 | ||||||
chr12:51463410 | GGT | G | 56 | a0001c0001t0001g0194 a0001c0001t0001g0240 a0001c0001t0001g0258 others(53): Show |
57 | HG00438.hp1 HG00673.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1249-165_1249-164d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51463410 | ||||||
chr12:51463410 | GGTGT | G | 102 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(99): Show |
109 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1249-167_1249-164d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51463410 | ||||||
chr12:51463410 | GGTGTGT | G | 7 | a0001c0001t0002g0136 a0001c0001t0004g0025 a0001c0001t0004g0058 others(4): Show |
7 | HG01099.hp2 HG01167.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1249-169_1249-164d others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51463410 | ||||||
chr12:51463410 | GGTGTGTG others(5): Show |
G | 1 | a0001c0001t0003g0319 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1249-175_1249-164d others(14): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 51463410 | ||||||
chr12:51463412 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1249-202T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463412 | |||||||
chr12:51463480 | C | T | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1249-134C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463480 | |||||||
chr12:51463577 | T | A | 1 | a0001c0001t0049g0045 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1249-37T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 10/24 | chr12 | 51463577 | |||||||
chr12:51463805 | C | T | 2 | a0001c0001t0042g0150 a0001c0001t0043g0151 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1349+91C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51463805 | |||||||
chr12:51464064 | C | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1349+350C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51464064 | |||||||
chr12:51464117 | AC | A | 178 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0002g0001 others(175): Show |
185 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.1349+406delC | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 51464117 | ||||||
chr12:51464214 | G | T | 1 | a0001c0001t0001g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1349+500G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51464214 | |||||||
chr12:51464530 | T | G | 1 | a0001c0008t0036g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1349+816T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51464530 | |||||||
chr12:51464573 | G | A | 1 | a0001c0001t0004g0064 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1349+859G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51464573 | |||||||
chr12:51464793 | G | A | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1349+1079G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51464793 | |||||||
chr12:51464835 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1349+1121A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51464835 | |||||||
chr12:51465057 | T | C | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(121): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1349+1343T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465057 | |||||||
chr12:51465513 | G | T | 1 | a0001c0002t0010g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1349+1799G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465513 | |||||||
chr12:51465524 | T | C | 2 | a0001c0001t0020g0324 a0001c0001t0020g0325 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1349+1810T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465524 | |||||||
chr12:51465534 | C | G | 1 | a0001c0002t0005g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1349+1820C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465534 | |||||||
chr12:51465539 | C | T | 1 | a0001c0002t0005g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1349+1825C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465539 | |||||||
chr12:51465825 | C | A | 1 | a0001c0001t0008g0249 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1349+2111C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465825 | |||||||
chr12:51465910 | C | T | 1 | a0001c0001t0004g0042 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1349+2196C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51465910 | |||||||
chr12:51466059 | T | G | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(121): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1349+2345T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466059 | |||||||
chr12:51466166 | G | T | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1349+2452G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466166 | |||||||
chr12:51466240 | C | T | 1 | a0001c0001t0002g0007 | 2 | NA18952.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1349+2526C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466240 | |||||||
chr12:51466535 | CTTAAA | C | 83 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(80): Show |
89 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1349+2827_1349+283 others(9): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 51466535 | ||||||
chr12:51466595 | A | C | 1 | a0001c0002t0005g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1349+2881A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466595 | |||||||
chr12:51466695 | A | T | 46 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(43): Show |
46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1350-2919A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466695 | |||||||
chr12:51466729 | A | G | 1 | a0001c0001t0025g0028 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1350-2885A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466729 | |||||||
chr12:51466806 | A | T | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1350-2808A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51466806 | |||||||
chr12:51466943 | ATG | A | 296 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(293): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1350-2647_1350-264 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 51466943 | ||||||
chr12:51467070 | C | T | 2 | a0001c0002t0005g0168 a0001c0011t0047g0169 |
2 | NA18979.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1350-2544C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51467070 | |||||||
chr12:51467079 | A | C | 1 | a0001c0001t0003g0327 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1350-2535A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51467079 | |||||||
chr12:51467638 | T | G | 4 | a0001c0001t0002g0112 a0001c0001t0002g0116 a0001c0001t0002g0117 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350-1976T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51467638 | |||||||
chr12:51467666 | A | G | 6 | a0001c0001t0002g0006 a0001c0001t0002g0078 a0001c0001t0002g0092 others(3): Show |
7 | HG00733.hp1 HG00735.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1350-1948A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51467666 | |||||||
chr12:51467771 | CTTAAT | C | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350-1840_1350-183 others(9): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 51467771 | ||||||
chr12:51467864 | A | C | 1 | a0001c0001t0002g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1350-1750A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51467864 | |||||||
chr12:51468302 | T | A | 1 | a0001c0001t0001g0272 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1350-1312T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468302 | |||||||
chr12:51468321 | C | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0185 a0001c0001t0001g0238 others(3): Show |
7 | HG01081.hp2 HG01255.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1350-1293C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468321 | |||||||
chr12:51468333 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1350-1281C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468333 | |||||||
chr12:51468425 | C | G | 3 | a0001c0002t0027g0293 a0001c0002t0027g0294 a0001c0002t0044g0295 |
3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1350-1189C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468425 | |||||||
chr12:51468530 | C | T | 1 | a0001c0008t0036g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1350-1084C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468530 | |||||||
chr12:51468539 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1350-1075C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468539 | |||||||
chr12:51468754 | C | T | 1 | a0001c0001t0004g0051 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1350-860C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468754 | |||||||
chr12:51468865 | C | G | 4 | a0001c0001t0002g0112 a0001c0001t0002g0116 a0001c0001t0002g0117 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350-749C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468865 | |||||||
chr12:51468874 | C | G | 4 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(1): Show |
4 | HG02055.hp2 HG02809.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350-740C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468874 | |||||||
chr12:51468876 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1350-738C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51468876 | |||||||
chr12:51469174 | C | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1350-440C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51469174 | |||||||
chr12:51469544 | A | G | 8 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0106 others(5): Show |
8 | HG00280.hp1 HG01169.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1350-70A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51469544 | |||||||
chr12:51469553 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1350-61T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 11/24 | chr12 | 51469553 | |||||||
chr12:51469859 | T | C | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1524+71T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 12/24 | chr12 | 51469859 | |||||||
chr12:51470680 | C | T | 2 | a0001c0001t0020g0324 a0001c0001t0020g0325 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1658+155C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51470680 | |||||||
chr12:51470848 | C | T | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1658+323C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51470848 | |||||||
chr12:51470864 | T | G | 1 | a0001c0001t0001g0288 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1658+339T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51470864 | |||||||
chr12:51470874 | G | T | 1 | a0001c0001t0002g0081 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1658+349G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51470874 | |||||||
chr12:51470879 | G | GT | 85 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(82): Show |
91 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1658+361dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 51470879 | ||||||
chr12:51470957 | T | C | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1659-330T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51470957 | |||||||
chr12:51471098 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1659-189G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51471098 | |||||||
chr12:51471153 | G | C | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1659-134G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51471153 | |||||||
chr12:51471184 | G | A | 5 | a0001c0001t0003g0014 a0001c0001t0003g0296 a0001c0001t0003g0298 others(2): Show |
6 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1659-103G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51471184 | |||||||
chr12:51471195 | T | C | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.1659-92T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51471195 | |||||||
chr12:51471255 | A | G | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1659-32A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51471255 | |||||||
chr12:51471259 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1659-28G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 13/24 | chr12 | 51471259 | |||||||
chr12:51471651 | A | G | 1 | a0001c0001t0003g0311 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1904+119A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51471651 | |||||||
chr12:51471831 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1904+299A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51471831 | |||||||
chr12:51472038 | A | G | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1904+506A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472038 | |||||||
chr12:51472076 | C | T | 4 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(1): Show |
4 | HG02055.hp2 HG02809.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1904+544C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472076 | |||||||
chr12:51472169 | C | T | 3 | a0001c0002t0027g0293 a0001c0002t0027g0294 a0001c0002t0044g0295 |
3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1904+637C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472169 | |||||||
chr12:51472319 | C | T | 6 | a0001c0001t0002g0006 a0001c0001t0002g0078 a0001c0001t0002g0092 others(3): Show |
7 | HG00733.hp1 HG00735.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1904+787C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472319 | |||||||
chr12:51472361 | A | T | 1 | a0001c0001t0004g0050 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1904+829A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472361 | |||||||
chr12:51472605 | A | G | 1 | a0001c0001t0003g0300 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1904+1073A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472605 | |||||||
chr12:51472621 | C | T | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.1904+1089C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472621 | |||||||
chr12:51472622 | A | G | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.1904+1090A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472622 | |||||||
chr12:51472640 | G | A | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.1904+1108G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472640 | |||||||
chr12:51472880 | A | T | 1 | a0001c0003t0005g0008 | 2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1904+1348A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472880 | |||||||
chr12:51472911 | T | A | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1904+1379T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472911 | |||||||
chr12:51472977 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1905-1365C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472977 | |||||||
chr12:51472991 | A | G | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1905-1351A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51472991 | |||||||
chr12:51473050 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1905-1292C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51473050 | |||||||
chr12:51473114 | GATTTTGA others(19): Show |
G | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1905-1225_1905-120 others(30): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr12 | 51473114 | ||||||
chr12:51473158 | C | T | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | NA18999.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1905-1184C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51473158 | |||||||
chr12:51473275 | A | G | 1 | a0001c0002t0010g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1905-1067A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51473275 | |||||||
chr12:51473329 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1905-1013C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51473329 | |||||||
chr12:51473700 | A | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0286 |
2 | HG01346.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1905-642A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51473700 | |||||||
chr12:51473852 | A | G | 1 | a0001c0001t0014g0104 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1905-490A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51473852 | |||||||
chr12:51474027 | A | AAAAC | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1905-312_1905-311i others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr12 | 51474027 | ||||||
chr12:51474327 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1905-15A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 14/24 | chr12 | 51474327 | |||||||
chr12:51475237 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2172+31G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51475237 | |||||||
chr12:51475314 | G | A | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.2172+108G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51475314 | |||||||
chr12:51475618 | G | A | 1 | a0001c0001t0035g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2172+412G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51475618 | |||||||
chr12:51475748 | T | C | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2172+542T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51475748 | |||||||
chr12:51476070 | C | T | 1 | a0001c0002t0005g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2172+864C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476070 | |||||||
chr12:51476164 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2172+958A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476164 | |||||||
chr12:51476202 | C | T | 3 | a0001c0002t0027g0293 a0001c0002t0027g0294 a0001c0002t0044g0295 |
3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2172+996C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476202 | |||||||
chr12:51476231 | C | T | 3 | a0001c0002t0027g0293 a0001c0002t0027g0294 a0001c0002t0044g0295 |
3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2172+1025C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476231 | |||||||
chr12:51476459 | C | T | 1 | a0006c0015t0001g0331 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2172+1253C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476459 | |||||||
chr12:51476490 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2172+1284A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476490 | |||||||
chr12:51476536 | A | G | 2 | a0001c0001t0014g0020 a0001c0001t0014g0021 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2172+1330A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476536 | |||||||
chr12:51476602 | G | T | 8 | a0001c0001t0002g0006 a0001c0001t0002g0078 a0001c0001t0002g0092 others(5): Show |
9 | HG00733.hp1 HG00735.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.2172+1396G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476602 | |||||||
chr12:51476640 | G | A | 1 | a0001c0001t0016g0046 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2172+1434G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51476640 | |||||||
chr12:51476901 | CTTTTCTT others(4): Show |
C | 1 | a0001c0001t0001g0267 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2172+1700_2172+171 others(15): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51476901 | ||||||
chr12:51476906 | CT | C | 140 | a0001c0001t0001g0193 a0001c0001t0002g0001 a0001c0001t0002g0002 others(137): Show |
146 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.2172+1717delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51476906 | ||||||
chr12:51477001 | G | A | 21 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(18): Show |
21 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.2172+1795G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477001 | |||||||
chr12:51477345 | G | C | 1 | a0001c0001t0002g0103 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2172+2139G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477345 | |||||||
chr12:51477348 | T | TGGTATTA others(4): Show |
1 | a0001c0001t0017g0266 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2172+2143_2172+215 others(15): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51477348 | ||||||
chr12:51477578 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2172+2372C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477578 | |||||||
chr12:51477665 | T | A | 1 | a0002c0007t0003g0304 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2172+2459T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477665 | |||||||
chr12:51477788 | C | T | 5 | a0001c0001t0001g0200 a0001c0001t0001g0220 a0001c0001t0001g0230 others(2): Show |
5 | HG00099.hp1 HG01433.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.2172+2582C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477788 | |||||||
chr12:51477845 | A | G | 180 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(177): Show |
187 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.2172+2639A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477845 | |||||||
chr12:51477851 | A | G | 1 | a0001c0002t0005g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2172+2645A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477851 | |||||||
chr12:51477913 | C | T | 1 | a0001c0001t0023g0149 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2172+2707C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477913 | |||||||
chr12:51477914 | G | A | 1 | a0001c0001t0023g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2172+2708G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51477914 | |||||||
chr12:51478071 | C | T | 3 | a0001c0002t0027g0293 a0001c0002t0027g0294 a0001c0002t0044g0295 |
3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2172+2865C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478071 | |||||||
chr12:51478098 | AC | A | 4 | a0001c0003t0005g0008 a0001c0003t0005g0182 a0001c0003t0005g0183 others(1): Show |
5 | HG02572.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2172+2895delC | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51478098 | ||||||
chr12:51478154 | A | G | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.2172+2948A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478154 | |||||||
chr12:51478274 | C | CA | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
148 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.2172+3083dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51478274 | ||||||
chr12:51478274 | C | CAA | 31 | a0001c0001t0002g0093 a0001c0001t0002g0127 a0001c0001t0004g0061 others(28): Show |
31 | HG00558.hp2 HG01258.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.2172+3082_2172+308 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51478274 | ||||||
chr12:51478438 | T | TA | 12 | a0001c0001t0001g0283 a0001c0001t0021g0157 a0001c0001t0021g0158 others(9): Show |
13 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2172+3244dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51478438 | ||||||
chr12:51478453 | A | T | 180 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(177): Show |
187 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.2172+3247A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478453 | |||||||
chr12:51478492 | A | G | 175 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(172): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.2172+3286A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478492 | |||||||
chr12:51478517 | G | T | 5 | a0001c0001t0001g0193 a0001c0001t0001g0202 a0001c0001t0001g0207 others(2): Show |
5 | NA18988.hp1 NA19003.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.2172+3311G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478517 | |||||||
chr12:51478646 | C | T | 180 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(177): Show |
187 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.2172+3440C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478646 | |||||||
chr12:51478761 | C | T | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(121): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.2172+3555C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478761 | |||||||
chr12:51478795 | A | G | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.2172+3589A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51478795 | |||||||
chr12:51478939 | G | GCCTCA | 305 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(302): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2172+3734_2172+373 others(9): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51478939 | ||||||
chr12:51479103 | T | C | 1 | a0001c0001t0035g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2172+3897T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479103 | |||||||
chr12:51479325 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2172+4119T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479325 | |||||||
chr12:51479374 | T | C | 1 | a0001c0002t0005g0176 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2172+4168T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479374 | |||||||
chr12:51479410 | T | G | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2172+4204T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479410 | |||||||
chr12:51479441 | C | G | 1 | a0001c0001t0001g0276 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2172+4235C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479441 | |||||||
chr12:51479512 | C | T | 1 | a0001c0001t0016g0338 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2172+4306C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479512 | |||||||
chr12:51479530 | T | TA | 3 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 |
3 | HG01884.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2172+4325dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51479530 | ||||||
chr12:51479698 | AAG | A | 129 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(126): Show |
134 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.2172+4494_2172+449 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51479698 | ||||||
chr12:51479699 | AG | A | 46 | a0001c0001t0002g0006 a0001c0001t0002g0070 a0001c0001t0004g0038 others(43): Show |
47 | HG00558.hp2 HG00735.hp2 HG01261.hp2 others(44): Show |
intron_variant | MODIFIER | c.2172+4494delG | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479699 | |||||||
chr12:51479700 | G | A | 3 | a0001c0001t0021g0158 a0001c0001t0037g0339 a0001c0002t0010g0024 |
3 | HG01884.hp1 HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2172+4494G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479700 | |||||||
chr12:51479784 | A | G | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2172+4578A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479784 | |||||||
chr12:51479822 | T | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2172+4616T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51479822 | |||||||
chr12:51479969 | AT | A | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(155): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.2172+4782delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51479969 | ||||||
chr12:51479969 | ATT | A | 137 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(134): Show |
143 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.2172+4781_2172+478 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51479969 | ||||||
chr12:51480066 | G | A | 2 | a0001c0001t0024g0128 a0001c0001t0024g0137 |
2 | NA18981.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2172+4860G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480066 | |||||||
chr12:51480071 | G | A | 1 | a0001c0001t0023g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2172+4865G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480071 | |||||||
chr12:51480122 | G | A | 1 | a0001c0001t0040g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2172+4916G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480122 | |||||||
chr12:51480130 | G | A | 3 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 |
3 | HG01884.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2172+4924G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480130 | |||||||
chr12:51480190 | C | T | 1 | a0001c0001t0025g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2172+4984C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480190 | |||||||
chr12:51480270 | C | T | 57 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(54): Show |
61 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2172+5064C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480270 | |||||||
chr12:51480276 | C | A | 1 | a0001c0001t0001g0273 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2172+5070C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480276 | |||||||
chr12:51480326 | T | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0211 |
2 | NA18946.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2172+5120T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480326 | |||||||
chr12:51480369 | G | A | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2172+5163G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480369 | |||||||
chr12:51480372 | G | T | 68 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0022 others(65): Show |
72 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2172+5166G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480372 | |||||||
chr12:51480395 | G | A | 6 | a0001c0001t0009g0076 a0001c0001t0009g0087 a0001c0001t0009g0089 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2172+5189G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480395 | |||||||
chr12:51480431 | G | A | 1 | a0001c0002t0010g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2172+5225G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480431 | |||||||
chr12:51480612 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2173-5175G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480612 | |||||||
chr12:51480889 | G | A | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.2173-4898G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480889 | |||||||
chr12:51480890 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2173-4897C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51480890 | |||||||
chr12:51481341 | C | T | 1 | a0001c0001t0003g0323 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2173-4446C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481341 | |||||||
chr12:51481463 | G | A | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2173-4324G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481463 | |||||||
chr12:51481484 | A | G | 1 | a0001c0002t0005g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2173-4303A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481484 | |||||||
chr12:51481506 | C | G | 1 | a0001c0008t0036g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2173-4281C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481506 | |||||||
chr12:51481512 | G | A | 2 | a0001c0001t0042g0150 a0001c0001t0043g0151 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2173-4275G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481512 | |||||||
chr12:51481620 | T | C | 1 | a0001c0001t0026g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2173-4167T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481620 | |||||||
chr12:51481654 | G | C | 1 | a0001c0001t0001g0261 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2173-4133G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481654 | |||||||
chr12:51481722 | C | T | 1 | a0001c0001t0023g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2173-4065C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481722 | |||||||
chr12:51481729 | G | A | 141 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(138): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.2173-4058G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481729 | |||||||
chr12:51481790 | T | TA | 8 | a0001c0001t0001g0204 a0001c0001t0009g0076 a0001c0001t0009g0087 others(5): Show |
8 | HG02572.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2173-3985dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51481790 | ||||||
chr12:51481792 | A | T | 1 | a0001c0001t0003g0311 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2173-3995A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481792 | |||||||
chr12:51481815 | G | A | 1 | a0001c0008t0036g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2173-3972G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481815 | |||||||
chr12:51481916 | C | T | 304 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(301): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2173-3871C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51481916 | |||||||
chr12:51482091 | A | G | 1 | a0001c0001t0016g0337 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2173-3696A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482091 | |||||||
chr12:51482185 | C | G | 1 | a0001c0001t0003g0327 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2173-3602C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482185 | |||||||
chr12:51482217 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2173-3570T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482217 | |||||||
chr12:51482746 | C | A | 1 | a0001c0001t0017g0266 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2173-3041C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482746 | |||||||
chr12:51482824 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2173-2963A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482824 | |||||||
chr12:51482848 | A | C | 3 | a0001c0002t0027g0293 a0001c0002t0027g0294 a0001c0002t0044g0295 |
3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2173-2939A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482848 | |||||||
chr12:51482873 | A | T | 1 | a0001c0001t0017g0266 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2173-2914A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51482873 | |||||||
chr12:51483035 | C | T | 50 | a0001c0001t0002g0103 a0001c0001t0004g0025 a0001c0001t0004g0026 others(47): Show |
50 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.2173-2752C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483035 | |||||||
chr12:51483058 | C | G | 1 | a0001c0001t0004g0049 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2173-2729C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483058 | |||||||
chr12:51483232 | C | T | 1 | a0001c0001t0003g0322 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2173-2555C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483232 | |||||||
chr12:51483354 | C | CA | 143 | a0001c0001t0001g0189 a0001c0001t0001g0208 a0001c0001t0001g0211 others(140): Show |
154 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.2173-2421dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51483354 | ||||||
chr12:51483354 | C | CAA | 11 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0106 others(8): Show |
11 | HG00280.hp1 HG01169.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.2173-2422_2173-242 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51483354 | ||||||
chr12:51483354 | CA | C | 7 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2173-2421delA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51483354 | ||||||
chr12:51483356 | A | C | 3 | a0001c0001t0001g0286 a0001c0001t0020g0324 a0001c0001t0020g0325 |
3 | HG01346.hp1 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2173-2431A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483356 | |||||||
chr12:51483470 | C | T | 155 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(152): Show |
166 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.2173-2317C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483470 | |||||||
chr12:51483472 | C | CT | 7 | a0001c0001t0009g0076 a0001c0001t0009g0087 a0001c0001t0009g0089 others(4): Show |
7 | HG02572.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2173-2304dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51483472 | ||||||
chr12:51483552 | A | G | 203 | a0001c0001t0001g0232 a0001c0001t0002g0001 a0001c0001t0002g0002 others(200): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2173-2235A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483552 | |||||||
chr12:51483612 | A | AT | 68 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0022 others(65): Show |
72 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.2173-2167dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51483612 | ||||||
chr12:51483696 | T | G | 1 | a0001c0001t0050g0052 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2173-2091T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483696 | |||||||
chr12:51483721 | G | A | 3 | a0001c0002t0027g0293 a0001c0002t0027g0294 a0001c0002t0044g0295 |
3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2173-2066G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483721 | |||||||
chr12:51483740 | CT | C | 12 | a0001c0001t0001g0215 a0001c0001t0003g0003 a0001c0001t0003g0015 others(9): Show |
15 | HG00673.hp1 HG00735.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.2173-2037delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51483740 | ||||||
chr12:51483859 | G | C | 1 | a0001c0002t0005g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2173-1928G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483859 | |||||||
chr12:51483883 | C | T | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173-1904C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483883 | |||||||
chr12:51483985 | G | A | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173-1802G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483985 | |||||||
chr12:51483994 | T | G | 1 | a0001c0001t0017g0266 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2173-1793T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51483994 | |||||||
chr12:51484071 | T | A | 1 | a0001c0001t0006g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2173-1716T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484071 | |||||||
chr12:51484117 | G | GGGA | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2173-1666_2173-166 others(7): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51484117 | ||||||
chr12:51484211 | G | T | 21 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(18): Show |
25 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.2173-1576G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484211 | |||||||
chr12:51484391 | A | G | 177 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(174): Show |
184 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.2173-1396A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484391 | |||||||
chr12:51484654 | GCTCTCA | G | 5 | a0001c0001t0001g0186 a0001c0001t0001g0256 a0001c0001t0001g0258 others(2): Show |
5 | HG02109.hp2 HG03471.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2173-1128_2173-112 others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr12 | 51484654 | ||||||
chr12:51484686 | A | C | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2173-1101A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484686 | |||||||
chr12:51484888 | A | C | 144 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(141): Show |
151 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.2173-899A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484888 | |||||||
chr12:51484915 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2173-872G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484915 | |||||||
chr12:51484976 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2173-811G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51484976 | |||||||
chr12:51485047 | A | G | 144 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(141): Show |
151 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.2173-740A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51485047 | |||||||
chr12:51485133 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2173-654C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51485133 | |||||||
chr12:51485146 | G | A | 24 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(21): Show |
24 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(21): Show |
intron_variant | MODIFIER | c.2173-641G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51485146 | |||||||
chr12:51485410 | T | C | 1 | a0001c0008t0036g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2173-377T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51485410 | |||||||
chr12:51485477 | T | C | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2173-310T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51485477 | |||||||
chr12:51485617 | T | A | 1 | a0001c0002t0005g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2173-170T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 16/24 | chr12 | 51485617 | |||||||
chr12:51486042 | G | T | 302 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2286+142G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486042 | |||||||
chr12:51486309 | A | G | 30 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(27): Show |
34 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.2286+409A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486309 | |||||||
chr12:51486314 | T | G | 5 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2286+414T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486314 | |||||||
chr12:51486326 | C | G | 8 | a0001c0001t0023g0149 a0001c0001t0040g0147 a0001c0003t0005g0008 others(5): Show |
9 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2286+426C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486326 | |||||||
chr12:51486424 | C | T | 2 | a0001c0002t0010g0152 a0001c0002t0010g0153 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2286+524C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486424 | |||||||
chr12:51486485 | G | A | 144 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(141): Show |
151 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.2286+585G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486485 | |||||||
chr12:51486588 | A | G | 3 | a0001c0002t0027g0293 a0001c0002t0027g0294 a0001c0002t0044g0295 |
3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2286+688A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486588 | |||||||
chr12:51486628 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2286+728G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486628 | |||||||
chr12:51486646 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2286+746C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486646 | |||||||
chr12:51486661 | T | A | 302 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2286+761T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486661 | |||||||
chr12:51486739 | C | T | 172 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(169): Show |
179 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.2286+839C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486739 | |||||||
chr12:51486786 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2286+886C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486786 | |||||||
chr12:51486913 | C | T | 1 | a0001c0001t0043g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2286+1013C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51486913 | |||||||
chr12:51487043 | C | T | 49 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(46): Show |
54 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.2286+1143C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487043 | |||||||
chr12:51487044 | G | A | 1 | a0001c0002t0010g0024 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2286+1144G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487044 | |||||||
chr12:51487193 | C | T | 1 | a0001c0001t0004g0044 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2286+1293C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487193 | |||||||
chr12:51487338 | G | A | 3 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 |
3 | HG01884.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2287-1361G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487338 | |||||||
chr12:51487512 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2287-1187G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487512 | |||||||
chr12:51487513 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2287-1186C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487513 | |||||||
chr12:51487598 | A | G | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2287-1101A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487598 | |||||||
chr12:51487884 | C | T | 1 | a0001c0001t0042g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2287-815C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487884 | |||||||
chr12:51487941 | T | C | 172 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(169): Show |
179 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.2287-758T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51487941 | |||||||
chr12:51488028 | A | T | 1 | a0001c0001t0001g0239 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2287-671A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51488028 | |||||||
chr12:51488139 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2287-560C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51488139 | |||||||
chr12:51488469 | G | A | 46 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(43): Show |
46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.2287-230G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51488469 | |||||||
chr12:51488571 | CT | C | 171 | a0001c0001t0001g0189 a0001c0001t0001g0193 a0001c0001t0001g0262 others(168): Show |
178 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.2287-112delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr12 | 51488571 | ||||||
chr12:51488571 | CTT | C | 8 | a0001c0001t0004g0025 a0001c0001t0004g0065 a0001c0001t0015g0077 others(5): Show |
8 | HG00609.hp1 HG01167.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2287-113_2287-112d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr12 | 51488571 | ||||||
chr12:51488644 | T | C | 1 | a0001c0001t0009g0087 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2287-55T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 17/24 | chr12 | 51488644 | |||||||
chr12:51489002 | G | T | 1 | a0001c0008t0036g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2448+142G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489002 | |||||||
chr12:51489006 | T | G | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2448+146T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489006 | |||||||
chr12:51489302 | A | G | 9 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0106 others(6): Show |
9 | HG00280.hp1 HG01169.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.2449-398A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489302 | |||||||
chr12:51489354 | C | A | 2 | a0001c0001t0004g0049 a0001c0001t0004g0066 |
2 | HG00673.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.2449-346C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489354 | |||||||
chr12:51489408 | T | C | 4 | a0001c0001t0004g0035 a0001c0001t0004g0042 a0001c0001t0004g0050 others(1): Show |
4 | NA18989.hp1 NA18999.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.2449-292T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489408 | |||||||
chr12:51489461 | G | A | 1 | a0001c0001t0004g0035 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2449-239G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489461 | |||||||
chr12:51489518 | C | A | 1 | a0001c0001t0001g0286 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2449-182C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 18/24 | chr12 | 51489518 | |||||||
chr12:51490270 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2700+319T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490270 | |||||||
chr12:51490345 | G | A | 1 | a0001c0001t0023g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2700+394G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490345 | |||||||
chr12:51490415 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2700+464C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490415 | |||||||
chr12:51490433 | C | G | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(135): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.2700+482C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490433 | |||||||
chr12:51490513 | A | G | 1 | a0001c0008t0036g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2700+562A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490513 | |||||||
chr12:51490549 | C | G | 1 | a0001c0001t0007g0275 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2700+598C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490549 | |||||||
chr12:51490562 | C | CA | 21 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0001g0234 others(18): Show |
21 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2700+633dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51490562 | ||||||
chr12:51490562 | CA | C | 9 | a0001c0001t0001g0271 a0001c0001t0002g0141 a0001c0001t0003g0309 others(6): Show |
9 | HG00597.hp1 HG01346.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.2700+633delA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51490562 | ||||||
chr12:51490586 | A | G | 1 | a0001c0001t0011g0199 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2700+635A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490586 | |||||||
chr12:51490587 | T | TGAGGTGG | 67 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0022 others(64): Show |
71 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2700+637_2700+643d others(9): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51490587 | ||||||
chr12:51490655 | G | T | 1 | a0001c0002t0010g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2700+704G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490655 | |||||||
chr12:51490676 | A | G | 1 | a0001c0001t0037g0339 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2700+725A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490676 | |||||||
chr12:51490858 | A | G | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2700+907A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490858 | |||||||
chr12:51490869 | T | G | 1 | a0001c0001t0034g0217 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2700+918T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490869 | |||||||
chr12:51490886 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2700+935T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51490886 | |||||||
chr12:51491015 | A | G | 28 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(25): Show |
28 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.2700+1064A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491015 | |||||||
chr12:51491034 | A | G | 125 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(122): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2700+1083A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491034 | |||||||
chr12:51491037 | G | A | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(135): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.2700+1086G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491037 | |||||||
chr12:51491059 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2700+1108G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491059 | |||||||
chr12:51491098 | A | G | 1 | a0004c0012t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2700+1147A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491098 | |||||||
chr12:51491102 | T | C | 1 | a0001c0001t0043g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2700+1151T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491102 | |||||||
chr12:51491204 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2700+1253G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491204 | |||||||
chr12:51491233 | A | T | 1 | a0001c0006t0002g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2700+1282A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491233 | |||||||
chr12:51491346 | G | A | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.2700+1395G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491346 | |||||||
chr12:51491643 | T | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0268 |
2 | HG01074.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2700+1692T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491643 | |||||||
chr12:51491697 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2700+1746C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491697 | |||||||
chr12:51491737 | G | GCA | 64 | a0001c0001t0002g0001 a0001c0001t0002g0068 a0001c0001t0002g0079 others(61): Show |
66 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.2700+1787_2700+178 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491737 | ||||||
chr12:51491737 | G | GCACA | 18 | a0001c0001t0002g0007 a0001c0001t0002g0093 a0001c0001t0002g0100 others(15): Show |
19 | HG00544.hp2 HG00741.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.2700+1788_2700+178 others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491737 | ||||||
chr12:51491737 | G | GCACACA | 3 | a0001c0001t0002g0081 a0001c0001t0004g0029 a0001c0001t0014g0104 |
3 | HG01978.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2700+1788_2700+178 others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491737 | ||||||
chr12:51491737 | G | GCACACAC others(1): Show |
7 | a0001c0001t0004g0026 a0001c0001t0004g0034 a0001c0001t0004g0050 others(4): Show |
7 | HG02040.hp2 HG02818.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.2700+1788_2700+178 others(12): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491737 | ||||||
chr12:51491737 | G | GCACACAC others(3): Show |
3 | a0001c0001t0004g0054 a0001c0001t0004g0056 a0001c0001t0004g0063 |
3 | HG02027.hp2 NA18946.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2700+1788_2700+178 others(14): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491737 | ||||||
chr12:51491737 | GCAGACAC others(3): Show |
G | 3 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0115 |
3 | HG00639.hp1 HG03490.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2700+1789_2700+179 others(14): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491737 | ||||||
chr12:51491738 | CAG | C | 6 | a0001c0001t0002g0006 a0001c0001t0009g0076 a0001c0001t0009g0087 others(3): Show |
7 | HG00733.hp1 HG00735.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2700+1789_2700+179 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491738 | ||||||
chr12:51491740 | G | C | 129 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(126): Show |
134 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.2700+1789G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491740 | |||||||
chr12:51491740 | G | GAC | 99 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(96): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.2700+1826_2700+182 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | ||||||
chr12:51491740 | G | GACAC | 15 | a0001c0001t0001g0013 a0001c0001t0001g0194 a0001c0001t0001g0209 others(12): Show |
15 | HG00544.hp1 HG01255.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.2700+1824_2700+182 others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | ||||||
chr12:51491740 | G | GACACAC | 7 | a0001c0001t0001g0200 a0001c0001t0001g0276 a0001c0001t0001g0283 others(4): Show |
7 | HG01346.hp1 HG04184.hp2 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.2700+1822_2700+182 others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | ||||||
chr12:51491740 | G | GACACACA others(1): Show |
7 | a0001c0001t0001g0246 a0001c0001t0022g0155 a0001c0001t0037g0339 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2700+1820_2700+182 others(12): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | ||||||
chr12:51491740 | G | GACACACA others(3): Show |
9 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0156 others(6): Show |
10 | HG02055.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2700+1818_2700+182 others(14): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | ||||||
chr12:51491740 | G | GACACACA others(5): Show |
2 | a0001c0002t0010g0024 a0001c0005t0005g0162 |
2 | HG01884.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.2700+1816_2700+182 others(16): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | ||||||
chr12:51491740 | G | GACACACA others(7): Show |
4 | a0001c0002t0005g0165 a0001c0002t0005g0166 a0001c0002t0005g0175 others(1): Show |
4 | HG00558.hp2 NA18941.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.2700+1814_2700+182 others(18): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | ||||||
chr12:51491740 | G | GACACACA others(9): Show |
6 | a0001c0002t0005g0163 a0001c0002t0005g0167 a0001c0002t0005g0168 others(3): Show |
6 | HG02109.hp1 NA18979.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.2700+1812_2700+182 others(20): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | ||||||
chr12:51491740 | G | GACACACA others(11): Show |
5 | a0001c0002t0005g0160 a0001c0002t0005g0161 a0001c0002t0005g0164 others(2): Show |
5 | HG01891.hp1 HG02071.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.2700+1810_2700+182 others(22): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | ||||||
chr12:51491740 | G | GACACACA others(13): Show |
2 | a0001c0002t0005g0171 a0001c0002t0005g0177 |
2 | NA18962.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2700+1808_2700+182 others(24): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51491740 | ||||||
chr12:51491778 | C | CACA | 11 | a0001c0001t0001g0188 a0001c0001t0001g0230 a0001c0001t0001g0272 others(8): Show |
11 | HG01243.hp2 HG01496.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.2700+1827_2700+182 others(7): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491778 | |||||||
chr12:51491778 | C | CACACACA others(4): Show |
1 | a0001c0003t0046g0184 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2700+1827_2700+182 others(15): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491778 | |||||||
chr12:51491778 | C | CACACACA others(6): Show |
1 | a0001c0002t0005g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2700+1827_2700+182 others(17): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491778 | |||||||
chr12:51491778 | C | CACACACA others(10): Show |
1 | a0001c0002t0005g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2700+1827_2700+182 others(21): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491778 | |||||||
chr12:51491939 | A | G | 1 | a0001c0001t0037g0339 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2701-1765A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51491939 | |||||||
chr12:51492086 | G | T | 4 | a0001c0001t0003g0297 a0001c0001t0003g0308 a0001c0001t0003g0310 others(1): Show |
4 | HG00673.hp1 NA19003.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2701-1618G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51492086 | |||||||
chr12:51492426 | A | G | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(135): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.2701-1278A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51492426 | |||||||
chr12:51492523 | C | T | 3 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 |
3 | HG01884.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2701-1181C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51492523 | |||||||
chr12:51492712 | G | T | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.2701-992G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51492712 | |||||||
chr12:51492738 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2701-966A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51492738 | |||||||
chr12:51492775 | A | G | 13 | a0001c0001t0002g0001 a0001c0001t0002g0086 a0001c0001t0002g0093 others(10): Show |
14 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.2701-929A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51492775 | |||||||
chr12:51493034 | A | T | 46 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(43): Show |
46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.2701-670A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51493034 | |||||||
chr12:51493086 | G | A | 3 | a0001c0001t0001g0192 a0001c0001t0001g0222 a0001c0001t0001g0241 |
3 | HG00438.hp2 HG02027.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2701-618G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51493086 | |||||||
chr12:51493094 | T | C | 1 | a0001c0008t0036g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2701-610T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51493094 | |||||||
chr12:51493381 | C | T | 1 | a0001c0001t0037g0339 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2701-323C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51493381 | |||||||
chr12:51493384 | T | TTG | 9 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0125 others(6): Show |
9 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2701-300_2701-299d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51493384 | ||||||
chr12:51493384 | T | TTGTG | 3 | a0001c0001t0016g0046 a0001c0001t0016g0337 a0001c0001t0016g0338 |
3 | NA18943.hp2 NA18963.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2701-302_2701-299d others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr12 | 51493384 | ||||||
chr12:51493543 | T | C | 3 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0025g0031 |
3 | HG01891.hp2 HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2701-161T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51493543 | |||||||
chr12:51493576 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2701-128C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 19/24 | chr12 | 51493576 | |||||||
chr12:51493883 | T | C | 3 | a0001c0001t0002g0079 a0001c0001t0002g0120 a0001c0001t0002g0135 |
3 | HG01993.hp2 HG02273.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.2769+111T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51493883 | |||||||
chr12:51493927 | T | C | 3 | a0001c0002t0005g0173 a0001c0002t0005g0175 a0001c0002t0045g0174 |
3 | NA18955.hp2 NA18988.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2769+155T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51493927 | |||||||
chr12:51493944 | A | G | 21 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(18): Show |
21 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.2769+172A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51493944 | |||||||
chr12:51493945 | T | C | 1 | a0001c0001t0031g0254 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2769+173T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51493945 | |||||||
chr12:51494401 | ATTCTTTT others(2): Show |
A | 3 | a0001c0002t0027g0293 a0001c0002t0027g0294 a0001c0002t0044g0295 |
3 | HG02257.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2770-532_2770-524d others(11): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 51494401 | ||||||
chr12:51494413 | CT | C | 138 | a0001c0001t0001g0196 a0001c0001t0002g0001 a0001c0001t0002g0002 others(135): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.2770-517delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 51494413 | ||||||
chr12:51494503 | C | T | 1 | a0001c0001t0003g0323 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2770-442C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51494503 | |||||||
chr12:51494571 | T | G | 1 | a0001c0001t0053g0088 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2770-374T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51494571 | |||||||
chr12:51494671 | C | T | 1 | a0001c0001t0015g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2770-274C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51494671 | |||||||
chr12:51494702 | T | C | 302 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2770-243T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51494702 | |||||||
chr12:51494823 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2770-122G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 20/24 | chr12 | 51494823 | |||||||
chr12:51495214 | G | T | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(135): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.2943+96G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51495214 | |||||||
chr12:51495470 | C | CT | 49 | a0001c0001t0002g0001 a0001c0001t0002g0081 a0001c0001t0002g0121 others(46): Show |
49 | HG00438.hp1 HG00544.hp2 HG01516.hp2 others(46): Show |
intron_variant | MODIFIER | c.2943+374dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr12 | 51495470 | ||||||
chr12:51495470 | C | CTT | 75 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(72): Show |
80 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.2943+373_2943+374d others(4): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr12 | 51495470 | ||||||
chr12:51495470 | C | CTTT | 12 | a0001c0001t0002g0068 a0001c0001t0002g0071 a0001c0001t0002g0093 others(9): Show |
12 | HG01169.hp2 HG01496.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.2943+372_2943+374d others(5): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr12 | 51495470 | ||||||
chr12:51495470 | CT | C | 120 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.2943+374delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr12 | 51495470 | ||||||
chr12:51495542 | C | G | 57 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(54): Show |
62 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2943+424C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51495542 | |||||||
chr12:51495629 | C | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0022 others(65): Show |
72 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2943+511C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51495629 | |||||||
chr12:51495773 | C | T | 4 | a0001c0001t0001g0246 a0001c0001t0001g0286 a0001c0001t0020g0324 others(1): Show |
4 | HG01346.hp1 HG02257.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2943+655C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51495773 | |||||||
chr12:51495827 | C | T | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2943+709C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51495827 | |||||||
chr12:51495856 | C | T | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2943+738C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51495856 | |||||||
chr12:51496172 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2944-815G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496172 | |||||||
chr12:51496349 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2944-638T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496349 | |||||||
chr12:51496423 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2944-564G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496423 | |||||||
chr12:51496470 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2944-517G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496470 | |||||||
chr12:51496505 | C | G | 2 | a0001c0001t0003g0119 a0001c0001t0003g0129 |
2 | HG03491.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2944-482C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496505 | |||||||
chr12:51496810 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2944-177A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496810 | |||||||
chr12:51496861 | T | C | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2944-126T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496861 | |||||||
chr12:51496937 | G | A | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(135): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.2944-50G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496937 | |||||||
chr12:51496973 | T | A | 7 | a0001c0001t0002g0121 a0001c0001t0009g0076 a0001c0001t0009g0087 others(4): Show |
7 | HG01516.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2944-14T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 21/24 | chr12 | 51496973 | |||||||
chr12:51497483 | T | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0218 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3081+359T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51497483 | |||||||
chr12:51497568 | C | T | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(121): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3081+444C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51497568 | |||||||
chr12:51497801 | G | C | 3 | a0001c0001t0021g0157 a0001c0001t0022g0155 a0001c0001t0022g0156 |
3 | HG02055.hp2 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3081+677G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51497801 | |||||||
chr12:51497864 | C | CAAAAAAA | 156 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(153): Show |
163 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.3081+745_3081+751d others(9): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51497864 | ||||||
chr12:51497864 | C | CAAAAAAA others(1): Show |
11 | a0001c0001t0002g0132 a0001c0001t0004g0035 a0001c0001t0004g0056 others(8): Show |
11 | HG01074.hp1 HG02027.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3081+744_3081+751d others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51497864 | ||||||
chr12:51497886 | G | GA | 125 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(122): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.3081+770dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51497886 | ||||||
chr12:51498039 | T | C | 46 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(43): Show |
46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.3081+915T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498039 | |||||||
chr12:51498060 | A | T | 4 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(1): Show |
4 | HG02109.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3081+936A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498060 | |||||||
chr12:51498138 | T | A | 1 | a0001c0001t0001g0223 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3081+1014T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498138 | |||||||
chr12:51498246 | A | G | 3 | a0001c0001t0003g0014 a0001c0001t0003g0296 a0001c0001t0003g0300 |
4 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3081+1122A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498246 | |||||||
chr12:51498258 | A | G | 172 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(169): Show |
179 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.3081+1134A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498258 | |||||||
chr12:51498467 | A | G | 3 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 |
3 | HG01884.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3081+1343A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498467 | |||||||
chr12:51498509 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3081+1385C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498509 | |||||||
chr12:51498606 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3081+1482C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498606 | |||||||
chr12:51498709 | C | T | 302 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.3081+1585C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498709 | |||||||
chr12:51498755 | C | A | 1 | a0001c0001t0029g0274 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3081+1631C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498755 | |||||||
chr12:51498773 | C | CGGAGGCT others(707): Show |
1 | a0001c0011t0047g0169 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(718): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(707): Show |
2 | a0001c0001t0004g0034 a0001c0001t0004g0061 |
2 | HG04184.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(718): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(707): Show |
3 | a0001c0001t0002g0098 a0001c0001t0023g0075 a0001c0001t0053g0088 |
3 | HG02056.hp1 HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(718): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(706): Show |
2 | a0001c0002t0010g0152 a0001c0002t0010g0153 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(706): Show |
1 | a0001c0002t0005g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(706): Show |
29 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(26): Show |
30 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(706): Show |
3 | a0001c0001t0016g0046 a0001c0001t0016g0337 a0001c0001t0016g0338 |
3 | NA18943.hp2 NA18963.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(706): Show |
41 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(38): Show |
41 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(706): Show |
86 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(83): Show |
92 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(706): Show |
40 | a0001c0001t0001g0276 a0001c0001t0003g0003 a0001c0001t0003g0004 others(37): Show |
45 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(706): Show |
1 | a0001c0001t0009g0091 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(706): Show |
1 | a0001c0001t0021g0157 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(717): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(705): Show |
1 | a0001c0002t0005g0171 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(716): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(705): Show |
1 | a0001c0001t0002g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(716): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(705): Show |
1 | a0001c0001t0040g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(716): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(705): Show |
4 | a0001c0001t0021g0158 a0001c0001t0022g0155 a0001c0001t0022g0156 others(1): Show |
4 | HG01884.hp1 HG02809.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3081+1662_3081+166 others(716): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498773 | C | CGGAGGCT others(704): Show |
1 | a0001c0001t0001g0212 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3081+1662_3081+166 others(715): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498773 | ||||||
chr12:51498812 | G | A | 1 | a0001c0001t0019g0012 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.3081+1688G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498812 | |||||||
chr12:51498850 | A | C | 1 | a0001c0001t0001g0256 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3081+1726A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51498850 | |||||||
chr12:51498879 | C | CA | 122 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(119): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.3081+1775dupA | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498879 | ||||||
chr12:51498879 | C | CAA | 44 | a0001c0001t0001g0022 a0001c0001t0001g0215 a0001c0001t0001g0240 others(41): Show |
49 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.3081+1774_3081+177 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498879 | ||||||
chr12:51498879 | C | CAAA | 146 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(143): Show |
152 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.3081+1773_3081+177 others(7): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498879 | ||||||
chr12:51498879 | C | CAAAA | 24 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0086 others(21): Show |
25 | HG01981.hp2 HG02056.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.3081+1772_3081+177 others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51498879 | ||||||
chr12:51499168 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3081+2044A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51499168 | |||||||
chr12:51499318 | T | C | 302 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.3081+2194T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51499318 | |||||||
chr12:51499540 | A | G | 24 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0015 others(21): Show |
28 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3081+2416A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51499540 | |||||||
chr12:51499624 | T | TAC | 24 | a0001c0001t0002g0001 a0001c0001t0002g0093 a0001c0001t0002g0095 others(21): Show |
26 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.3081+2533_3081+253 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | ||||||
chr12:51499624 | T | TACAC | 27 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0248 others(24): Show |
27 | HG00558.hp2 HG01074.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.3081+2531_3081+253 others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | ||||||
chr12:51499624 | T | TACACAC | 21 | a0001c0001t0001g0013 a0001c0001t0001g0185 a0001c0001t0001g0190 others(18): Show |
22 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.3081+2529_3081+253 others(10): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | ||||||
chr12:51499624 | T | TACACACA others(1): Show |
34 | a0001c0001t0001g0074 a0001c0001t0001g0186 a0001c0001t0001g0204 others(31): Show |
35 | HG00423.hp1 HG00544.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.3081+2527_3081+253 others(12): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | ||||||
chr12:51499624 | T | TACACACA others(3): Show |
27 | a0001c0001t0001g0192 a0001c0001t0001g0202 a0001c0001t0001g0206 others(24): Show |
27 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.3081+2525_3081+253 others(14): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | ||||||
chr12:51499624 | T | TACACACA others(5): Show |
27 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0187 others(24): Show |
30 | HG00140.hp2 HG00597.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.3081+2523_3081+253 others(16): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | ||||||
chr12:51499624 | T | TACACACA others(7): Show |
7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0194 others(4): Show |
7 | HG00642.hp1 HG01192.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.3081+2521_3081+253 others(18): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | ||||||
chr12:51499624 | TAC | T | 41 | a0001c0001t0002g0006 a0001c0001t0002g0078 a0001c0001t0002g0081 others(38): Show |
43 | HG00280.hp1 HG00733.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.3081+2533_3081+253 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | ||||||
chr12:51499624 | TACAC | T | 8 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3081+2531_3081+253 others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | ||||||
chr12:51499624 | TACACACA others(5): Show |
T | 1 | a0001c0001t0002g0131 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3081+2523_3081+253 others(16): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51499624 | ||||||
chr12:51499657 | ACG | A | 3 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0025g0031 |
3 | HG01891.hp2 HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3081+2534_3081+253 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51499657 | |||||||
chr12:51499757 | G | C | 1 | a0001c0002t0010g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3081+2633G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51499757 | |||||||
chr12:51499776 | G | A | 1 | a0001c0001t0003g0314 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3081+2652G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51499776 | |||||||
chr12:51500039 | G | A | 3 | a0001c0002t0005g0173 a0001c0002t0005g0175 a0001c0002t0045g0174 |
3 | NA18955.hp2 NA18988.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3081+2915G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51500039 | |||||||
chr12:51500263 | A | G | 5 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3081+3139A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51500263 | |||||||
chr12:51500276 | C | T | 1 | a0001c0001t0003g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3081+3152C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51500276 | |||||||
chr12:51500413 | CTA | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0218 a0001c0001t0030g0191 |
3 | HG00733.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3081+3291_3081+329 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51500413 | ||||||
chr12:51500695 | C | CT | 48 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(45): Show |
48 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.3082-3325dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51500695 | ||||||
chr12:51500811 | C | A | 2 | a0001c0002t0005g0176 a0001c0002t0005g0177 |
2 | NA18966.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.3082-3218C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51500811 | |||||||
chr12:51500838 | C | A | 2 | a0001c0001t0020g0324 a0001c0001t0020g0325 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3082-3191C>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51500838 | |||||||
chr12:51500850 | C | CT | 131 | a0001c0001t0001g0276 a0001c0001t0002g0001 a0001c0001t0002g0002 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.3082-3166dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51500850 | ||||||
chr12:51500850 | C | CTT | 8 | a0001c0001t0002g0121 a0001c0001t0009g0076 a0001c0001t0009g0087 others(5): Show |
8 | HG01261.hp2 HG01516.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3082-3167_3082-316 others(6): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51500850 | ||||||
chr12:51500860 | T | C | 1 | a0001c0002t0010g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3082-3169T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51500860 | |||||||
chr12:51501071 | C | T | 21 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(18): Show |
21 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.3082-2958C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501071 | |||||||
chr12:51501072 | G | A | 1 | a0001c0001t0025g0028 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3082-2957G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501072 | |||||||
chr12:51501129 | A | G | 172 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(169): Show |
179 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.3082-2900A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501129 | |||||||
chr12:51501315 | C | T | 1 | a0001c0001t0050g0052 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3082-2714C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501315 | |||||||
chr12:51501348 | A | G | 3 | a0001c0001t0021g0157 a0001c0001t0022g0155 a0001c0001t0022g0156 |
3 | HG02055.hp2 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3082-2681A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501348 | |||||||
chr12:51501505 | C | T | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3082-2524C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501505 | |||||||
chr12:51501506 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3082-2523G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501506 | |||||||
chr12:51501517 | T | G | 4 | a0001c0001t0002g0099 a0001c0001t0002g0101 a0001c0001t0002g0328 others(1): Show |
4 | HG00423.hp2 HG00621.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-2512T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501517 | |||||||
chr12:51501544 | T | C | 2 | a0001c0001t0020g0324 a0001c0001t0020g0325 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3082-2485T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501544 | |||||||
chr12:51501846 | G | A | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(135): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.3082-2183G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51501846 | |||||||
chr12:51502048 | A | G | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(135): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.3082-1981A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502048 | |||||||
chr12:51502078 | G | A | 1 | a0001c0001t0004g0336 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3082-1951G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502078 | |||||||
chr12:51502098 | C | T | 81 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(78): Show |
87 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.3082-1931C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502098 | |||||||
chr12:51502164 | A | T | 30 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(27): Show |
31 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(28): Show |
intron_variant | MODIFIER | c.3082-1865A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502164 | |||||||
chr12:51502187 | A | T | 6 | a0001c0003t0005g0008 a0001c0003t0005g0180 a0001c0003t0005g0181 others(3): Show |
7 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3082-1842A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502187 | |||||||
chr12:51502233 | T | TTTTG | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-1780_3082-177 others(8): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51502233 | ||||||
chr12:51502334 | C | T | 2 | a0001c0001t0042g0150 a0001c0001t0043g0151 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-1695C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502334 | |||||||
chr12:51502354 | G | T | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-1675G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502354 | |||||||
chr12:51502364 | T | C | 1 | a0001c0001t0030g0191 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3082-1665T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502364 | |||||||
chr12:51502485 | C | T | 7 | a0001c0001t0006g0005 a0001c0001t0006g0016 a0001c0001t0006g0017 others(4): Show |
8 | HG02895.hp1 HG02922.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.3082-1544C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502485 | |||||||
chr12:51502537 | C | CT | 171 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(168): Show |
178 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.3082-1481dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51502537 | ||||||
chr12:51502569 | C | T | 1 | a0001c0001t0048g0027 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3082-1460C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502569 | |||||||
chr12:51502584 | G | C | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-1445G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502584 | |||||||
chr12:51502636 | G | T | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(135): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.3082-1393G>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502636 | |||||||
chr12:51502773 | C | T | 2 | a0001c0001t0035g0214 a0001c0010t0001g0216 |
2 | HG01192.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3082-1256C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502773 | |||||||
chr12:51502837 | A | AT | 12 | a0001c0001t0001g0228 a0001c0001t0003g0015 a0001c0001t0003g0306 others(9): Show |
13 | HG00735.hp1 HG01261.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.3082-1173dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51502837 | ||||||
chr12:51502837 | AT | A | 90 | a0001c0001t0001g0013 a0001c0001t0001g0185 a0001c0001t0001g0194 others(87): Show |
92 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.3082-1173delT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51502837 | ||||||
chr12:51502864 | AGTCTCGC others(6): Show |
A | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-1161_3082-114 others(17): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51502864 | ||||||
chr12:51502881 | A | G | 302 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.3082-1148A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502881 | |||||||
chr12:51502890 | G | C | 1 | a0001c0002t0005g0167 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3082-1139G>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502890 | |||||||
chr12:51502903 | G | A | 1 | a0001c0001t0042g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3082-1126G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502903 | |||||||
chr12:51502904 | C | T | 1 | a0001c0001t0042g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3082-1125C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502904 | |||||||
chr12:51502905 | C | G | 1 | a0001c0001t0042g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3082-1124C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51502905 | |||||||
chr12:51503040 | C | T | 46 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0029 others(43): Show |
46 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.3082-989C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503040 | |||||||
chr12:51503077 | C | T | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(121): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3082-952C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503077 | |||||||
chr12:51503149 | C | T | 1 | a0001c0001t0003g0315 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3082-880C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503149 | |||||||
chr12:51503229 | T | A | 80 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(77): Show |
86 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3082-800T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503229 | |||||||
chr12:51503232 | A | T | 81 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(78): Show |
87 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.3082-797A>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503232 | |||||||
chr12:51503234 | T | A | 1 | a0001c0001t0001g0221 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3082-795T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503234 | |||||||
chr12:51503247 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3082-782C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503247 | |||||||
chr12:51503342 | G | A | 4 | a0001c0001t0001g0264 a0001c0001t0012g0210 a0001c0001t0012g0265 others(1): Show |
4 | NA18747.hp2 NA18978.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-687G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503342 | |||||||
chr12:51503490 | C | G | 2 | a0001c0001t0042g0150 a0001c0001t0043g0151 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-539C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503490 | |||||||
chr12:51503561 | ATTG | A | 3 | a0001c0001t0021g0157 a0001c0001t0022g0155 a0001c0001t0022g0156 |
3 | HG02055.hp2 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3082-465_3082-463d others(5): Show |
SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 51503561 | ||||||
chr12:51503588 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3082-441A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503588 | |||||||
chr12:51503738 | G | A | 2 | a0001c0001t0014g0020 a0001c0001t0014g0021 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3082-291G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503738 | |||||||
chr12:51503852 | T | C | 4 | a0001c0002t0010g0024 a0001c0002t0010g0152 a0001c0002t0010g0153 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3082-177T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503852 | |||||||
chr12:51503936 | A | G | 1 | a0001c0001t0006g0083 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3082-93A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503936 | |||||||
chr12:51503991 | C | G | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3082-38C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 22/24 | chr12 | 51503991 | |||||||
chr12:51504230 | A | G | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(135): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.3173+110A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504230 | |||||||
chr12:51504281 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3173+161T>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504281 | |||||||
chr12:51504324 | G | A | 138 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(135): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.3173+204G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504324 | |||||||
chr12:51504495 | T | A | 2 | a0001c0001t0002g0070 a0001c0001t0002g0072 |
2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3173+375T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504495 | |||||||
chr12:51504728 | T | G | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.3173+608T>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504728 | |||||||
chr12:51504922 | A | G | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(121): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3173+802A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504922 | |||||||
chr12:51504930 | C | G | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3173+810C>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51504930 | |||||||
chr12:51505420 | A | C | 1 | a0001c0001t0002g0081 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3174-415A>C | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 23/24 | chr12 | 51505420 | |||||||
chr12:51505984 | C | T | 30 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(27): Show |
31 | HG00558.hp2 HG02071.hp2 HG02083.hp1 others(28): Show |
intron_variant | MODIFIER | c.3269+54C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51505984 | |||||||
chr12:51506248 | A | G | 1 | a0001c0001t0007g0275 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3269+318A>G | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506248 | |||||||
chr12:51506321 | C | T | 125 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(122): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.3269+391C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506321 | |||||||
chr12:51506358 | C | T | 1 | a0001c0001t0015g0111 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3269+428C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506358 | |||||||
chr12:51506400 | G | GT | 10 | a0001c0001t0001g0219 a0001c0001t0003g0297 a0001c0001t0009g0076 others(7): Show |
10 | HG00741.hp1 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3269+480dupT | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr12 | 51506400 | ||||||
chr12:51506411 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3269+481C>T | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506411 | |||||||
chr12:51506704 | G | A | 5 | a0001c0001t0021g0157 a0001c0001t0021g0158 a0001c0001t0022g0155 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3270-722G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506704 | |||||||
chr12:51506734 | G | A | 34 | a0001c0002t0005g0159 a0001c0002t0005g0160 a0001c0002t0005g0161 others(31): Show |
35 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.3270-692G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506734 | |||||||
chr12:51506962 | T | A | 1 | a0001c0001t0003g0307 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3270-464T>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51506962 | |||||||
chr12:51507272 | G | A | 7 | a0001c0001t0006g0005 a0001c0001t0006g0016 a0001c0001t0006g0017 others(4): Show |
8 | HG02895.hp1 HG02922.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.3270-154G>A | SLC4A8 | ENSG00000050438.17 | transcript | ENST00000453097.7 | protein_coding | 24/24 | chr12 | 51507272 |